search
Back to results

Supporting Adolescent Adherence in Vietnam (SAAV) (SAAV)

Primary Purpose

Adolescents, HIV/AIDS, Patient Adherence

Status
Completed
Phase
Not Applicable
Locations
Vietnam
Study Type
Interventional
Intervention
Tailored realtime triggered reminder pkg
Sponsored by
University of New England
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Adolescents focused on measuring adherence, adolescent, HIV/AIDS, Vietnam

Eligibility Criteria

12 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • currently a patient at the Infectious Disease (ID) clinic at National Hospital for Pediatrics (NHP) in Hanoi, Vietnam
  • between 12 and 17 years old of age AND
  • expected to remain in care at the NHP for 7 months minimum
  • currently on ART
  • live in the clinic catchment area
  • willing to provide informed assent, caregiver willing to provide consent
  • identified ás having adherence challenges (CD4, detectable VL, and/or clinician suggestion)

Exclusion Criteria:

  • below the age of 12 years or above the age of 18
  • not currently on ART
  • live outside the clinic catchment area
  • not willing to provide informed assent, caregiver not willing to provide consent

Sites / Locations

  • Institute for Population Health and Development

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Tailored realtime triggered reminder pkg

Control

Arm Description

The core intervention will utilize innovative wireless technology to provide patients with 1) real time, personalized wireless reminder messages when ART doses are not taken on time, and 2) 'feedback' on adherence behavior via monthly interactive counseling sessions informed by summaries of their previous month's behavior. The core intervention will be personalized by each intervention arm patient, who may choose features to suit their preferences.

Comparison subjects will receive usual care and an offer of counseling at monthly clinic visits.

Outcomes

Primary Outcome Measures

Optimal on-time adherence
Proportion of patients with ≥95% on-time adherence at end of 6-month intervention period in each study arm

Secondary Outcome Measures

CD4 count
Mean change in CD4 count in each study arm
Viral load
Percent of patients with undetectable viral load (UDVL) in each study arm

Full Information

First Posted
January 21, 2017
Last Updated
April 2, 2020
Sponsor
University of New England
Collaborators
Institute of Population, Health and Development, Vietnam, Boston University
search

1. Study Identification

Unique Protocol Identification Number
NCT03031197
Brief Title
Supporting Adolescent Adherence in Vietnam (SAAV)
Acronym
SAAV
Official Title
The Supporting Adolescent Adherence in Vietnam (SAAV) Study
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
May 15, 2017 (Actual)
Primary Completion Date
May 25, 2018 (Actual)
Study Completion Date
May 25, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of New England
Collaborators
Institute of Population, Health and Development, Vietnam, Boston University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No

5. Study Description

Brief Summary
The small RCT will assess feasibility, acceptability, and impact of a real-time intervention on ART adherence and clinical outcomes for HIV-positive adolescents. All subjects will use a wireless pill container (WPC) to monitor adherence. Intervention subjects will receive a personalized triggered reminder (cellphone message/call or bottle-based flash/alarm) when they miss a dose, and engage in monthly counseling sessions informed by their adherence data. Comparison subjects will receive usual care and an offer of counseling at monthly clinic visits.
Detailed Description
A major priority in HIV care and treatment is identifying effective interventions for adolescent patients, including those that make use of new technologies, to help them achieve and maintain high levels of adherence to antiretroviral treatment (ART), particularly as they take responsibility for their own medication-taking in the transition to adult care. The research planned here will contribute to the scientific evidence base on approaches to support ART adherence effectively among youth by 1) conducting formative research on adherence challenges among adolescents and refining options for a personalized adherence intervention package; and 2) implementing a small randomized controlled trial (RCT) to assess the feasibility, acceptability, and efficacy of a novel real-time feedback intervention that permits adolescent patients to tailor intervention features to suit their individual preferences.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Adolescents, HIV/AIDS, Patient Adherence
Keywords
adherence, adolescent, HIV/AIDS, Vietnam

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Masking Description
Open Label
Allocation
Randomized
Enrollment
81 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Tailored realtime triggered reminder pkg
Arm Type
Experimental
Arm Description
The core intervention will utilize innovative wireless technology to provide patients with 1) real time, personalized wireless reminder messages when ART doses are not taken on time, and 2) 'feedback' on adherence behavior via monthly interactive counseling sessions informed by summaries of their previous month's behavior. The core intervention will be personalized by each intervention arm patient, who may choose features to suit their preferences.
Arm Title
Control
Arm Type
No Intervention
Arm Description
Comparison subjects will receive usual care and an offer of counseling at monthly clinic visits.
Intervention Type
Combination Product
Intervention Name(s)
Tailored realtime triggered reminder pkg
Other Intervention Name(s)
wireless monitoring/feedback, counseling, dose histories
Intervention Description
Core intervention: 1) real time, personalized wireless reminder messages when ART doses are not taken on time, and 2) 'feedback' on adherence behavior via monthly interactive counseling sessions informed by summaries of their previous month's behavior. Personalized features of the intervention will be selected by each patient and may include 1) reminders sent to the WPC (light or chimes) or to patient's or caregiver's cell phone if dose is late; 2) content of text messages from a menu of options; 3) use of "youth-friendly" WPC adherence reports for interactive counseling sessions; 4) additional counseling by clinic staff; 5) a "buddy" system, by choosing someone to review the adherence report with him/her; and 6) a "reward message" after a pre-selected time period of excellent adherence.
Primary Outcome Measure Information:
Title
Optimal on-time adherence
Description
Proportion of patients with ≥95% on-time adherence at end of 6-month intervention period in each study arm
Time Frame
End of intervention period (month 7)
Secondary Outcome Measure Information:
Title
CD4 count
Description
Mean change in CD4 count in each study arm
Time Frame
Pre-intervention month (month 1) vs. last intervention month (month 7)
Title
Viral load
Description
Percent of patients with undetectable viral load (UDVL) in each study arm
Time Frame
End of intervention period (month 7)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: currently a patient at the Infectious Disease (ID) clinic at National Hospital for Pediatrics (NHP) in Hanoi, Vietnam between 12 and 17 years old of age AND expected to remain in care at the NHP for 7 months minimum currently on ART live in the clinic catchment area willing to provide informed assent, caregiver willing to provide consent identified ás having adherence challenges (CD4, detectable VL, and/or clinician suggestion) Exclusion Criteria: below the age of 12 years or above the age of 18 not currently on ART live outside the clinic catchment area not willing to provide informed assent, caregiver not willing to provide consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mary DeSilva, ScD
Organizational Affiliation
University of New England
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institute for Population Health and Development
City
Hanoi
Country
Vietnam

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
Undecided.
Citations:
PubMed Identifier
30819228
Citation
DeSilva M, Vu CN, Bonawitz R, Hai LT, Van Lam N, Yen LT, Gifford AL, Haberer J, Linh DT, Sabin L. The Supporting Adolescent Adherence in Vietnam (SAAV) study: study protocol for a randomized controlled trial assessing an mHealth approach to improving adherence for adolescents living with HIV in Vietnam. Trials. 2019 Feb 28;20(1):150. doi: 10.1186/s13063-019-3239-1.
Results Reference
derived

Learn more about this trial

Supporting Adolescent Adherence in Vietnam (SAAV)

We'll reach out to this number within 24 hrs