--- a
+++ b/clusters/3009knumclusters/clust_266.txt
@@ -0,0 +1,919 @@
+Provide informed written consent
+Able to provide written informed consent.
+Be willing and able to provide written informed consent/assent for the trial
+Patients must be able to provide written informed consent
+Provide written informed consent
+Inability to provide informed consent
+Subject or subject's representative is willing and able to provide written informed consent
+Patient is able and willing to provide written informed consent
+Provide informed written consent
+Patients or their legally authorized representative must provide written informed consent
+Be willing and able to provide written informed consent for the trial
+Patient must be capable, willing, and able to provide written, informed consent
+Patients must be able to provide written informed consent
+Provide written informed consent
+Willing and able to provide written informed consent.
+Patients must be able to understand and provide written informed consent
+Be willing and able to provide written informed consent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Willing and able to provide written informed consent
+Able to provide informed consent, or have a legal representative able and willing to do so
+COHORT 1: Be willing and able to provide written informed consent / assent for the trial
+COHORT 2: Be willing and able to provide written informed consent/assent for the trial
+Able to provide valid written informed consent
+Able to provide informed consent prior to initiation of study
+Provide written informed consent (Subject or legal representative)
+Subjects must provide written informed consent to participate
+Be willing and able to provide written informed consent for the trial
+Able to understand the nature of this trial and provide written informed consent
+Able to provide confirmed consent
+Ability to provide written informed consent
+Willing and able to provide written Informed Consent and comply with the requirements of the study.
+Must provide written informed consent.
+Able to understand the investigational nature of this study and to provide written consent to participate in it
+Provide written informed consent
+Able to provide written informed consent
+Provide written informed consent
+Patients or their legal representative must be able to provide written informed consent;
+Willingness to provide informed written consent
+Able and willing to provide written informed consent to participate in this study.
+Patients who can provide informed consent
+Patients must provide written consent
+Willing and able to provide written informed consent for the study
+Be willing and able to provide written informed consent for the trial
+Patients unable to provide informed consent
+Able and willing to provide written, signed informed consent (assent as appropriate)
+DONOR: Able and willing to provide written, signed informed consent (assent as appropriate)
+Participant must voluntarily agree to provide written informed consent
+Be willing and able to provide written informed consent for the trial
+Be willing and able to provide written informed consent for the trial
+Are willing and able to provide signed informed consent.
+Provide written informed consent
+Provide informed written consent
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Willing and able to provide written informed consent for the trial
+Able to understand and comply with the requirements of the study and to provide written informed consent or age appropriate assent for pediatric patients.
+Be willing and able to provide written informed consent for the trial
+The subject or their legal guardian be willing and able to provide written informed consent for the trial
+Provide informed consent
+Provide informed written consent
+Patients must be able to provide written informed consent
+Patient refuses or is unable to provide written informed consent
+Willing and able to provide written informed consent to participate in this investigational study.
+Patients must be able to provide informed consent.
+Provide informed written consent
+Provide informed written consent
+Patients must be of appropriate mental capacities with sufficient social support so as to be able to complete required study activities (i.e. diet record, etc) and able to provide written informed consent
+Ability to provide written informed consent
+Patients must be able to understand and provide written informed consent
+Ability to provide written informed consent
+Provide informed written consent
+PART I: Able to understand and provide informed consent
+PART II: Able to understand and provide informed consent
+Patients or their legal representatives must be able to comprehend and provide written informed consent
+Be willing and able to provide written informed consent/assent for the trial.
+Be willing and able to provide written informed consent for the trial and comply with the study visit requirements
+ARM I&II: Patients must be able to provide written informed consent
+Must be willing and able to provide written informed consent
+Provide informed written consent
+The participant (or legally authorized representative, if applicable) must be willing and able to provide written informed consent for the trial
+Provide informed written consent
+Willing and able to provide informed consent.
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent for the trial
+Ability to provide written informed consent.
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Willing and able to provide written informed consent
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial.
+Patients must provide written informed consent.
+Patients must be able to provide written informed consent
+Ability to understand and willing to provide informed consent
+Ability to provide written informed consent for the protocol
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent for the trial
+Provide written informed consent for the follow up protocol.
+Refusal to provide written informed consent
+Patients must provide informed consent
+Must be able and willing to participate in all aspects of the study and provide informed consent prior to study participation.
+Be willing and able to provide written informed consent for the trial.
+Be willing and able to provide written informed consent/assent for the trial
+Provide written informed consent
+Be willing and able to provide written informed consent.
+Be willing and able to provide written informed consent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Provide written informed consent
+Be willing and able to provide written informed consent/assent for the trial.
+Patients must be able to provide written informed consent.
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Willing and able to provide written informed consent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent for the trial
+Provide written informed consent
+Be willing and able to provide written informed consent/assent for the trial.
