Project WERK (Wellness Encouragement Respect Kinship)

NCT ID: NCT03148171

Last Updated: 2024-05-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

290 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-10-09

Study Completion Date

2020-06-15

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The Project WERK intervention is a brief, theory based and culturally sensitive intervention designed to capitalize on organic yet underutilized social support networks in the lives of young black men who have sex with men (YBMSM). The intervention has been developed with input from clients and their support network members, case managers, social workers, primary care providers. The goal of the intervention is to improve retention in PrEP care for young Black MSM.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Project WERK will recruit, consent and randomize 160 men, with 80 men randomized to each arm of the study. Men randomized to the control condition will receive standard PrEP care at each clinical site. Men randomized to the experimental condition will receive standard PrEP care and also will be asked to recruit a supportive contact from their social network. The support contact will then be engaged in a brief intervention designed to support their friend/family member around PrEP Care. Men and support contacts in the WERK intervention also will receive booster sessions via telephone and text. All participants will complete surveys at baseline and at three and twelve months post intervention.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

HIV Prevention

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Routine PrEP Care

Routine PrEP Care at each clinical site.

Group Type NO_INTERVENTION

No interventions assigned to this group

WERK Supportive Contact

Support contact will provide emotional support and practical support in order to help their friend/family member to stay engaged in PrEP Care.

Group Type ACTIVE_COMPARATOR

WERK Supportive Contact

Intervention Type OTHER

Provide emotional support and practical support. Support friend/family by helping him to stay engaged in PrEP Care.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

WERK Supportive Contact

Provide emotional support and practical support. Support friend/family by helping him to stay engaged in PrEP Care.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

Index subjects:

* Self-identify as African American/Black;
* Assigned male sex at birth;
* Any same gender anal or oral sex in the past 2 years;
* English speaking;
* Have at least one support contact in their network;
* Own a cell phone not shared with other persons;
* Between the ages of 18-35 years old; and
* Have had fewer than 3 PrEP clinical visits in the past 12 months.

Support Contact:

* Index participant has agreed to including the support contact
* Willing to attend face to face and telephone mini-booster sessions;
* 18 years of age or older;
* English speaking; and
* Owns a cell phone that is not shared with other persons.

Exclusion Criteria

Index Subject:

* Unable to provide informed consent;
* Plan to move out of the area within the next 12 months;
* Are not willing to attend intervention sessions; or
* Not willing to return for assessments.

For index participants without a support contact, we will refer them to an appropriate support group for PrEP.

Support Contact:

* Romantic partner of index participant;
* Unable to provide informed consent;
* Plan to move out of the area within the next 12 months;
* Are not willing to attend intervention sessions; or
* Not willing to return for assessments.
Minimum Eligible Age

18 Years

Maximum Eligible Age

35 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Howard Brown Health Center

OTHER

Sponsor Role collaborator

Ann & Robert H Lurie Children's Hospital of Chicago

OTHER

Sponsor Role collaborator

National Institute of Mental Health (NIMH)

NIH

Sponsor Role collaborator

University of Chicago

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Alida Bouris, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Chicago

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Chicago Center for HIV Elimination

Chicago, Illinois, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

R34MH111392

Identifier Type: NIH

Identifier Source: secondary_id

View Link

IRB17-0152

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

The Collaborative Care PrTNER Study
NCT06585631 RECRUITING NA