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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03899220
Other study ID # 2019p001118
Secondary ID K23DA043418
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date April 24, 2019
Est. completion date April 30, 2024

Study information

Verified date December 2023
Source Massachusetts General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will implement a pilot randomized controlled trial (RCT, N=60) to assess the feasibility and acceptability a refined emotion regulation intervention designed to improve engagement in HIV-care among substance using HIV+ MSM sub-optimally engaged in HIV care.


Description:

Eligible study participants will be screened and enrolled at Fenway Health (Boston, MA). Participants will be randomized to an enhanced treatment as usual (E-TAU) arm or the intervention arm. All participants (in both the E-TAU and intervention groups) will receive a one-session behavioral engagement in care intervention, substance use treatment referral information, and the opportunity to discuss and problem solve barriers to substance use treatment with an interventionist, informed by motivational interviewing principles. After randomization, participants in the intervention group will attend 5 therapy sessions focused on behavioral strategies for improving HIV self-care, meta-cognitive awareness of emotions and thoughts, and cognitive restructuring. All participants will receive texts queries about antiretroviral therapy (ART) adherence and substance use, and participants in the intervention group will also receive text queries about mood. All participants will be compensated for every research visit and completed text message blocks.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 50
Est. completion date April 30, 2024
Est. primary completion date May 30, 2023
Accepts healthy volunteers No
Gender Male
Age group 18 Years and older
Eligibility Inclusion Criteria: - HIV positive - Cisgender male - Man who has sex with men (MSM) - Elevated levels of internalized stigma related to HIV, substance use, or homophobia - Poorly engaged in HIV care - Able to provide informed consent - 18 years or older - English speaking Exclusion Criteria: - Women - Non-cisgender men - Do not identify as gay, bisexual, or MSM

Study Design


Intervention

Behavioral:
Project Matter
This intervention includes 5 face-to-face therapy sessions with a trained clinician plus a bidirectional text component that queries mood, substance use, and medication adherence. Both the intervention group and the enhanced treatment as usual (E-TAU) involve a one-session behavioral engagement in care intervention as well as substance use treatment counseling.

Locations

Country Name City State
United States Fenway Community Health Boston Massachusetts

Sponsors (2)

Lead Sponsor Collaborator
Massachusetts General Hospital National Institute on Drug Abuse (NIDA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Acceptability of Intervention The summary score of the Client Satisfaction Questionnaire (CSQ-8) (Sum of 8 questions with response options ranging from 1-4). change from baseline to 12 weeks after intervention completion
Primary Feasibility of Intervention Percent of sessions completed (=70% considered indicative of feasibility) and percent of text messages responded to by participants (=70% considered indicative of feasibility). change from baseline to 12 weeks after intervention completion
Secondary Engagement in HIV Care Summary Score of 6 indicators of HIV treatment engagement: no missed and not rescheduled HIV-related appointments in the past 3 months, no missed and not rescheduled HIV-related lab tests in the past 3 months, maintaining ART prescriptions over the past 3 months, maintaining >=80% ART adherence in the past 30 days, no period of 4 days where ART was stopped in the past 3 months (without guidance from an HIV care provider), and undetectable viral load at the study visit. change from baseline to 12 weeks after intervention completion
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