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Growing Up: Intervening With HIV-Positive Adolescents in Resource-Poor Settings

Primary Purpose

HIV Infection

Status
Completed
Phase
Not Applicable
Locations
Haiti
Study Type
Interventional
Intervention
N'ap Grandi
N'ap Grandi - A
Health Promotion - A
Sponsored by
Florida International University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for HIV Infection focused on measuring Adolescence, Adherence

Eligibility Criteria

15 Years - 19 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. youth aged 15-19 years receiving 1st-line ART for at least 3 months;
  2. exhibiting risk factors of detectable Viral Load and/or unprotected vaginal/anal intercourse in the previous 6 months;
  3. fluent in spoken Haitian Creole which is required to complete assessments and to participate in the intervention groups;
  4. willing to a) assent to study participation if under 18, and b) having a parent or caregiver aged >18 years provide informed consent and participate in the caregiver workshops.

Exclusion Criteria:

  1. cognitively impaired, as determined by the Test of Nonverbal Intelligence (TONI), since such impairment may compromise the ability to comprehend and participate in the assessment and intervention;
  2. exhibits bipolar disorder, psychosis, or current need for inpatient psychiatric hospitalization.

Sites / Locations

  • GHESKIO Centers

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Placebo Comparator

Arm Label

N'ap Grandi

N'ap Grandi - A

Health Promotion - A

Arm Description

Both Adolescent and Caregiver participate in assessment and intervention groups. Adolescent assessments will be administered at baseline, 3 months- and 6 months-post intervention. Caregiver assessments will be administered at baseline and 6 months-post intervention.

Adolescents participate in assessment and intervention groups, Caregivers participate in assessment only. Adolescent assessments will be administered at baseline, 3 months- and 6 months-post intervention. Caregiver assessments will be administered at baseline and 6 months-post intervention.

Adolescents participate in assessment and intervention groups, Caregivers participate in assessment only. Adolescent assessments will be administered at baseline, 3 months- and 6 months-post intervention. Caregiver assessments will be administered at baseline and 6 months-post intervention.

Outcomes

Primary Outcome Measures

ART Adherence and response
Data from self report questionnaire (percent medications taken), medication possession ratio (percent completed), and virologic suppression (percent improvement) will be aggregated into a composite measure of adherence.

Secondary Outcome Measures

HIV sexual transmission risk reduction
Increase in self-reported safer sex behavior via questionnaire
Caregiver supportive communication
Increase in self-reported positive caregiver-adolescent communication and monitoring via questionnaire
Psychosocial health
Improvement in self-reported stress and mood via questionnaire
Cost of intervention from the health center perspective
Provide data on the economic feasibility of broader scale up of these interventions

Full Information

First Posted
September 24, 2016
Last Updated
July 10, 2018
Sponsor
Florida International University
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1. Study Identification

Unique Protocol Identification Number
NCT02921516
Brief Title
Growing Up: Intervening With HIV-Positive Adolescents in Resource-Poor Settings
Official Title
Growing Up: Intervening With HIV-Positive Adolescents in Resource-Poor Settings
Study Type
Interventional

2. Study Status

Record Verification Date
July 2018
Overall Recruitment Status
Completed
Study Start Date
September 2016 (undefined)
Primary Completion Date
May 2018 (Actual)
Study Completion Date
May 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Florida International University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Despite overall declines in HIV incidence and mortality since ART scale-up in low and middle income countries, both have risen among youth. In addition, HIV-infected youth achieve inferior treatment outcomes compared to their adult counterparts in both high- and low-income countries, and these poorer outcomes are generally attributed to suboptimal adherence. Thus, there is a critical need for the development of adherence and risk reduction interventions for the growing cohort of these youth, and the proposed cognitive behavioral N'ap Grandi is one such intervention.
Detailed Description
As pediatric HIV infection has shifted from being a fatal disease to a chronic illness, a growing cohort of young people are moving through adolescence with all the challenges of the adult HIV-infected population but largely without comparable treatment outcomes or an evidence base to improve adherence to antiretroviral treatment (ART) and preventive behavior. Despite overall declines in HIV incidence and mortality since the ART scale-up, both have risen among youth. The goal of the proposed 3-year R34 developmental study is to respond to this need for tailored research, in particular among HIV+ older adolescents, and contribute to understanding the added value in resource-limited settings of including caregivers in an adherence and risk reduction program. Although caregiver involvement is a recognized correlate of outcomes in HIV+ youth, there are no rigorous studies of the role of caregivers in outcomes among HIV+ older adolescents.This project will integrate caregiver involvement and cognitive behavioral intervention (CBI) elements to improve ART adherence and HIV risk reduction for HIV+ older adolescents treated in resource-poor clinical settings.Our proposed study population will include caregivers and 15 to 19 year-old HIV+ youth who know their status and are receiving ART in Port-au-Prince, Haiti. Guided by the theoretical framework of the developmentally sensitive Information-Motivation-Behavioral Skills for Pediatric Adherence (IMB-PED), we will develop Growing Up (N'ap Grandi, in Haitian Creole) as a collaborative model of caregiver-adolescent engagement in the key informational, motivational, and behavioral skills antecedents of ART adherence and risk reduction. The study will utilize qualitative and quantitative methods to: identify barriers and facilitators to adherence and risk reduction (Aim 1); develop and pretest N'ap Grandi, including developmentally-appropriate manuals, training materials, procedures, and psychometric adequacy of measures (Aim 2); and assess feasibility and preliminary efficacy in a 3-arm randomized controlled trial (RCT), in which 120 youth will be assigned to three groups: the experimental caregiver-adolescent N'ap Grandi, an adolescent-only version (N'ap Grandi-A) and an adolescent-only health promotion group (HP-A), examining ART adherence and virologic response, HIV risk behaviors, positive communication and monitoring, stress and mood, and costs from the health center perspective (Aim 3).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infection
Keywords
Adolescence, Adherence