+Provide written informed consent
+Provide informed written consent
+Patient must be willing and able to provide written informed consent for the trial
+Be willing and able to provide written informed consent for the trial
+Be willing and able to provide written informed consent for the trial
+Provide written informed consent
+Be willing and able to provide written informed consent/assent for the trial
+Provide informed written consent
+Be willing and able to provide written informed consent/assent for the trial
+HEALTHY SUBJECT: Be willing and able to provide written informed consent/assent for the trial
+Must be willing and able to provide written informed consent
+Patients (female or male) must provide informed written consent and must complete all screening assessments as outlined in the protocol
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+The patient or legal guardian must provide written informed consent
+Be willing and able to provide written informed consent for the trial
+Willing to provide informed written consent
+Provide written informed consent
+Be willing and able to provide written informed consent/assent for the study
+Patients are able to understand and provide written informed consent prior to trial participation
+Be willing and able to provide written informed consent/assent for the trial
+Ability to understand and provide informed consent
+Be willing and able to provide written informed consent/assent for the trial
+Provide informed written consent
+Able to provide written informed consent
+Provide informed written consent
+Ability to provide informed consent and adhere to the required follow-up
+Patients or their legally authorized representative must provide written informed consent
+Willing and able to provide informed consent
+Participants must be able to provide informed consent for treatment and trial participation
+Be willing and able to provide written informed consent for the trial
+Able to provide informed consent and be willing to participate in study schedule and events.
+Ability to provide written informed consent
+Willing and able to provide written informed consent.
+Must be able to provide written informed consent before any screening procedures.
+Ability to understand and provide informed consent
+Able to provide written informed consent for the trial
+Patients must be willing and able to review, understand, and provide written consent before study enrollment
+Willing and able to provide informed consent
+Ability to provide signed informed consent and willing and able to comply with all study requirements
+Provide written informed consent
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Willing and able to provide informed consent
+Be willing and able to provide written informed consent for the trial
+Able to provide informed consent and comply with all study protocols
+Able to provide written informed consent.
+Be willing and able to provide written informed consent/assent for the trial
+Willing and able to provide written informed consent
+Willing and able to provide written informed consent for the trial
+Able to provide informed consent
+Competent to provide informed consent
+Able to provide written informed consent
+Provide written informed consent
+Ability to provide informed consent
+Be willing and able to provide written informed consent/assent for the trial
+Provide informed written consent
+Be willing and able to provide written informed consent/assent for the trial
+Adults who are unable to provide informed consent will NOT be enrolled on this study
+Be willing and able to provide written informed consent/assent for the trial
+Ability to provide written informed consent
+Be willing and able to provide written informed consent/assent for the trial
+Provide informed written consent
+Provide informed written consent
+In the judgment of the consenting professional cognitively able to provide informed consent
+Provide written informed consent
+Be willing and able to provide written informed consent/assent for the trial
+Able to provide valid written informed consent.
+Be willing and able to provide written consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Subjects must be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent prior to initiation of any study procedures
+Be willing and able to provide written informed consent/assent for the trial
+Is willing and able to provide written informed consent for the trial.
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent for the trial
+Patient or patient’s legal representative must provide written informed consent
+Be willing and able to provide written informed consent/assent for the trial
+Patients must provide written informed consent
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent for the trial
+Be willing and able to provide written informed consent for the trial
+Willing and able to provide written informed consent
+Subjects must be able to provide written informed consent.
+Provide written informed consent
+Be willing and able to provide written informed consent/assent for the trial; the subject may also provide consent for future biomedical research; however, the subject may participate in the main trial without participating in future biomedical research
+Be willing and able to provide written informed consent for the trial
+Patients must provide written informed consent.
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Ability to provide written informed consent
+Willing and able to provide written informed consent
+Patients or their legally authorized representative must provide written informed consent
+Able and willing to provide informed consent and to comply with the study procedures
+Be willing and able to provide written informed consent/assent for the trial
+Ability to provide informed consent
+Be willing and able to provide written informed consent/assent for the trial
+Willing and able to provide written informed consent
+Willing and able to provide consent
+Must be willing and able to provide written informed consent
+Be willing and able to provide written informed consent for the trial
+Patients or their legally authorized representative must provide written informed consent
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Provide written informed consent (or legal representative)
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Willing and able to provide written informed consent
+Be willing and able to provide written informed consent/assent for the trial
+Ability to provide informed consent.
+Be willing and able to provide written informed consent for the trial
+Be willing and able to provide written informed consent for the trial
+Patients must provide written informed consent prior to any screening procedures
+Ability to understand and provide informed consent
+Ability to understand and provide informed consent
+Be willing and able to provide written informed consent/assent for the trial
+The patient must provide informed consent.
