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| Name | Class |
|---|---|
| National Institute on Drug Abuse (NIDA) | NIH |
| National Institute of Mental Health (NIMH) | NIH |
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This study will pilot test an HIV intervention for newly diagnosed youth (diagnosed for less than 15 months) to assess its acceptability and feasibility preliminary to and leading up to a full-scale, randomized trial. The general focus of the intervention is to aid in the psychosocial adjustment of adolescents who have recently been diagnosed with HIV.
The intervention will consist of a combination of individual and group-based sessions in which the youth will participate. This combination allows for more intensive individualized attention as well as supportive group sessions. Youth will first participate in two individual sessions, followed by nine group sessions, and end with one additional individual session.
Individual Session I: Orientation I
Part A - meet with interventionist for ecological assessment, rapport building, and preparation for meeting with medical provider Part B - meet with medical provider to answer HIV specific medical questions (i.e., transmission information, viral load/t-cells, opportunistic infections,etc.). The interventionist will be present in Part B as well.
Individual Session II: Orientation II
Part A - meet with interventionist for continued debriefing, question/answer, preparation for group participation.
Part B - meet with peer facilitator to discuss individual experiences living with HIV, rapport building, peer-specific questions. The interventionist will be present in Part B as well.
Individual session III: Wrap-up and Action Planning (to take place after group sessions are complete)
Part A - action plan with linkage to identified agencies via facilitated referrals Part B - (optional) support building - participants may bring parents, partner, friend, or other potential source of support for question/answer session with interventionist
Session I: Developing Group Cohesion
- Icebreaker, team building, group rules, facilitation of group "ownership" by participants.
Session II: Disclosure, Stigma & Relationships
Session III: Preparing for Medical Intervention
- Working with medical providers, an overview of clinic appointments and expectations surrounding attendance, a preliminary discussion of medications, side effects, and medical management as well as strategies for adherence.
Session IV: Healthy Living
Session V: Stress Reduction/Relaxation & Spirituality
Session VI: Gender Specific
Session VII: Self-Esteem/Self-Worth
- Strategies to improve self-esteem and self-worth;
Session VIII: Legal Issues/Advocacy
Session IX: Future Planning
- Planning for the future including issues related to work and school (e.g., job application process, applying for financial aid), job training and career choices.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 1 | Experimental | 5-7 females per group at each of the four sites. |
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| 2 | Experimental | 5-7 males per group at each of the four sites. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| "Adolescents Coping, Connecting, Empowering, and Protecting Together" (Project ACCEPT) | Behavioral | The intervention will consist of a combination of individual and group-based sessions in which the youth will participate. This combination allows for more intensive individualized attention as well as supportive group sessions. Youth will first participate in two individual sessions, followed by nine group sessions, and end with one additional individual session. |
| Measure | Description | Time Frame |
|---|---|---|
| The best procedures for a larger trial (e.g. timing, content etc. of ACASI administration) | 7 months | |
| The appropriateness of specific instruments proposed. | 7 months | |
| The perceived sensitivity of measures to change over time. | 7 months |
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Inclusion Criteria:
To be considered eligible for enrollment in ATN 068, a participant must meet the criteria listed below:
Exclusion Criteria:
Participants who meet any of the exclusion criteria listed below are considered ineligible:
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| Name | Affiliation | Role |
|---|---|---|
| Sybil Hosek, PhD | John Stroger Jr. Hospital of Cook County | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Miami School of Medicine | Miami | Florida | 33101 | United States | ||
| John Stroger Jr. Hospital of Cook County |
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| Label | URL |
|---|---|
| Website for the Adolescents Trials Network for HIV/AIDS Interventions | View source |
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|
| Chicago |
| Illinois |
| 60612 |
| United States |
| Montefiore Medical Center | The Bronx | New York | 10467 | United States |
| St. Jude Children's Research Hospital | Memphis | Tennessee | 38105 | United States |