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Adherence Interventions for HIV Youth Via Text & Cell Phone - Sequential Multiple Assignment Randomized Trial (SMART) (SMART)

Primary Purpose

HIV Infections

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
CPS
SMS
Sponsored by
Florida State University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for HIV Infections focused on measuring Interventions, youth living with HIV, mHealth, ART adherence, adaptive intervention, cell phone, text messaging

Eligibility Criteria

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

Inclusion Criteria:

  • HIV diagnosis
  • Viral load ≥ 200 copies/mL within 3 months prior to enrollment or self-reported adherence ≤ 80%
  • ART medication regimen prescribed minimum of 3 months prior to eligibility VL or self-reported adherence
  • Sole owner of device capable of sending/receiving calls and text messages
  • Willingness to permit research team to communicate with their HIV care provider team

Exclusion Criteria:

  • Mental, physical, or emotional capacity prevents completion of protocol as written
  • Inability to understand written/spoken English
  • Concurrent participant in any adherence behavioral research intervention

Sites / Locations

  • The City University of New York

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm 7

Arm 8

Arm Type

Active Comparator

Active Comparator

Active Comparator

Active Comparator

Active Comparator

Active Comparator

Active Comparator

Active Comparator

Arm Label

CPS-Rsp-T

CPS-Rsp-SC

CPS-NRsp-I

CPS-NRsp-SMS-I

SMS-Rsp-T

SMS-Rsp-SC

SMS-NRsp-CPS-I

SMS-NRsp-I

Arm Description

After 3 months of intervention, this group of CPS Rsp will receive 3 months of CPS-T intervention followed by SC.

After 3 months of intervention, this group of CPS Rsp's intervention will discontinue and they'll receive SC only

After 3 months of intervention, this group of CPS NRsp will receive 3 months of CPS-I followed by 3 months of CPS-T and 3 months of SC.

After 3 months of intervention, this group of CPS NRsp will receive 3 months of SMS-I followed by 3 months of SMS-T and 3 months of SC

After 3 months of intervention, this group of SMS Rsp will receive 3 months of SMS tapered (SMS-T) intervention followed by SC.

After 3 months of intervention, this group of SMS Rsp, intervention will discontinue and they'll receive SC only

After 3 months of intervention, this group of SMS NRsp will receive 3 months of CPS-I followed by 3 months CPS-T and 3 months SC

After 3 months of intervention, this group of SMS NRsp will receive 3 months of SMS-I followed by 3 months of SMS-T and 3 months of SC

Outcomes

Primary Outcome Measures

Viral Load Comparison
Viral Load (VL) suppression rate will be compared between the CPS and SMS groups using an X2 test. Also the drop in VL will be compared between the two groups.

Secondary Outcome Measures

Medication Adherence Rate
Medication adherence rates will be compared between CPS and SMS groups, focusing on non-responders.

Full Information

First Posted
April 12, 2018
Last Updated
July 5, 2022
Sponsor
Florida State University
Collaborators
Children's Hospital Los Angeles, Hunter College of City University of New York, Wayne State University
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1. Study Identification

Unique Protocol Identification Number
NCT03535337
Brief Title
Adherence Interventions for HIV Youth Via Text & Cell Phone - Sequential Multiple Assignment Randomized Trial (SMART)
Acronym
SMART
Official Title
Adaptive Antiretroviral Therapy Adherence Interventions for Youth Living With HIV Through Text Messaging and Cell Phone Support Embedded Within the Sequential Multiple Assignment Randomized Trial (SMART) Design
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Completed
Study Start Date
September 1, 2018 (Actual)
Primary Completion Date
May 31, 2022 (Actual)
Study Completion Date
May 31, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Florida State University
Collaborators
Children's Hospital Los Angeles, Hunter College of City University of New York, Wayne State University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The purpose of this study is to test an adaptive adherence intervention, which utilizes two mobile health (mHealth) intervention designs, in an effort to promote adherence to antiretroviral therapy (ART) and achieve and maintain viral load (VL) suppression in youth living with HIV (YLH) while increasing understanding of the context for wide-scale implementation of cell phone support (CPS) and text messaging support (SMS), with and without incentives.
Detailed Description
The study will consist of two points of randomization. The first step involves randomization of participants to receive either CPS or SMS using a 1:1 allocation ratio. Both intervention conditions will receive 3 months of intervention (i.e., 12 weeks of CPS or SMS). The second step involves a stratified randomization in blocks with 8 possible intervention trajectories. Within each condition, participants are categorized into two groups - responders with VL<200 (Rsp) and non-responders with VL ≥200 (NRsp). Responders in the CPS condition will be randomly assigned to receive either 3 months of CPS tapered (CPS-T) intervention followed by standard care (SC) or only SC. Similarly, responders in the SMScondition will be randomly assigned to receive either 3 months of SMS tapered (SMS-T) intervention followed by SC or only SC. Non-responders in both CPS and SMS conditions will be randomly assigned to receive either 3 months of incentivized CPS (CPS-I) followed by 3 months of CPS-T and 3 months of SC or 3 months of incentivized SMS (SMS-I) followed by 3 months of SMS-T and 3 months of SC.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
Interventions, youth living with HIV, mHealth, ART adherence, adaptive intervention, cell phone, text messaging

