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NCT05708014 · ClinicalTrials.gov registry record · NA

Personalized Prevention for Couples: A 16-month Digital RCT

A NA study, sponsored by Florida International University.

Completed
Registry status
NA
Development phase
778
Enrollment target

NCT05708014: Completed NA study, sponsored by Florida International University.

NCT05708014 is a NA study that has completed, run by Florida International University. The registered enrollment target is 778 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (45% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05708014, a NA study, has completed, sponsored by Florida International University.

COMPLETED
Registry status
NA
Development phase
778 participants
Enrollment target

Study Summary

This couples-based, digital health intervention project is serostatus neutral and seeks to determine efficacy for: a) use and adherence to evidence-based HIV/STI prevention-care strategies; b) creation and adherence to a tailored prevention-care plan; c) creation and adherence to a tailored sexual agreement; and d) improvements in other relationship dynamics among male couples who are in a relationship (defined as greater than 3 months or more).

Primary Outcome

Participants will be asked to provide sample to test for HIV at baseline and 16-months, using at-home self-collection test kits. Count: New HIV and STI diagnosis via biomedical testing at follow-up occurring 16 months after baseline randomization.

Interventions

  • BEHAVIORAL Intervention LuvHub
  • BEHAVIORAL Waitlist Control LuvHub

Trial Details

FieldValue
Enrollment Target 778 participants
Start Date 2023-01-11
Est. Completion 2025-08-25
Phase NA
Florida International University

89 total trials

What the finished NCT05708014 record still lists

NCT05708014 is an interventional study that assigns participants to a tested intervention. The registered 778 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (45% lower).

The record links to 0 conditions, and to 2 interventions - of which Intervention LuvHub is the first listed.

NCT05708014 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05708014 about?

NCT05708014 is a clinical study titled "Personalized Prevention for Couples: A 16-month Digital RCT". This couples-based, digital health intervention project is serostatus neutral and seeks to determine efficacy for: a) use and adherence to evidence-based HIV/STI prevention-care strategies; b) creation and adherence to a tailored prevention-care plan; c) creation and adherence to a tailored sexual a...

What is the current status of trial NCT05708014?

This trial is currently completed. It is a NA study. The enrollment target is 778 participants. The study started on 2023-01-11. Estimated completion is 2025-08-25.

What interventions are being tested in trial NCT05708014?

The interventions under investigation include: Intervention LuvHub (BEHAVIORAL), Waitlist Control LuvHub (BEHAVIORAL).

Who is sponsoring clinical trial NCT05708014?

This trial is sponsored by Florida International University, which has 89 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05708014's enrollment target sits among peer trials

778 142nd of 2000 higher than 1,859 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05708014, the US trial registry maintained by the National Library of Medicine. NCT05708014 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.