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Trial · NCT07900750

Registered outcomes11

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryTime to ART re-initiation (Stage 1)From initial randomization through end of study follow-up, up to 12 monthsTime to confirmed receipt of ART during a return clinic visit or community-based medication delivery by a navigator
PrimaryTime to Repeat Treatment Interruption after Return (Stage 2)From Return to Care and Second Stage Randomization to 12 months laterTime to missing a pharmacy refill by \>14 days after return
PrimaryProportion of Time Spent in Care and with medications (Stage 1 + Stage 2)From Treatment Interruption until 18-monthsDays spent in care and not \>14 days late for ART pick-up
SecondaryViral Suppression12-18 months
Percentage of participants with documented viral suppression, defined as HIV RNA \<400 copies/mL, compared across the six embedded sequential return-and-reengagement strategies. Viral load data are drawn from the national electronic health record (SmartCare), supplemented by field-based viral load collection where necessary.
SecondaryPercentage of Participants Engaged in Care 12 to 18 Months After Initial Randomization12 to 18 months after initial treatment interruption
SecondaryTime to return for a clinic visitFrom initial treatment interruption through end of study follow-up, up to 12 monthsTime from initial randomization to first completed HIV clinic visit
SecondaryProportion who return to clinic within 3-monthsAt 3-months initial treatment interruption
SecondaryProportion successfully contacted via phone or in-personAt 3-months initial treatment interruption
SecondaryPercent with at least one pharmacy refill missed by >30 daysFrom second-stage re-randomization up to 12 months
SecondaryPercentage of Participants Attending Any Clinic Visit 6 to 12 Months After Return to Care6 to 12 months after return to care
SecondaryCost Effectiveness12 monthsAssessing the cost-effectiveness of return strategies (Aim 1a), reengage strategies (Aim 1b), and sequential combination return-and-reengage strategies (Aim 2).

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this list from software.

Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT07900750/registered