+Willing and able to provide written informed consent
+Provide informed written consent
+Provide informed written consent
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent for the trial
+Willing and able to provide consent
+Be willing and able to provide written informed consent for trial
+Patients must provide informed written consent
+Patients must be willing and able to review, understand, and provide written consent before study enrollment
+Ability to provide written informed consent
+Be willing and able to provide written informed consent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Patients or their legally authorized representative must provide written informed consent
+Patient able and willing to provide informed consent.
+Patients unable to provide informed consent.
+Be willing and able to provide written informed consent/assent for the trial
+Unable to provide written informed consent
+Be willing and able to provide written informed consent for the trial.
+Be willing and able to provide written informed consent/assent for the trial
+Patients or their legally authorized representative must provide written informed consent
+Ability to provide written informed consent.
+Patients must provide written informed consent
+Patients or their legally authorized representative must provide written informed consent
+Patient able to provide written informed consent; parent or guardian of minor patient able to provide written informed consent
+Patient able to provide written informed consent for the long-term follow-up gene therapy study: 2006-0676; parent or guardian of minor patient able to provide written informed consent for the long-term follow-up gene therapy study: 2006-0676
+Inability to provide informed consent
+Be willing and able to provide written informed consent/assent for the trial
+Willing and able to provide informed consent
+Provide informed written consent
+Willingness to provide informed consent to undergo pre- and post-dose biopsy
+Subject must provide written informed consent and be willing and able to comply with all aspects of the protocol
+Patient or legal guardian must provide written informed consent
+Ability to provide written informed consent
+Patients must be able to comprehend and provide written informed consent
+Subject or a legal guardian is able to voluntarily provide written informed consent.
+Patients must provide informed written consent
+Ability to provide written informed consent
+Be willing and able to provide written informed consent/assent for the trial
+Patient or patient’s legal representative able to provide written informed consent
+Be willing and able to provide written informed consent for the trial
+Either the subject or the subject’s legal representative must be willing and able to provide written informed consent for the trial
+Patients or their legally authorized representative must provide written informed consent
+Patients or their legally authorized representative must provide written informed consent
+Is willing and able to provide written informed consent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Willing and able to provide written informed consent prior to initiation of any study-related procedures
+Patients must provide written informed consent
+Ability to provide informed consent for participation
+Provide informed written consent
+Be willing and able to provide written informed consent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Patients must provide written informed consent
+All patients must be willing and capable to provide informed consent to participate in the protocol
+Patient must be capable, willing, and able to provide written, informed consent
+Be willing and able to provide written informed consent/assent for the trial
+Able to provide written informed consent
+Provide written informed consent for the trial
+Patients or their legally authorized representative must provide written informed consent
+Be willing and able to provide written informed consent/assent for the trial
+Patient or patient’s legal representative, parent(s), or guardian able to provide written informed consent
+Provide informed written consent
+Must provide written informed consent
+Patients must be willing and able to review, understand, and provide written consent before starting therapy
+Able to understand and to provide voluntarily informed consent
+Patients must be able to provide informed consent
+Patient or patient’s legal representative, parent(s) or guardian able to provide written informed consent
+Patients must be able to provide written informed consent
+Subjects must be able to provide written informed consent
+Ability to provide written, informed consent
+Participant must provide informed consent
+Patients must provide written informed consent
+Provide informed written consent
+Patients 18 years or older will provide written consent. A parent or legal guardian of a patient <18 years of age will provide informed consent and patients 11 to 18 years of age will provide written assent or as per participating institutional policy.
+Able and willing to provide written informed consent and to comply with the study protocol
+Able to provide written informed consent
+Patients must agree to participate and be able to understand and provide informed consent to participate in the trial
+For Phase I and II: Patients must provide written informed consent.
+Ability to understand and provide informed consent
+Patient must be able to provide written informed consent
+Patients must be able to provide informed consent
+Willing and able to comply with the study procedures and provide written informed consent to participate in the study
+Patients must be willing and able to review, understand, and provide written consent before starting therapy
+Ability to provide informed consent
+Must be willing and able to provide written informed consent
+Subjects who provide written informed consent to participate in the study
+COHORTS 1 AND 2: HEALTHY VOLUNTEERS: Ability of subject to understand and provide written informed consent
+Patients must be able to provide written-informed consent
+Patients must be able to provide informed consent
+Eligibility criteria specific to the control arm:\r\n* Participants must be willing and able to provide written informed consent/assent for the control arm of the INdividualized Screening trial of Innovative Glioblastoma Therapy (INSIGhT) trial
+Willingness to provide written informed consent for the study.
+Provide written informed consent prior to any study related procedure.
