Project ACCEPT: Engaging Newly Diagnosed HIV+ Youth in Care

NCT01751620 | Completed

• 1 other identifier: ATN 108
• Study Type: interventional
• Target: 167
• Locations: 1 country
• Sites: 4

Brief Summary

The proposed study is a two-group randomized repeated measures design that will examine the efficacy of Project ACCEPT (Adolescents Coping, Connecting, Empowering and Protecting Together) to improve engagement in care among youth newly diagnosed with HIV at five AMTU sites across the United States. Youth will be randomized into one of two study arms; Project ACCEPT, the intervention, or HEALTH, the health education attention-controlled comparison condition. Both arms consist of two individual sessions followed by six group sessions and a final individual session which is expected to take approximately nine weeks after which youth will have four follow-up visits at the following time points:

• post intervention (immediately after the last session);
• 3 months post the last session;
• 6 months post the last session; and
• 12 months post the last session. The trial will be repeated in up to three waves.

Conditions

HIV Positive Youth That Are Newly Engaged in Care

Outcome Measures

Primary Outcomes (1)

• Examine the efficacy of Project ACCEPT compared with an attention-controlled health education comparison intervention

  Conduct a randomized controlled trial to examine the efficacy of Project ACCEPT compared with an attention-controlled health education comparison intervention (HEALTH). The goals of the intervention are to improve engagement in care, decrease psychosocial barriers to care, and decrease sexual risk for youth newly diagnosed with HIV.

  3 years

Secondary Outcomes (1)

• Explore the relationship between HIV biomarkers and participant's level of engagement in care

  3 years

Study Arms (2)

Project ACCEPT

EXPERIMENTAL

Participants randomized to the intervention (Project ACCEPT) arm.

Behavioral: Project ACCEPT

HEALTH

ACTIVE COMPARATOR

Participants randomized to the comparison (HEALTH) arm.

Behavioral: HEALTH

Interventions

Project ACCEPT BEHAVIORAL

The intervention, Project ACCEPT, combines weekly individual and group sessions that address a range of issues that impact engagement in care for youth living with HIV, including stigma, disclosure, health relationships, substance use, and future life plans.

Also known as: Adolescents Coping, Connecting, Empowering and Protecting Together

Project ACCEPT

HEALTH BEHAVIORAL

The comparison condition, HEALTH, matches Project ACCEPT in number of sessions and duration. The weekly sessions will cover information on alcohol, drugs, HIV and other sexually transmitted diseases (STDs) to meet the ethical responsibility to provide risk reduction information to youth assigned.

HEALTH

Eligibility Criteria

• Age: 16 Years - 24 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Child (0-17), Adult (18-64)

You may qualify if:

• HIV-infected and aware of his/her status as documented by medical record review or verbal verification by provider (i.e., medical or mental health care provider, case manager, social worker, etc.);
• Received HIV diagnosis within the past 12 months (+ 3 months) at the time of consent/assent as documented by medical record review or verbal verification with referring professional (i.e., medical or mental health care provider, case manager, social worker, etc.);
• Between the ages of 16-24 (inclusive) at the time of informed consent/assent;
• Receives services at one of the selected AMTUs or one of their community partners;
• Willing to participate in both the individual and group sessions;
• Ability to speak and understand spoken English;
• Able to understand and willing to provide signed informed consent/assent in English or Spanish; and
• Willingness to provide signed informed consent or assent with parental/legal guardian permission as applicable.

You may not qualify if:

• Participated in a previous wave, if enrolling into Wave 2 or 3;
• Intoxicated or under the influence of alcohol or other substances at the time of consent/assent;
• Visibly distraught and/or visibly emotionally unstable (i.e., exhibiting suicidal, homicidal, or violent behavior) in the opinion of the site personnel would interfere with the ability to give true informed consent; and
• Any concurrent participation in other behavioral studies. Permission from the protocol team may be provided for uncertain cases.

Sponsors & Collaborators

• University of North Carolina, Chapel Hill: lead
• National Institute on Drug Abuse (NIDA): collaborator
• National Institute of Mental Health (NIMH): collaborator

Study Sites (4)

University of Miami School of Medicine

Miami, Florida, 33101, United States

Location

Stroger Hospital and the CORE Center

Chicago, Illinois, 60612, United States

Location

Wayne State University

Detroit, Michigan, 48201, United States

Location

St. Jude Childrens Research Hospital

Memphis, Tennessee, 38105, United States

Location

Related Links

• ATN website

MeSH Terms

Interventions

Health

Intervention Hierarchy (Ancestors)

Population Characteristics

Study Officials

• Sybil Hosek, PhD

  Adolescent Trials Network

  STUDY CHAIR

• Gary Harper, PhD

  Adolescent Trials Network

  STUDY CHAIR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: SUPPORTIVE CARE
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: December 14, 2012
• First Posted: December 18, 2012
• Study Start: January 1, 2013
• Primary Completion: June 1, 2015
• Study Completion: June 1, 2015
• Last Updated: February 28, 2017

Record last verified: 2016-10

Locations

US (4)