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NCT05912374 · ClinicalTrials.gov registry record · NA

Adapting a Behavioral Intervention to Accommodate Cognitive Dysfunction in People Who Inject Drugs

A NA study, sponsored by University of Connecticut.

Completed
Registry status
NA
Development phase
50
Enrollment target

NCT05912374 is a NA study that has completed, run by University of Connecticut. The registered enrollment target is 50 participants.

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The verdict

NCT05912374, a NA study, has completed, sponsored by University of Connecticut.

COMPLETED
Registry status
NA
Development phase
50 participants
Enrollment target

Study Summary

The goal of this pilot work was to determine if the cognitive dysfunction accommodation strategies help patients retain/utilize more HIV prevention information and increase PrEP adherence. Fifty people who inject drugs (PWID) were prescribed PrEP and randomized to one of two conditions, Twenty-five PWID participated in a standard HIV prevention session and 25 other PWID participated in a HIV prevention session with the included accommodation strategies. At recruitment participants were asked to provide self-report of the screening form and cognitive functioning. The intervention consisted of a total of 5 sessions: 1 meeting to gain baseline information of participants and 4 intervention sessions. Participants completed the consent form, demographics, skills assessment, drug use behavior assessment, and HIV risk behavior assessment at the pre-interview meeting. Participants completed PrEP uptake assessments and skills assessments immediately following the intervention to compare the pre/post results between the two groups. All participants also completed an acceptability rating to help researchers determine the acceptability of the accommodation strategies used, at the end of the 4th session. The objective was to determine if the proposed accommodation strategies are feasible and efficacious at improving HIV prevention outcomes, including knowledge and skills. Information gleaned from this process will be used to refine the intervention approach for future testing and implementation.

Interventions

  • BEHAVIORAL standard Community-Friendly Health Recovery Program- Biobehavioral (CHRP-BB)
  • BEHAVIORAL enhanced Community-Friendly Health Recovery Program- Biobehavioral (CHRP-BB)

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2022-09-07
Est. Completion 2022-12-12
Phase NA

Sponsor

University of Connecticut

107 total trials

What the Registry Record Tells You About NCT05912374

The ClinicalTrials.gov registry entry for NCT05912374 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Connecticut, which has 107 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which standard Community-Friendly Health Recovery Program- Biobehavioral (CHRP-BB) is the first listed.

NCT05912374 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT05912374 about?

NCT05912374 is a clinical study titled "Adapting a Behavioral Intervention to Accommodate Cognitive Dysfunction in People Who Inject Drugs". The goal of this pilot work was to determine if the cognitive dysfunction accommodation strategies help patients retain/utilize more HIV prevention information and increase PrEP adherence. Fifty people who inject drugs (PWID) were prescribed PrEP and randomized to one of two conditions, Twenty-five ...

What is the current status of trial NCT05912374?

This trial is currently completed. It is a NA study. The enrollment target is 50 participants. The study started on 2022-09-07. Estimated completion is 2022-12-12.

What interventions are being tested in trial NCT05912374?

The interventions under investigation include: standard Community-Friendly Health Recovery Program- Biobehavioral (CHRP-BB) (BEHAVIORAL), enhanced Community-Friendly Health Recovery Program- Biobehavioral (CHRP-BB) (BEHAVIORAL).

Who is sponsoring clinical trial NCT05912374?

This trial is sponsored by University of Connecticut, which has 107 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.