+Provide informed written consent
+Provide written informed consent to participate on the study
+Ability to provide written informed consent
+Patients must be able to provide informed consent
+Patients must be able to provide informed consent
+Patients must be able to provide informed consent
+All patients must be willing and capable to provide informed consent to participate in the protocol
+Patients must provide written consent
+Inability to provide informed consent.
+Ability of patient to provide informed consent
+Be willing and able to provide written informed consent/assent for the trial
+Willing and able to provide written informed consent.
+Provide written informed consent
+Provide written informed consent
+Provide written informed consent
+Participant must be able to provide written Informed Consent
+Participant unwilling to provide written informed consent
+Patients are not able to provide written informed consent to study participation
+Be willing and able to provide written informed consent
+Ability to provide informed consent.
+Able to understand and willing to provide written informed consent.
+Ability to understand the requirements of the study, provide written informed consent.
+Ability to provide written informed consent
+Able to understand and provide informed consent
+Patients must provide written informed consent.
+Provide written informed consent
+Ability to provide written informed consent
+Ability to provide written informed consent and to understand and comply with the requirements of the study
+Be willing and able to provide written informed consent for the trial
+Able to provide written informed consent
+Can provide informed consent
+Able and willing to provide informed consent
+Able to provide signed, written informed consent
+Patient able to provide written informed consent.
+Patient able to provide written informed consent for the long-term follow-up (LTFU) gene therapy study.
+Provide written informed consent
+Must be able to provide informed consent.
+Provide written informed consent
+Be willing and able to provide written informed consent for the trial
+Be willing and able to provide written informed consent for the trial.
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Provide informed written consent
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Ability to provide written informed consent
+Able to provide informed consent
+Patients must be able to provide written informed consent
+Subjects or their legal representative must be able to understand and provide written informed consent
+Provide informed written consent
+Willing and able to provide written informed consent for the trial
+Be willing and able to provide written informed consent for the trial
+Inability to understand or provide informed consent
+Patients must be able to provide written informed consent
+Be willing and able to provide written informed consent for the trial
+Willing and able to provide written informed consent for voluntary participation in the trial
+Provide informed written consent
+ARM A: Ability to provide informed written consent
+ARM B: Ability to provide informed written consent
+Ability to provide informed consent
+Ability to provide informed consent
+Patients must provide informed written consent
+Provide written informed consent
+Be willing and able to provide written informed consent for the trial
+Ability to provide written informed consent
+Ability to provide informed consent
+Be willing and able to provide written informed consent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Inability to provide informed consent
+Ability and willingness to provide informed consent to participate in this study
+Provide informed written consent
+Ability to provide informed consent
+Ability to provide informed consent
+Be willing and able to provide written informed consent/assent for the trial
+Ability to understand and provide voluntary written informed consent
+Willingness to provide informed consent
+Provide written informed consent
+Patients must be able to provide written informed consent
+Provide written informed consent
+Be willing and able to provide written informed consent/assent for the trial
+Willing and able to provide written informed consent
+Be willing and able to provide written informed consent/assent for the study
+Patients must provide written informed consent prior to any screening procedures
+They must be able to provide informed consent
+Ability to provide informed consent
+Able to provide informed consent
+Patients must provide verbal and written informed consent to participate in the study
+Ability to provide written informed consent
+Subjects or their legal representatives must be able to provide written informed consent.
+Patients must provide written informed consent.
+Able and willing to provide written informed consent
+All patients must be willing and capable to provide informed consent to participate in the protocol
+Able to provide informed consent
+Patient willing and able to provide written informed consent
+Patients or their legal representative (if the patient is < 18 years old) must be able to read, understand and provide written informed consent to participate in the trial.
+Willingness to provide written informed consent for the study.
+Willing to provide written informed consent
+Provide informed written consent
+Ability to provide informed written consent
+Patients must provide written informed consent prior to any screening procedures
+Patients, or appropriate designee, must be able to provide informed consent
+Patients must be able to provide written informed consent
+Able and willing to provide written informed consent to participate in the study
+Able and willing to provide written informed consent and to comply with the study protocol
+Participant must voluntarily agree to provide written informed consent.
+Be willing and able to provide written informed consent for the trial and comply with the study visit requirements
+Willing and able to provide informed consent
+Patients must provide written informed consent
+Be willing and able to provide written informed consent
+Be willing and able to provide written informed consent for the trial.
+DONOR: Willing and able to provide informed consent
+Be willing and able to provide written informed consent/assent for the trial
+Able to provide written informed consent
+Be willing and able to provide written informed consent for the trial
+Patients must provide written informed consent
+Must be willing and able to provide written informed consent
+Provide written informed consent
+Ability to understand and provide written informed consent
+Provide written informed consent
+Able to provide written informed consent and to follow protocol requirements.
+Subject or Authorized Representative is unable to provide informed consent.
