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NCT02411630 · ClinicalTrials.gov registry record

Factors Affecting PrEP Adherence

A clinical trial, sponsored by University of North Carolina, Chapel Hill.

Completed
Registry status
167
Enrollment target

NCT02411630: Completed study, sponsored by University of North Carolina, Chapel Hill.

NCT02411630 is a clinical trial that has completed, run by University of North Carolina, Chapel Hill. The registered enrollment target is 167 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02411630 has completed, sponsored by University of North Carolina, Chapel Hill.

COMPLETED
Registry status
167 participants
Enrollment target

Study Summary

The purpose of this study is to test a new way to take a questionnaire that asks about adherence (whether the person is taking the medicine correctly). This new questionnaire is called Interactive Questionnaire System (iQS). In this study, the iQS will be tested on HIV-negative young men who have sex with men (YMSM) who are taking PrEP as part of another study, either ATN 110 or ATN 113.

Primary Outcome

To assess preference of the iQS as a way to measure adherence to Pre-Exposure Prophylaxis (PrEP) in PrEP clinical trials, completion rates; pattern of skipped or incomplete responses by variables will be analyzed.

Interventions

  • DRUG Emtricitabine/tenofovir disoproxil

Trial Details

FieldValue
Enrollment Target 167 participants
Start Date 2013-06
Est. Completion 2015-06

What the finished NCT02411630 record still lists

NCT02411630 is an observational study that tracks outcomes without assigning an intervention. The registered 167 participants enrollment target is mid-sized for trials with a published cap.

The record links to 0 conditions, and to 1 intervention - of which Emtricitabine/tenofovir disoproxil is the first listed.

NCT02411630 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02411630 about?

NCT02411630 is a clinical study titled "Factors Affecting PrEP Adherence". The purpose of this study is to test a new way to take a questionnaire that asks about adherence (whether the person is taking the medicine correctly). This new questionnaire is called Interactive Questionnaire System (iQS). In this study, the iQS will be tested on HIV-negative young men who have se...

What is the current status of trial NCT02411630?

This trial is currently completed. The enrollment target is 167 participants. The study started on 2013-06. Estimated completion is 2015-06.

What interventions are being tested in trial NCT02411630?

The interventions under investigation include: Emtricitabine/tenofovir disoproxil (DRUG).

Who is sponsoring clinical trial NCT02411630?

This trial is sponsored by University of North Carolina, Chapel Hill, which has 1,109 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT02411630, the US trial registry maintained by the National Library of Medicine. NCT02411630 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.