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Healthy Choices to Promote Health and Reduce Risk in HIV-Infected Youth

Primary Purpose

HIV Infection

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Healthy Choices - Motivational Enhancement Intervention
Standard care
Sponsored by
University of North Carolina, Chapel Hill
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV Infection focused on measuring motivational enhancement, health behaviors, risk behaviors

Eligibility Criteria

16 Years - 24 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: HIV infection as documented by professional referral and medical record review. HIV+ participants who are self-referred and not in medical care will be required to provide documentation of test results. Males or females between the age of 16 years and 0 days and 24 years and 364 days at the time of study enrollment. Reports having ever engaged in at least 2 of the following 3 behaviors based on screening questionnaire: taken prescribed antiretroviral medications, OR been told by his/her physician that he/she should be on antiretroviral medications (whether he/she takes them or not); vaginal or anal sex, OR alcohol or drug use. At least one of the 3 aforementioned behaviors are currently at a problem level, based on screening questionnaire: taking currently prescribed antiretroviral medications <90 % of the time in the last month, having unprotected intercourse within the last 3 months, demonstrating problem level alcohol and/or drug use as measured during screening. Able to understand spoken and written English sufficiently to provide consent/assent and be interviewed and participate in study intervention. Not intending to relocate out of the current geographical area for the duration of study participation. Exclusion Criteria: History of any psychiatric thought disorder (e.g., schizophrenia, schizoaffective disorder). Currently involved in behavioral research (assessment or intervention) targeting adherence, sexual risk, or alcohol and/or drug substance abuse OR currently involved in a substance abuse treatment program.

Sites / Locations

  • Children's Hospital of Los Angeles
  • University of Southern California
  • Children's Diagnostic and Teatment Center
  • University of Maryland
  • Children's Hospital of Michigan
  • Children's Hospital of Philadelphia

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Healthy Choices - Motivational Enhancement Intervention

Standard Care

Arm Description

Motivational enhancement intervention

Standard care/individualized referrals

Outcomes

Primary Outcome Measures

Determine the efficacy of a motivational enhancement intervention
The primary objective is to determine the efficacy of a motivational enhancement intervention in reducing health risk behaviors (drug and alcohol use, sexual risk behavior, poor adherence to medications) among HIV+ youth.

Secondary Outcome Measures

Determine the mediators and moderators of the intervention
Determine the mediators (e.g., self-efficacy, stage of change, decisional balance) and moderators (e.g., demographics, emotional distress) of the intervention
Determine secondary intervention effects
Determine secondary intervention effects such as improved health status (through measurements of CD4+ counts and viral load levels), decreased levels of psychological distress, and increased engagement with providers (both medical and ancillary services)
Determine if intervention effects are maintained
Determine if intervention effects are maintained over 12 months post-intervention

Full Information

First Posted
February 9, 2005
Last Updated
March 25, 2019
Sponsor
University of North Carolina, Chapel Hill
Collaborators
National Institute on Drug Abuse (NIDA), National Institute of Mental Health (NIMH), National Institute on Alcohol Abuse and Alcoholism (NIAAA)
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1. Study Identification

Unique Protocol Identification Number
NCT00103532
Brief Title
Healthy Choices to Promote Health and Reduce Risk in HIV-Infected Youth
Official Title
Motivational Enhancement to Promote Health and Reduce Risk in HIV-Infected Youth
Study Type
Interventional

2. Study Status

Record Verification Date
March 2019
Overall Recruitment Status
Completed
Study Start Date
March 2005 (undefined)
Primary Completion Date
March 2008 (Actual)
Study Completion Date
April 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of North Carolina, Chapel Hill
Collaborators
National Institute on Drug Abuse (NIDA), National Institute of Mental Health (NIMH), National Institute on Alcohol Abuse and Alcoholism (NIAAA)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Risk behaviors and their associated adverse health outcomes are becoming increasingly problematic among HIV-infected youth. This study is being conducted to test whether a brief motivational enhancement (ME) intervention will help reduce health risk behaviors (drug and alcohol use, sexual risk behavior, poor adherence to medications) among HIV+ youth.
Detailed Description
Healthy Choices is a randomized clinical trial examining the efficacy of motivational enhancement in reducing risk and promoting healthy behaviors. This study will use a sample of 225 youth (180 after attrition), ages 16-24, of whom 90 will receive the intervention, referral, and standard care, and 90 will receive referral plus standard care. The sample will be drawn from five study sites. Using parallel screening, recruitment will target 100 youth with an adherence problem, 100 youth with a substance use problem, and 25 youth with a sexual risk problem. A repeated measures design will be used for the proposed study. Primary outcome measures are drug and alcohol use, condom use, and HIV medication adherence. Youth will complete an initial data collection session (baseline) during which questionnaire and interview measures will be administered. Blood specimens for viral load and CD4+ count will also be obtained. Randomization procedures will take place after completion of the baseline assessment. Participants who are randomized to the intervention group will participate in four sessions for approximately 3 months and will also receive standard care plus individualized referrals. The control group will receive standard care and individualized referrals. All five sites offer comprehensive, multidisciplinary care including social work and case management services and access to mental health services. Participants will receive a three-month post-test designed to coincide with ME completion. Subsequent post-tests will occur at 6, 9, 12, and 15 months after baseline data collection (3, 6, 9, and 12 months after ME completion).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infection
Keywords
motivational enhancement, health behaviors, risk behaviors