+Ability to provide informed consent
+Must be willing and able to provide written informed consent
+Ability to provide informed consent
+Ability and willingness to provide written informed consent, and to comply with the requirements of the protocol
+Willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent for the trial
+Patients or their legally authorized representative must provide written informed consent
+Provide informed written consent
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial; consent may be obtained by legally authorized representative (LAR) according to the protocol
+Willing and able to provide informed written consent
+Provide informed written consent
+Patients or their legally authorized representative must provide written informed consent
+Ability to provide informed consent
+Patient or patient’s legal representative able to provide written informed consent
+Ability and willingness to provide informed consent
+Be willing and able to provide written informed consent/assent for the trial
+Patients or their legally authorized representative must provide written informed consent
+Able and willing to provide written informed consent
+Either the subject or his/her legally authorized representative be willing and able to provide written informed consent for the trial
+Be willing and able to provide written informed consent/assent and authorization permitting study-related release of personal health information
+Be willing and able to provide written informed consent/assent for the trial
+Able to provide informed written consent
+Be willing and able to provide written informed consent for the trial
+Provide written informed consent
+Provide informed written consent
+Be willing and able to provide written informed consent/assent for the trial
+All patients must be willing and capable to provide informed consent to participate in the protocol
+Ability to provide written informed consent and comply with study requirements
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Ability to provide informed consent
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Provide informed written consent
+Be willing and able to provide written informed consent/assent for the trial
+Provide informed written consent
+Provide informed written consent
+Patients, or appropriate designee, must be able to provide informed consent
+Provide informed written consent
+Ability to provide informed written consent
+Subject is able to provide written informed consent.
+Able to provide informed written consent
+Adults who are unable to provide informed consent will NOT be enrolled on this study
+Patients must provide informed consent
+Willing and able to provide informed consent
+Patient should be able to provide informed consent
+Patients must provide verbal and written informed consent to participate in the study
+Patients must provide written informed consent prior to any registration on study
+Ability to provide written informed consent
+Ability and willingness to provide written informed consent
+COHORT A: The subject must be willing and able to provide informed consent
+COHORT B: The subject must be willing and able to provide informed consent
+Unable to provide informed consent
+Ability to provide informed consent
+Patient must be capable, willing, and able to provide written, informed consent
+For adult patient, the patient is able to provide informed consent. For pediatric patient, a parent is able to provide informed consent.
+Patient willing and able to provide written informed consent for the trial
+Provide informed written consent
+Provide written informed consent
+Provide informed written consent
+Patients must be able to provide written informed consent
+Patients must be willing and able to review, understand, and provide written consent before starting therapy
+Able to provide written informed consent
+Provide informed written consent
+Ability and willingness to provide written informed consent
+Provide informed written consent
+Patients must provide informed written consent
+Ability to provide informed written consent
+Inability to provide informed consent
+Willing and able to provide informed consent
+Willing and able to provide written informed consent
+Able and willing to provide written informed consent.
+Patients willing and able to review, understand, and provide written consent before starting therapy
+Able to provide written consent
+Cognitively impaired patients who cannot provide informed consent
+Provide informed written consent
+Patients who provide written informed consent for participation in this trial
+Able to provide informed consent and follow protocol requirements.
+Inability to provide informed consent.
+Patients must be able to provide informed consent
+Provide informed written consent
+Provide written informed consent
+Able to provide written, informed consent
+Provide informed consent
+Inability to provide informed consent
+All patients must be willing and capable to provide informed consent to participate in the protocol
+Patients must be willing and able to provide signed informed consent and comply with the study protocol.
+Ability to provide written informed consent
+Patient or guardian willing and able to provide informed consent.
+Inability to provide informed consent
+Ability to provide informed consent
+Provide written informed consent
+Ability to provide informed consent.
+Be willing and able to provide written informed consent/assent for the trial
+Ability to provide informed consent
+Understands the potential risks and benefits of study participation and is willing to provide written informed consent.
+Patients must be able to provide written informed consent
+Ability to understand and provide informed consent
+Able to provide informed consent for the study
+Patients must be able to provide informed consent
+Patients must provide written informed consent
+Willing and able to provide written Informed Consent and adhere to study procedures.
+Patients must be willing and able to review, understand, and provide written consent before starting therapy
+Inability to provide informed consent
+Provide informed written consent
+Patients must provide informed consent
+Patients or their legal representatives must be able to read, understand, and provide informed consent to participate in the trial
+Provide informed written consent
+Subjects must be able to understand the potential risks and benefits of the study and must be able to read and provide written, informed consent for the study
+Be willing and able to provide written informed consent/assent for the trial
+Willingness to provide written informed consent for the study.
+Patients must be able to provide written informed consent
+Willing and able to provide informed consent
+Provide written informed consent.
