HIV Clinical Trial
Official title:
Intervention Development for Newly Diagnosed Youth With HIV
| Verified date | August 2016 |
| Source | University of North Carolina, Chapel Hill |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
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.
| Status | Completed |
| Enrollment | 50 |
| Est. completion date | January 2009 |
| Est. primary completion date | June 2008 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 16 Years to 24 Years |
| Eligibility |
Inclusion Criteria: To be considered eligible for enrollment in ATN 068, a participant must meet the criteria listed below: - Receive services at one of the 4 selected ATN sites or their community partners; - HIV-infected as documented by medical record review or verbal verification with referring professional; - Received HIV diagnosis less than 15 months ago as documented by medical record review or verbal verification with referring professional; - Fall between the ages of 16-24 (inclusive) at the time of informed consent/assent; - Must be willing to participate in the both the individual and group sessions; - Give informed consent/assent for study participation. Exclusion Criteria: Participants who meet any of the exclusion criteria listed below are considered ineligible: - Acquired HIV through perinatal infection; - Presence of serious psychiatric symptoms (active hallucinations, thought disorder); - Visibly distraught (suicidal, homicidal, exhibiting violent behavior); - Intoxicated or under the influence of alcohol or other substances at the time of study enrollment. |
| Country | Name | City | State |
|---|---|---|---|
| United States | Montefiore Medical Center | Bronx | New York |
| United States | John Stroger Jr. Hospital of Cook County | Chicago | Illinois |
| United States | St. Jude Children's Research Hospital | Memphis | Tennessee |
| United States | University of Miami School of Medicine | Miami | Florida |
| Lead Sponsor | Collaborator |
|---|---|
| University of North Carolina, Chapel Hill | National Institute of Mental Health (NIMH), National Institute on Drug Abuse (NIDA) |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | The best procedures for a larger trial (e.g. timing, content etc. of ACASI administration) | 7 months | ||
| Primary | The appropriateness of specific instruments proposed. | 7 months | ||
| Primary | The perceived sensitivity of measures to change over time. | 7 months |
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