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