Patients must have signed an approved informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization
Ability to provide written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization
Subject must be fully informed about their illness and the investigational nature of the study protocol (including foreseeable risks and possible side effects) and must sign and date an IRB [Institutional Review Board]-approved Informed consent Form [ICF] (including Health Insurance Portability and Accountability Act authorization, if applicable) before performance of any study specific procedures or tests.
Ability to provide written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization. This will be assessed by the consenting physician using general questions as outlined in Etchells  publication titled Assessment of Patient Capacity to Consent to Treatment. These are general conversation based questions that assess the patients ability to understand the medical problem, proposed treatment, alternatives to proposed treatment, and understand the consequences of the medical choices
Ability to provide written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization
Ability to provide written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization
Ability to provide written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization
Signed an institutional review board (IRB)-approved informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization
Subjects must sign a written informed study consent and Health Insurance Portability and Accountability Act (HIPAA) consent prior to performance of study-specific procedures or assessments and must be willing to comply with treatment and follow up
Signed written informed consent including Health Insurance Portability and Accountability Act (HIPAA) according to institutional guidelines
Patients must have signed an approved informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization
Subjects must sign and date an Institutional Review Board-approved informed consent form (including Health Insurance Portability and Accountability Act authorization, if applicable) before performance of any study-specific procedures or tests
Subject must sign and date an Institutional Review Board-approved informed consent form (including Health Insurance Portability and Accountability Act authorization, if applicable) before performance of any study-specific procedures or tests.
Participants must sign a written informed consent and Health Insurance Portability and Accountability Act (HIPAA) consent prior to performance of study-specific procedures or assessments and must be willing to comply with treatment and follow up
Subject must have read, understood, and provided written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization after the nature of the study has been fully explained
Subject must have read, understood, and provided written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization after the nature of the study has been fully explained
Provision of written informed consent approved by the Institutional Review Board (IRB) or Independent Ethics Committee (IEC) with privacy language in accordance with national regulations (e.g., Health Insurance Portability and Accountability Act [HIPAA] authorization for United States [US] sites) prior to any study related procedures, including withdrawal of prohibited medications if applicable.
Read, understood, and provided written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization after the nature of the study has been fully explained and must be willing to comply with all study requirements and procedures.
Subject must have read, understood, and provided written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization after the nature of the study has been fully explained; and
Able to provide written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization
Ability to provide written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization
Patient will read, understand and sign the informed consent and Health Insurance Portability and Accountability Act (HIPAA) agreement
Able to provide informed consent and have signed an approved consent form that conforms to federal and institutional guidelines to ensure compliance with Health Insurance Portability and Accountability Act (HIPAA) regulations
Signed written informed consent including Health Insurance Portability and Accountability Act (HIPAA) according to institutional guidelines
Patients must have signed an approved informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization
Able and willing to sign an informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization
Subjects must sign a written informed consent and Health Insurance Portability and Accountability Act (HIPAA) consent prior to performance of study-specific procedures or assessments and must be willing to comply with treatment and follow-up
Signed written informed consent and Health Insurance Portability and Accountability Act (HIPAA) consent
Able and willing to sign an informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization
Subject must be fully informed about their illness and the investigational nature of the study protocol (including foreseeable risks and possible side effects) and must sign and date an Institutional Review Board-approved Informed Consent Form (including Health Insurance Portability and Accountability Act authorization, if applicable) before performance of any study specific procedures or tests.
Informed consent and Health Insurance Portability and Accountability Act (HIPAA) signing
Signed Health Insurance Portability and Accountability Act (HIPAA) compliant research authorization
Ability to provide written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization
The patient has provided written informed consent with Health Insurance Portability and Accountability Act (HIPAA) authorization before participating in the study, as has his/her responsible caregiver, if applicable
No history of hysterectomy; women will not be eligible for the pilot randomized controlled trial (RCT) if they participated in the focus groups that helped develop this study (focus groups were institutional review board [IRB] approved as Protocol C) or the preliminary device test; we will also require women to read and understand English and have the ability to provide informed consent, which will be inferred upon completion and return of the study eligibility, consent, and Health Insurance Portability and Accountability Act (HIPAA) forms
The patient has provided written informed consent with Health Insurance Portability and Accountability Act (HIPAA) authorization
All subjects, or their legal guardians, must sign a written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization in accordance with institutional guidelines
Participant will be fully informed and has personally signed and dated the written informed Consent and Health Insurance Portability and Accountability Act (HIPAA) provisions
All patients, or their legal guardians, must sign a written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization in accordance with institutional guidelines
All subjects, or their legal guardians, must sign a written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization in accordance with institutional guidelines
All subjects, or their legal guardians, must sign a written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization in accordance with institutional guidelines
All patients, or their legal guardians, must sign a written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization in accordance with institutional guidelines
All patients must sign a written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization in accordance with institutional guidelines
All patients, or their legal guardians, must sign a written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization in accordance with institutional guidelines
All patients must sign a written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization in accordance with institutional guidelines
Able to understand and willing to sign a written informed consent document and a Health Insurance Portability and Accountability Act (HIPAA) authorization in accordance with institutional guidelines
All participants, or their legal guardians, must sign a written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization in accordance with institutional guidelines
Patients must be able to provide written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization
Subjects, or their legal guardian, must sign a written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization in accordance with institutional guidelines
All patients must sign a written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization in accordance with institutional guidelines
Are fully informed about their illness and the investigational nature of the study protocol (including foreseeable risks and possible side effects) and must sign and date an Institutional Review Board (IRB)-approved informed consent form (ICF), including Health Insurance Portability and Accountability Act authorization, if applicable, before performance of any study-specific procedures or tests