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+Able to provide informed consent prior to initiation of study
+Able to provide confirmed consent
+Patients must be able to provide informed consent.
+PART I: Able to understand and provide informed consent
+PART II: Able to understand and provide informed consent
+DONOR: Able to provide informed consent for the donation process per institutional standards.
+Participants must be able to provide informed consent for treatment and trial participation
+Able to provide informed consent and comply with all study protocols
+Able to provide informed consent
+In the judgment of the consenting professional cognitively able to provide informed consent
+The patient must provide informed consent.
+Patients must be able to provide informed consent
+Participant must provide 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
+Patients must be able to provide informed consent
+Patients must be able to provide informed consent
+Able to understand and provide informed consent
+Must be able to provide informed consent.
+Able to provide informed consent
+Willingness to provide informed consent
+They must be able to provide informed consent
+Able to provide signed, informed consent
+Able to provide informed consent
+Able to provide informed consent
+Patients, or appropriate designee, must be able to provide informed consent
+Participant is able to provide signed informed consent
+Patients, or appropriate designee, must be able to provide informed consent
+Patient should be able to provide informed consent
+For adult patient, the patient is able to provide informed consent. For pediatric patient, a parent is able to provide informed consent.
+Cognitively impaired patients who cannot provide informed consent
+Able to provide informed consent and follow protocol requirements.
+Patients must be able to provide informed consent
+Able to provide informed consent for the study
+Patients must be able to provide informed consent
+Patients, or appropriate designee, must be able to provide informed consent
+Able to provide informed consent
+Able to provide informed consent, child assent with parental consent or surrogate consent when applicable
+Patients must be able to provide informed consent
+Able to provide informed consent
+Be able to provide informed consent
+Patient/partner is able to provide informed consent
+Able to comprehend and provide informed consent
+Able to provide informed consent
+PATIENT & PARTNER: Able to provide informed consent
+Able to provide informed consent
+Must be able to provide own consent
+PATIENTS AND CAREGIVERS: Able to provide informed consent.
+Able to provide informed consent
+Phase I: Able to provide informed consent
+Phase II: Able to provide informed consent
+Able to provide informed consent
+Cannot provide meaningful 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
+PATIENTS AND PARTNERS: Able to provide consent
+Adults who are able to provide informed consent
+Subject is able to provide informed consent
+Able to provide informed consent
+FCGs: Able to provide informed consent
+PATIENTS: Not able to provide informed consent
+Able to provide informed consent
+Patients must be able to provide informed consent
+Able to provide informed consent
+PHASE I: Able to provide meaningful informed consent
+PHASE II: Able to provide meaningful informed consent
+Subjects able to provide informed consent
+Able to provide informed consent
+Able to provide informed consent
+Able to provide informed consent
+Able to provide informed consent in English
+Able to provide verbal consent
+Able to provide informed consent
+Able to provide informed consent to participate in the study
+Able to provide informed consent
+Able to provide informed consent
+Understand the study procedures and able to provide informed consent
+Able to provide legally effective informed consent
+Are able to provide informed consent
+Patients who in the judgment of the investigators and/or consenting professional, are able to understand the purpose of the study and provide informed consent will be included
+Willingness to participate in the study and able to provide informed consent
+Patients must be able to provide informed consent
+Able to provide informed consent and follow the study guidelines
+Able to provide informed consent
+Able to provide informed consent
+Able to read or understand and provide informed consent
+Are able to provide informed consent
+Able to provide informed consent
+Are able to provide informed consent
+Able to provide informed consent
+Able to provide informed consent
+Able to provide informed consent (Pre-pilot phase, Arms -, PCS study)
+Able to provide informed consent to participate in the study
+Must be able to provide informed consent