search
Back to results

Evaluating the Efficacy of Annual CHTC Retesting Among Male Couples at High Risk of HIV Infection (4Us Part B)

Primary Purpose

HIV Infections

Status
Enrolling by invitation
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Couples HIV testing and counseling
Individual HIV testing and counseling
Sponsored by
Hunter College of City University of New York
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for HIV Infections

Eligibility Criteria

17 Years - 65 Years (Child, Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion: enrolled previously in the parent study DA050508 (NCT05000866). in a relationship with the same main partner with whom they completed the baseline intervention session. both partners in the couple must consent to continue with activities specified in this revision. completion of the 12-month assessment associated with participation in the parent study prior to consenting to participate in activities specified under this revision. Exclusion: any of the following at the 12-month follow-up: serious psychiatric symptoms; current suicidal/homicidal ideation; gross cognitive impairment a history of severe physical or sexual Intimate Partner Violence (IPV) victimization in the current relationship.

Sites / Locations

  • University of Michigan
  • Hunter College

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Couples HIV testing and counseling retesting

Individual HIV testing

Arm Description

Couples HIV testing and counseling is completed following Centers for Disease Control and Prevention (CDC) standard protocol. Participants also complete any adjunct CHTC components associated with their originally assigned condition in NCT05000866.

Individual HIV testing and counseling.

Outcomes

Primary Outcome Measures

number of condomless anal sex acts with a casual partner in the absence of PrEP
Number of total anal sex acts (insertive and receptive) with casual partners reported on quarterly timeline follow-back assessments

Secondary Outcome Measures

Binge drinking
Number of days on which 5 or more drinks containing alcohol were reported on the quarterly timeline follow-back interview
pre-exposure prophylaxis (PrEP) uptake
self-reported receipt of a PrEP-prescription
PrEP adherence
taking 4 or more doses weekly as prescribed reported on quarterly timeline follow-back assessments
Drug use Frequency
Number of reported days of illicit drug use (amphetamines, cocaine/crack, gama hydroxybutyric acid (GHB), ketamine or ecstasy) reported on quarterly timeline follow-back assessments

Full Information

First Posted
April 17, 2023
Last Updated
May 10, 2023
Sponsor
Hunter College of City University of New York
Collaborators
National Institute on Drug Abuse (NIDA), University of Michigan
search

1. Study Identification

Unique Protocol Identification Number
NCT05833074
Brief Title
Evaluating the Efficacy of Annual CHTC Retesting Among Male Couples at High Risk of HIV Infection
Acronym
4Us Part B
Official Title
Evaluating the Efficacy of Annual CHTC Retesting Among Male Couples at High Risk of HIV Infection
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Enrolling by invitation
Study Start Date
April 1, 2023 (Actual)
Primary Completion Date
May 31, 2025 (Anticipated)
Study Completion Date
May 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hunter College of City University of New York
Collaborators
National Institute on Drug Abuse (NIDA), University of Michigan

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This randomized controlled trial evaluates the efficacy of couples HIV testing and counseling retesting. Eligible couples previously enrolled in NCT05000866 are invited to participate. Those who do are randomized to either couples HIV testing and counseling (CHTC) retesting or an individual HIV testing control. Follow-ups occur 3 and 6 months post intervention.
Detailed Description
The purpose of this study is to evaluate the benefits associated with couples HIV testing and counseling (CHTC) resting. After their 12-month follow-up, those participants who remain in the same relationship they were in at the time of their baseline will be offered the opportunity to continue in the components proposed in this revision. Those who consent will be randomized to either complete a second session of CHTC or to a comparison condition in which both partners receive a routine individual HIV test. HIV positive partners in serodiscordant couples randomized to the control condition will receive information about anti-retroviral treatment adherence and U=U (undetectable = untransmissible). Given potential attrition and rates of relationship dissolution, we anticipate randomizing 200 couples (80% of the original sample). Follow-up assessments will be conducted 3 and 6 months after retesting (15 and 18 months after the participants' original baseline appointment).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants are randomized (with equal allocation) to either couples HIV testing and counseling retesting or an individual HIV testing control.
Masking
Outcomes Assessor
Masking Description
Research assistants are not given access to information about study condition.
Allocation
Randomized
Enrollment
384 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Couples HIV testing and counseling retesting
Arm Type
Experimental
Arm Description
Couples HIV testing and counseling is completed following Centers for Disease Control and Prevention (CDC) standard protocol. Participants also complete any adjunct CHTC components associated with their originally assigned condition in NCT05000866.
Arm Title
Individual HIV testing
Arm Type
Active Comparator
Arm Description
Individual HIV testing and counseling.
Intervention Type
Behavioral
Intervention Name(s)
Couples HIV testing and counseling
Other Intervention Name(s)
CHTC
Intervention Description
Couples HIV testing follows a CDC published protocol for delivery of HIV testing to relationship partners. HIV test results are obtained from Oraquick (FDA approved for at home HIV testing)
Intervention Type
Behavioral
Intervention Name(s)
Individual HIV testing and counseling
Other Intervention Name(s)
HTC
Intervention Description
Individual HIV testing and counseling uses a counseling protocol based on the standard of care for routine HIV pre- and post-test counseling. HIV test results are obtained from Oraquick (FDA approved for at home testing)
Primary Outcome Measure Information:
Title
number of condomless anal sex acts with a casual partner in the absence of PrEP
Description
Number of total anal sex acts (insertive and receptive) with casual partners reported on quarterly timeline follow-back assessments
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Binge drinking
Description
Number of days on which 5 or more drinks containing alcohol were reported on the quarterly timeline follow-back interview
Time Frame
6 months
Title
pre-exposure prophylaxis (PrEP) uptake
Description
self-reported receipt of a PrEP-prescription
Time Frame
6 months
Title
PrEP adherence
Description
taking 4 or more doses weekly as prescribed reported on quarterly timeline follow-back assessments
Time Frame
6 months
Title
Drug use Frequency
Description
Number of reported days of illicit drug use (amphetamines, cocaine/crack, gama hydroxybutyric acid (GHB), ketamine or ecstasy) reported on quarterly timeline follow-back assessments
Time Frame
6 months

10. Eligibility

Sex
Male
Gender Based
Yes
Gender Eligibility Description
cismale
Minimum Age & Unit of Time
17 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion: enrolled previously in the parent study DA050508 (NCT05000866). in a relationship with the same main partner with whom they completed the baseline intervention session. both partners in the couple must consent to continue with activities specified in this revision. completion of the 12-month assessment associated with participation in the parent study prior to consenting to participate in activities specified under this revision. Exclusion: any of the following at the 12-month follow-up: serious psychiatric symptoms; current suicidal/homicidal ideation; gross cognitive impairment a history of severe physical or sexual Intimate Partner Violence (IPV) victimization in the current relationship.
Facility Information:
Facility Name
University of Michigan
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States
Facility Name
Hunter College
City
New York
State/Province
New York
ZIP/Postal Code
10018
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Participant-level data will be shared upon request and at the discretion of the study PI under the terms of a memorandum of understanding signed by officials at the transmitting and receiving institutions.

Learn more about this trial

Evaluating the Efficacy of Annual CHTC Retesting Among Male Couples at High Risk of HIV Infection

We'll reach out to this number within 24 hrs