Clinical Research Directory

Inclusion Criteria: * Adults aged 18 years or older. * Able and willing to provide informed consent, when informed consent is required by the approved study protocol and applicable regulations. * Willing and able to participate in longitudinal collection or evaluation of clinical, physiologic, laboratory, imaging-derived, patient-reported, or remote/digital health information as applicable to the study protocol. * Ability to complete the protocol-defined follow-up schedule or provide sufficient longitudinal observations for analysis. * Individuals with or without established medical conditions may be eligible, provided their participation is consistent with the study protocol. * Availability of sufficient baseline information or measurements to establish an individualized reference state when required for the applicable analysis. Exclusion Criteria: * Inability to provide informed consent when consent is required and no legally authorized representative process is applicable. * Inability to comply with protocol-defined data collection or follow-up requirements. * Circumstances that, in the judgment of the investigator, would prevent reliable longitudinal data collection or interpretation. * Enrollment in another research protocol that would materially interfere with participation or interpretation of the outcomes, when applicable. * Any other exclusion criterion specifically identified in the IRB/ethics-approved protocol.