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
278 (Actual)

8. Arms, Groups, and Interventions

Arm Title
N'ap Grandi
Arm Type
Experimental
Arm Description
Both Adolescent and Caregiver participate in assessment and intervention groups. Adolescent assessments will be administered at baseline, 3 months- and 6 months-post intervention. Caregiver assessments will be administered at baseline and 6 months-post intervention.
Arm Title
N'ap Grandi - A
Arm Type
Active Comparator
Arm Description
Adolescents participate in assessment and intervention groups, Caregivers participate in assessment only. Adolescent assessments will be administered at baseline, 3 months- and 6 months-post intervention. Caregiver assessments will be administered at baseline and 6 months-post intervention.
Arm Title
Health Promotion - A
Arm Type
Placebo Comparator
Arm Description
Adolescents participate in assessment and intervention groups, Caregivers participate in assessment only. Adolescent assessments will be administered at baseline, 3 months- and 6 months-post intervention. Caregiver assessments will be administered at baseline and 6 months-post intervention.
Intervention Type
Behavioral
Intervention Name(s)
N'ap Grandi
Intervention Description
Eight 90-minute adolescent cognitive behavioral modules and four 90-minute caregiver cognitive behavioral modules, delivered in weekend workshops over a 1 month period, with the last two modules for joint participation of adolescents and caregivers.
Intervention Type
Behavioral
Intervention Name(s)
N'ap Grandi - A
Intervention Description
Eight 90-minute adolescent cognitive behavioral modules delivered in weekend workshops over a 1 month period.
Intervention Type
Behavioral
Intervention Name(s)
Health Promotion - A
Intervention Description
Eight 90-minute adolescent health promotion modules delivered in weekend workshops over a 1 month period.
Primary Outcome Measure Information:
Title
ART Adherence and response
Description
Data from self report questionnaire (percent medications taken), medication possession ratio (percent completed), and virologic suppression (percent improvement) will be aggregated into a composite measure of adherence.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
HIV sexual transmission risk reduction
Description
Increase in self-reported safer sex behavior via questionnaire
Time Frame
6 months
Title
Caregiver supportive communication
Description
Increase in self-reported positive caregiver-adolescent communication and monitoring via questionnaire
Time Frame
6 months
Title
Psychosocial health
Description
Improvement in self-reported stress and mood via questionnaire
Time Frame
6 months
Title
Cost of intervention from the health center perspective
Description
Provide data on the economic feasibility of broader scale up of these interventions
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
15 Years
Maximum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: youth aged 15-19 years receiving 1st-line ART for at least 3 months; exhibiting risk factors of detectable Viral Load and/or unprotected vaginal/anal intercourse in the previous 6 months; fluent in spoken Haitian Creole which is required to complete assessments and to participate in the intervention groups; willing to a) assent to study participation if under 18, and b) having a parent or caregiver aged >18 years provide informed consent and participate in the caregiver workshops. Exclusion Criteria: cognitively impaired, as determined by the Test of Nonverbal Intelligence (TONI), since such impairment may compromise the ability to comprehend and participate in the assessment and intervention; exhibits bipolar disorder, psychosis, or current need for inpatient psychiatric hospitalization.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jessy G. Dévieux, Ph.D.
Organizational Affiliation
Florida International University
Official's Role
Principal Investigator
Facility Information:
Facility Name
GHESKIO Centers
City
Port-au-Prince
Country
Haiti

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Growing Up: Intervening With HIV-Positive Adolescents in Resource-Poor Settings

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