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
225 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Healthy Choices - Motivational Enhancement Intervention
Arm Type
Experimental
Arm Description
Motivational enhancement intervention
Arm Title
Standard Care
Arm Type
Active Comparator
Arm Description
Standard care/individualized referrals
Intervention Type
Behavioral
Intervention Name(s)
Healthy Choices - Motivational Enhancement Intervention
Intervention Description
Participants who are randomized to the intervention group will participate in four sessions (over approximately 3 months) of Healthy Choices; a motivational enhancement intervention specifically designed to target multiple risk behaviors in HIV+ youth. Participants will receive individualized referrals at the fourth session.
Intervention Type
Behavioral
Intervention Name(s)
Standard care
Intervention Description
Participants will receive standard care plus referrals at three months post-baseline
Primary Outcome Measure Information:
Title
Determine the efficacy of a motivational enhancement intervention
Description
The primary objective is to determine the efficacy of a motivational enhancement intervention in reducing health risk behaviors (drug and alcohol use, sexual risk behavior, poor adherence to medications) among HIV+ youth.
Time Frame
15 months
Secondary Outcome Measure Information:
Title
Determine the mediators and moderators of the intervention
Description
Determine the mediators (e.g., self-efficacy, stage of change, decisional balance) and moderators (e.g., demographics, emotional distress) of the intervention
Time Frame
15 months
Title
Determine secondary intervention effects
Description
Determine secondary intervention effects such as improved health status (through measurements of CD4+ counts and viral load levels), decreased levels of psychological distress, and increased engagement with providers (both medical and ancillary services)
Time Frame
15 months
Title
Determine if intervention effects are maintained
Description
Determine if intervention effects are maintained over 12 months post-intervention
Time Frame
15 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
24 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: HIV infection as documented by professional referral and medical record review. HIV+ participants who are self-referred and not in medical care will be required to provide documentation of test results. Males or females between the age of 16 years and 0 days and 24 years and 364 days at the time of study enrollment. Reports having ever engaged in at least 2 of the following 3 behaviors based on screening questionnaire: taken prescribed antiretroviral medications, OR been told by his/her physician that he/she should be on antiretroviral medications (whether he/she takes them or not); vaginal or anal sex, OR alcohol or drug use. At least one of the 3 aforementioned behaviors are currently at a problem level, based on screening questionnaire: taking currently prescribed antiretroviral medications <90 % of the time in the last month, having unprotected intercourse within the last 3 months, demonstrating problem level alcohol and/or drug use as measured during screening. Able to understand spoken and written English sufficiently to provide consent/assent and be interviewed and participate in study intervention. Not intending to relocate out of the current geographical area for the duration of study participation. Exclusion Criteria: History of any psychiatric thought disorder (e.g., schizophrenia, schizoaffective disorder). Currently involved in behavioral research (assessment or intervention) targeting adherence, sexual risk, or alcohol and/or drug substance abuse OR currently involved in a substance abuse treatment program.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sylvie Naar-King, PhD
Organizational Affiliation
Children's Hospital of Michigan
Official's Role
Study Chair
Facility Information:
Facility Name
Children's Hospital of Los Angeles
City
Los Angeles
State/Province
California
ZIP/Postal Code
90027
Country
United States
Facility Name
University of Southern California
City
Los Angeles
State/Province
California
ZIP/Postal Code
90033
Country
United States
Facility Name
Children's Diagnostic and Teatment Center
City
Fort Lauderdale
State/Province
Florida
ZIP/Postal Code
33316
Country
United States
Facility Name
University of Maryland
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21201
Country
United States
Facility Name
Children's Hospital of Michigan
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48201
Country
United States
Facility Name
Children's Hospital of Philadelphia
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
19996045
Citation
Naar-King S, Parsons JT, Murphy DA, Chen X, Harris DR, Belzer ME. Improving health outcomes for youth living with the human immunodeficiency virus: a multisite randomized trial of a motivational intervention targeting multiple risk behaviors. Arch Pediatr Adolesc Med. 2009 Dec;163(12):1092-8. doi: 10.1001/archpediatrics.2009.212.
Results Reference
derived

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Healthy Choices to Promote Health and Reduce Risk in HIV-Infected Youth

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