Care Disengagement Prevention in PLWH in Indonesia (NCT07706634) | Clinical Trial Compass
RecruitingNot Applicable
Care Disengagement Prevention in PLWH in Indonesia
Indonesia110 participantsStarted 2026-02-11
Plain-language summary
This study is being done because the investigators want to learn about how stigma and culture in Indonesia affects how much contact people living with HIV have with the healthcare system and also how it might affect their health status.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Living with HIV
* Able to give informed consent
* Able to attend study visits
Exclusion Criteria:
* Condition that prevents full participation in the study such as neurological disease, major depression or cardiovascular disease
* Unable to communicate
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Change in Perceived Stigma Score From Baseline to End of Intervention
Timeframe: Baseline to 26 weeks
2
Change in Adherence From Baseline to End of Intervention
Timeframe: Baseline to 26 weeks
3
Level of Healthcare Engagement From Baseline to End of Intervention as Measured by Missed or Delayed Clinic Visits
Timeframe: Baseline to 26 weeks
4
Changes in Patient Activation from Baseline to End of Intervention
Timeframe: Baseline to 26 weeks
5
Change in Internal Stigma Score From Baseline to End of Intervention