+Subjects must be able to understand the potential risks and benefits of the study and must be able to read and provide written, informed consent for the study
+Willing and able to provide written informed consent
+Provide informed written consent
+Patients unable to provide informed consent
+Able to provide written informed consent.
+Patients, or appropriate designee, must be able to provide informed consent
+At least 18 years of age and willing and able to provide informed consent.
+Ability to provide written informed consent
+Willing and able to provide informed consent
+Able to understand and have the ability to provide written consent
+Patients must provide written informed consent.
+Willingness and ability to provide written informed consent and to comply with the protocol requirements
+Able to provide informed consent
+Able to provide written informed consent and to follow protocol requirements
+Patient, or his/her legally authorized representative, is able to understand and provide informed consent.
+Willing and able to provide written informed consent.
+Provide written informed consent prior to any screening procedures
+Patients or their legally authorized representative must provide written informed consent
+Ability to understand and provide informed consent
+Ability to provide informed consent
+Inability to provide informed consent
+Provide written informed consent prior to any screening procedures
+Subject is able to voluntarily provide written informed consent.
+Provide informed written consent
+Subjects between 12 and 35 years of age, inclusive, at the time of consent/assent, and able to provide written consent/assent, if applicable.
+Willing and able to provide written informed consent
+Provide written informed consent
+Must be willing and able to provide written informed consent and comply with the protocol and study procedures
+Provide informed written consent
+Ability to provide informed consent
+Ability to provide informed written consent
+Able to provide informed consent, child assent with parental consent or surrogate consent when applicable
+4. Patient is able and willing to provide written informed consent to participate in the study.
+Ability to provide written informed consent
+Patients must be able to provide written informed consent
+Subject or subject's representative is willing and able to provide written informed consent
+Willing and able to provide informed consent;
+Provide informed written consent
+Ability to provide informed consent
+Provide informed written consent
+Provide written informed consent
+Inability to provide informed consent
+Able to provide written informed consent
+Provide written informed consent and willing to comply with protocol requirements.
+Ability to understand and provide written informed consent to participate in this study.
+Willing and able to provide written informed consent.
+Inability to provide adequate informed consent
+Able to understand and provide written informed consent
+Patients must be able to provide informed consent
+Ability to provide written informed consent
+Willing and able to provide informed consent
+Be willing and able to provide written informed consent/assent for the trial
+Provide informed written consent
+Patients must provide written informed consent
+Provide informed written consent
+Age 18 years or older and willing and able to provide informed consent;
+Have ability to provide full written consent
+Able to understand and provide written informed consent
+Patients or their legally authorized representative must provide written informed consent
+Ability to provide informed written consent
+Able to provide written informed consent, and agree to practicing 2 forms of birth control during the study
+Provide informed written consent
+Provide written informed consent
+Provide informed written consent
+Be able to provide written informed consent
+Both must provide informed consent
+Able to provide informed consent
+Unable to provide consent
+Able to read either English or Spanish and able to provide written (via paper), verbal consent or on-line informed consent
+Able to provide written informed consent
+Be able to provide informed consent
+Patient/caregiver can provide informed consent
+Patient/partner is able to provide informed consent
+Able to comprehend and provide informed consent
+Able to provide informed consent
+Patient able to provide his/her own written informed consent and speak English
+Inability to provide informed consent
+Unable to provide informed consent
+Patients must provide written informed consent prior to any screening procedures
+Able to provide written informed consent
+Be willing and able to provide written informed consent/assent for the trial
+Patients unable to understand the research protocol and/or provide informed consent
+The ability to provide informed consent
+PATIENT & PARTNER: Able to provide informed consent
+Provide written informed consent
+Able to provide informed consent
+Are able to provide voluntary, written consent
+Inability to provide a fully informed consent.
+Must be able to provide own consent
+PATIENTS AND CAREGIVERS: Able to provide informed consent.
+Able to provide informed consent
+PROVIDER ELIGIBILITY: The participant is willing to provide informed consent in English
+Unwilling to provide informed consent
+Phase I: Able to provide informed consent
+Phase II: Able to provide informed consent
+Patients who are unable to provide informed consent in English will be excluded
+Able to provide informed consent
+Cannot provide meaningful informed consent
+Patients unable to provide informed consent
+Ability to provide informed consent
+In the judgment of the consenting professional cognitively able to provide informed consent
+In the judgment of the consenting professional cognitively able to provide informed consent
+Able and willing to provide informed consent
+PATIENTS AND PARTNERS: Able to provide consent
+Ability to provide informed consent
+Adults who are able to provide informed consent
+Willing and able to provide informed consent
+Willing and able to provide informed consent
+Not willing and able to provide informed consent
+Can provide informed consent (e.g., no cognitive impairment)
+CAREGIVER: Can provide Informed consent
+Must provide written informed consent
+Psychiatric disorder which would render the subject unable to provide informed consent
+Subject is willing to provide written informed consent
+Patient or patient’s legal representative(s) is/are able to provide written informed consent to participate
+Ability to provide informed written consent
+Unable to provide informed consent
+Subject is able to provide informed consent
+Are unable to provide informed consent
+Ability and Willingness to provide informed consent
+Unwilling to provide informed consent
+Able to provide informed consent
+Be willing to provide written informed consent to participate in the study which includes several clinical evaluations, provide access to medical records/primary care physician (PCP), and allow all interviews and PSST therapy sessions to be audiotaped.
