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NCT07192419

Promoting Aging and Thriving With HIV

Enrolling by Invitation
NAAges 50+InterventionalScreening
Indiana University
~60 participants
Updated 2025-12-19 on ClinicalTrials.gov
What's tested:Promoting Aging and Thriving with HIV (PATH)-Implementation of a Tailored Geriatric Assessment and Management Strategy for HIV Care Settings

At a glance

Recruiting sites
0 of 2 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Feasibility: recruitment and retention
Measured over Recruitment day one, throughout the study to final assessment six months post baseline of the last participant.
+2 more outcomes measured

Conditions

HIV (Human Immunodeficiency Virus)
Geriatric
Geriatric Assessment
HIV
HIV - Human Immunodeficiency Virus

Explore related trials

HIV Infection

Where it's being run

2 sites across 1 states
Indiana2

Study leadership

  • Meredith Greene, MD · PRINCIPAL_INVESTIGATOR · Indiana University School of Medicine, and Regenstrief Institute; IU Center for Aging Research

Who to contact

This trial hasn't published a contact. View it on ClinicalTrials.gov

Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

Age 50 or older
Receive HIV care (at least 1 visit at the same site within the past 12 months) from either Eskenazi Health IDC or LifeCare clinics,
Able to provide informed consent

Exclusion

Patients who are long-term nursing home residents
Patients who are receiving geriatric care services, however will liberalize this criteria if difficulty with recruitment

What this trial measures

  • Feasibility: recruitment and retentionRecruitment day one, throughout the study to final assessment six months post baseline of the last participant.

    Feasibility will be measured by tracking the number of participants approached, enrolled, retained, observations by study team throughout study.

  • Feasibility: patient/provider experienceAfter completing final outcomes at the 6 month assessment (or earlier if difficulty with recruitment/retention) patients and providers will be invited to participate in an optional qualitative interview.

    Feasibility will be measured by qualitative Interviews with patients and providers. Interview questions will be used to derive personal anecdotes of the patient/provider experience pertaining to the feasibility of the study.

  • Acceptability; General attitudes, perception of interventionAfter completing final outcomes at the 6 month assessment (or as needed if difficulty with recruitment/retention) patients and providers will be invited to participate in an optional qualitative interview.

    Acceptability will be measured by qualitative Interviews with patients and providers. Interview questions will be used to derive personal anecdotes of the patient/provider general attitudes, perception of intervention.