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Sequential Assignment
Model Description
Multiple Assignment Randomized Trial
Masking
None (Open Label)
Allocation
Randomized
Enrollment
83 (Actual)

8. Arms, Groups, and Interventions

Arm Title
CPS-Rsp-T
Arm Type
Active Comparator
Arm Description
After 3 months of intervention, this group of CPS Rsp will receive 3 months of CPS-T intervention followed by SC.
Arm Title
CPS-Rsp-SC
Arm Type
Active Comparator
Arm Description
After 3 months of intervention, this group of CPS Rsp's intervention will discontinue and they'll receive SC only
Arm Title
CPS-NRsp-I
Arm Type
Active Comparator
Arm Description
After 3 months of intervention, this group of CPS NRsp will receive 3 months of CPS-I followed by 3 months of CPS-T and 3 months of SC.
Arm Title
CPS-NRsp-SMS-I
Arm Type
Active Comparator
Arm Description
After 3 months of intervention, this group of CPS NRsp will receive 3 months of SMS-I followed by 3 months of SMS-T and 3 months of SC
Arm Title
SMS-Rsp-T
Arm Type
Active Comparator
Arm Description
After 3 months of intervention, this group of SMS Rsp will receive 3 months of SMS tapered (SMS-T) intervention followed by SC.
Arm Title
SMS-Rsp-SC
Arm Type
Active Comparator
Arm Description
After 3 months of intervention, this group of SMS Rsp, intervention will discontinue and they'll receive SC only
Arm Title
SMS-NRsp-CPS-I
Arm Type
Active Comparator
Arm Description
After 3 months of intervention, this group of SMS NRsp will receive 3 months of CPS-I followed by 3 months CPS-T and 3 months SC
Arm Title
SMS-NRsp-I
Arm Type
Active Comparator
Arm Description
After 3 months of intervention, this group of SMS NRsp will receive 3 months of SMS-I followed by 3 months of SMS-T and 3 months of SC
Intervention Type
Behavioral
Intervention Name(s)
CPS
Intervention Description
Assessment of participant's medication adherence and barrier problem solving via phone conversation
Intervention Type
Behavioral
Intervention Name(s)
SMS
Intervention Description
Participants will receive a text message, which will be an electronic reminder regarding medication adherence. Participants will then text back a confirmatory response.
Primary Outcome Measure Information:
Title
Viral Load Comparison
Description
Viral Load (VL) suppression rate will be compared between the CPS and SMS groups using an X2 test. Also the drop in VL will be compared between the two groups.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Medication Adherence Rate
Description
Medication adherence rates will be compared between CPS and SMS groups, focusing on non-responders.
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
15 Years
Maximum Age & Unit of Time
24 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: HIV diagnosis Viral load ≥ 200 copies/mL within 3 months prior to enrollment or self-reported adherence ≤ 80% ART medication regimen prescribed minimum of 3 months prior to eligibility VL or self-reported adherence Sole owner of device capable of sending/receiving calls and text messages Willingness to permit research team to communicate with their HIV care provider team Exclusion Criteria: Mental, physical, or emotional capacity prevents completion of protocol as written Inability to understand written/spoken English Concurrent participant in any adherence behavioral research intervention
Facility Information:
Facility Name
The City University of New York
City
New York
State/Province
New York
ZIP/Postal Code
10018
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
30573448
Citation
Belzer ME, MacDonell KK, Ghosh S, Naar S, McAvoy-Banerjea J, Gurung S, Cain D, Fan CA, Parsons JT. Adaptive Antiretroviral Therapy Adherence Interventions for Youth Living With HIV Through Text Message and Cell Phone Support With and Without Incentives: Protocol for a Sequential Multiple Assignment Randomized Trial (SMART). JMIR Res Protoc. 2018 Dec 20;7(12):e11183. doi: 10.2196/11183.
Results Reference
derived

Learn more about this trial

Adherence Interventions for HIV Youth Via Text & Cell Phone - Sequential Multiple Assignment Randomized Trial (SMART)

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