+Provide written informed consent
+Capable and willing to provide Informed consent
+FCGs: Able to provide informed consent
+PATIENTS: Not able to provide informed consent
+Able to provide informed consent
+Able and willing to provide written consent
+Patients unable to provide informed consent
+Patients must be able to provide written informed consent
+Willing and able to provide informed consent
+Not willing and able to provide informed consent
+Patients must be able to provide informed consent
+Provide written informed consent
+Provide written informed consent prior to screening
+Be able to provide written informed consent
+Able to provide informed consent
+Willing to provide informed written consent
+PHASE I: Able to provide meaningful informed consent
+PHASE II: Able to provide meaningful informed consent
+Ability to provide informed written consent
+Inability to provide informed consent
+Inability to provide informed consent
+Willing and able to provide signed, informed consent
+Willing and able to provide written informed consent
+Subjects able to provide informed consent
+Able to provide written informed consent and authorization for release of health information
+Able and willing to provide consent (both)
+Ability to provide informed consent
+Able to provide written informed consent
+Inability to provide informed assent/permission/consent
+Ability to provide informed written consent
+Can provide informed consent
+Ability to provide informed written consent
+Inability to provide informed consent
+PATIENT: Be able and willing to provide informed consent
+Unable to provide informed consent
+Able and willing to provide informed consent
+Provide informed written consent
+Patients must be willing and able to review, understand, and provide written consent
+Ability to provide written informed consent
+Patients willing and able to review, understand, and provide written consent
+Provide informed written consent
+Unwilling to provide informed consent
+Unwilling to provide informed consent
+Patients willing and able to review, understand, and provide written consent before starting therapy
+Unwilling to provide informed consent
+Patients who are willing and able to review, understand, and provide written consent
+Willing and able to provide, signed informed consent
+Provide informed written consent
+Able to provide informed consent
+Inability to provide informed consent
+The subject must be willing and able to provide informed consent
+Able to provide informed consent
+Patients must provide written informed consent prior to any screening procedures
+Patients must provide written informed consent to participate in the study
+Able to provide informed consent
+Cognitively able and willing to provide consent
+Provide informed written consent
+Patients must be willing and able to provide a written informed consent
+Unable to provide informed consent
+Able and willing to provide written informed consent
+Provide informed consent
+Patients who cannot provide a valid consent
+Subjects unable to provide consent
+Patients can provide informed consent
+Be able to provide informed consent in English or Spanish
+Able to provide informed consent in English
+Unable to provide informed consent
+CONTROL (HEALTHY) GROUP: Unable to provide informed consent
+Participant is unable to provide informed consent
+Ability to provide informed written consent
+Unable to provide informed consent
+Inability to provide informed consent
+Willing to provide informed consent/assent for study participation
+Willing to provide informed consent/assent for study participation
+Unable to provide informed consent
+Subjects willing and able to provide consent to participating in the study
+Able to provide verbal consent
+Able to provide informed consent
+Patients must be willing and able to provide written informed consent for the trial
+Willing and able to provide written informed consent
+Ability to read and provide written informed consent
+Willingness to provide written informed consent
+Provide written informed consent.
+Able to provide informed consent to participate in the study
+Unable to provide informed consent
+Able to understand and willing to provide informed consent for the RPFNA’s and study participation
+Unable to provide informed consent
+Inability to provide informed consent
+Able to provide informed consent
+Have the ability to provide informed consent in English
+FOLLOW UP ASSESSMENTS: Have the ability to provide informed consent in English
+Patients must be able to provide written informed consent
+Ability to provide written informed consent
+Inability to provide informed consent
+Able to provide informed consent
+Understand the study procedures and able to provide informed consent
+Patients who are willing and capable to provide informed consent
+Able and willing (or have legal representative) to understand the study and provide consent
+Inability to provide informed consent (and assent, if subject is under the age of 18)
+the ability to comply with the study protocol and provide informed consent
+Capable and willing to provide informed consent
+Patient must be able and willing to provide written informed consent
+The patient is willing and able to provide informed consent.
