Examining the Health Effects of NPOWER365 Among Black Same Gender Loving Men

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorRutgers, The State University of New Jersey

About this trial

This research study aims to test the effectiveness, reach, and maintenance over time of the NPOWER365 HIV care intervention for Black men who have sex with men (BMSM) living with HIV. NPOWER365 is a BMSM community-developed multicomponent intervention that aims to: 1) Support daily health promotion via HIV health education and health maintenance reminders; 2) Foster positive social connections among BMSM via online moderated forums, interpersonal chats, and community calendars; 3) Connect clients to BMSM-affirming healthcare, including HIV treatment and mental healthcare; 4) Provide resources for housing, transportation, and other economic empowerment.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Identify as Black or African American, regardless of ethnicity

Identify as male, regardless of sex assigned at birth

Are living with HIV and prescribed a daily ART regimen

Are age ≥ 18;

Disqualifiers

Lack of English fluency

Past participation in the pilot.

Trial design

Design model

Parallel

Treatments tested in this trial

  • NPOWER365 HIV care intervention

    Behavioral

    NPOWER365 is a multicomponent intervention that combines mHealth features and institutional to support community priorities identified in formative CBPR. In line with best-practices for trials of intervention principles (TIPs) with mHealth interventions, NPOWER365 deploys intervention elements that serve to accomplish intervention strategies. NPOWER365 intervention strategies are to promote: 1)Health knowledge and motivation; 2)Social support coping; 3)Access to culturally-affirming healthcare; and 4)Housing and other economic resources. NPOWER365 pursues these strategies via these intervention elements: 1)Weekly HIV and psychological health information and motivation content and daily health notifications; 2)Online moderated forums, interpersonal chats, and community calendars; 3)Linkage to biopsychosocial healthcare via NAESM's network of Black SGLM-affirming providers; and 4)Housing and economic resources through NAESM's direct support and referral network.

Treatment groups

350 Participants
are divided into 2 treatment groups
Group A: Intervention ArmExperimental treatment 1 intervention
Group B: Control ArmNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Antiretroviral (ART) Medication Use

For daily surveys, participants will report ART adherence on a single binary item ("In the past 24 hours did the participant take ART medication?")

Time frame
24 hours
2

ART adherence-Long Lag Assessments

The investigators will use the NAME scale that assesses barriers to ART adherence.

Time frame
2 weeks

Secondary outcomes

1

Daily Diary Substance Use

The investigators will measure daily substance use with single-item binary measures of various substances (e.g.,alcohol, marijuana).

Time frame
24 hours
2

Substance Use-Long Lag Assessments

For long lags (i.e., 2 week assessment to 6 month assessment), participants will complete an online, automated retrospective assessment of substance use in the past 2 weeks.

Time frame
2 weeks
3

Depressive Symptoms

The Patient Health Questionnaire-4 assesses anxiety and depressive symptoms. Participants rate the extent to which the participants had been experiencing each item the past day (e.g., "In the past 24 hours, I've been feeling nervous, anxious, or on edge") on a scale from 0 (not at all) to 3 (entirely). The investigators used an average across all items for each time point.

Time frame
24 hours
4

Depressive Symptoms-Long Lag

The Brief Symptom Inventory assesses anxiety and depressive symptoms. Participants rate the extent to which the participants had been experiencing each item the past two weeks (e.g., "Feeling hopeless about the future") on a scale from 0 (not at all) to 4 (Extremely). The investigators will use an average across all items for each time point.

Time frame
2 weeks

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Rutgers, The State University of New Jersey

Lead sponsor

Positive Impact Health Centers

Collaborator

George Washington University

Collaborator

Carnegie Mellon University

Collaborator

Emory University

Collaborator

Columbia University

Collaborator

Arizona State University

Collaborator

NAESM, Inc.

Collaborator

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