+Patients unable to provide informed consent
+Be willing and able to provide written informed consent/assent for the trial
+Able to provide legally effective informed consent
+Provide written informed consent for the study
+Are able to provide informed consent
+Are unable to provide informed consent
+Patients must be able to provide written informed consent
+Able to provide written informed consent and willing to comply with protocol requirements
+Able to provide written consent
+Patients must be capable and willing to provide informed consent
+Inability to provide informed consent on their own behalf
+Unable to provide written consent
+Willingness to participate in the study and able to provide informed consent
+Patients must be able to provide informed consent
+Able to provide written consent
+Patients must be capable and willing to provide informed consent.
+Able to provide informed consent and follow the study guidelines
+Patient able and willing to provide informed consent
+Patient is able to provide written informed consent prior to study registration
+Patients must be able to provide written informed consent
+Cannot provide written informed consent
+Patients must be able to provide written informed consent
+Cannot provide written informed consent
+Ability to provide informed consent
+Able to provide informed consent
+Able to provide written informed consent
+Able to provide written consent
+Able to provide written consent
+Unable to provide informed consent
+Subject/legal representative willing and able to provide written informed consent
+Able to provide informed consent
+Provide informed written consent if >= 18 years; if < 18 years, provide informed written assent and parent or legal guardian provide informed written consent
+Provide written informed consent
+Refusal to provide informed consent
+Patients must provide written informed consent
+Females unable to provide informed consent
+Subjects unable to provide own consent are not eligible
+Subject and/or guardian is able to provide written informed consent prior to study registration
+Able to read or understand and provide informed consent
+Patient and/or guardian is able to provide written informed consent prior to study registration
+Patient and/or guardian is able to provide written informed consent prior to study registration
+Patient and/or guardian is able to provide written informed consent prior to study registration
+Able to provide written informed consent
+Patients must be able to provide written informed consent
+Cannot provide written informed consent
+Able to provide written informed consent.
+Ability to provide informed consent
+Inability to provide informed consent
+HEALTHY VOLUNTEERS: Patient is willing to provide informed consent
+HCC PATIENTS: Patient is willing to provide informed consent
+Able to provide written consent
+Able to provide written informed consent
+Inability to provide written informed consent
+Participant willing to provide a written informed consent
+Willing and able to provide written informed consent
+Patient and/or legal guardian able and willing to provide informed consent
+Patient unable to provide informed consent
+Patients must be able to provide written informed consent
+Those who are pregnant, claustrophobic, or unable to provide informed consent
+Are able to provide informed consent
+Are unable to provide informed consent
+Ability to provide written informed consent
+Subjects unable to provide own consent are not eligible
+Unable to provide informed consent
+Able to provide informed consent
+Ability to provide informed consent
+Inability to provide informed consent
+Unable to provide consent
+Patient and/or guardian is able to provide written informed consent prior to study registration
+Subjects must to able to provide informed written consent prior to study entry
+Provide informed written consent
+Patients must provide informed written consent
+Willing and able to provide informed written consent
+Be willing and able to provide written informed consent for the trial
+Patients must provide written informed consent
+The patient must be willing and able to provide informed consent
+Patients must be able to provide written informed consent
+Cannot provide written informed consent
+Willing and able to provide a written informed consent
+Must be able to provide a written informed consent
+Inability to provide informed consent
+Unable to provide informed consent
+Patients unable to provide informed consent
+Ability to provide written, informed consent.
+Able to provide written informed consent
+Able to provide written informed consent and willing to comply with protocol requirements
+Willing and able to provide informed consent
+Are able to provide informed consent
+Are unable to provide informed consent
+Unable to provide informed consent
+Be willing and able to provide informed consent
+NORMAL VOLUNTEERS: Be willing and able to provide informed consent
+Provide written informed consent and willing to comply with protocol requirement
+Able to provide informed consent
+Able to understand the experimental nature of the study and provide informed consent
+Provide informed written consent
+Willing and able to provide written informed consent
+Subjects are required to be willing and able to provide written informed consent
+Participants who are not able to understand or provide written informed consent
+Ability to provide informed consent
+Ability to provide written informed consent obtained prior to participation in the study
+Able to provide informed consent
+Ability to provide consent
+PATIENTS: The ability to provide informed consent
+Able to provide informed consent to participate in the study
+Must be able to provide informed consent
+Willing and able to provide informed consent and fill out demographic, disease, and pain assessment questionnaires
+Can provide informed consent
+Be willing and able to provide written informed consent.
+Patients unable to provide informed consent
+Men who are unable to provide their own informed consent
+Patients must be able and willing to provide written informed consent prior to any study related procedure.
+Able to provide written informed consent.
+Ability and willingness to provide written informed consent
+Able to provide written informed consent
+Be willing and able to provide written informed consent/assent for the trial
+Participants must voluntarily agree to provide written informed consent.
+Be willing and able to provide written informed consent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial
+Be willing and able to provide written informed consent/assent for the trial