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Community Health Worker And MHealth to ImProve Viral Suppression (CHAMPS Pilot) (CHAMPS Pilot)

Primary Purpose

HIV/AIDS

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Wise App with medication adherence reminders
CHW Sessions
Sponsored by
Columbia University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV/AIDS focused on measuring ART, PLWH, HIV Infections, Acquired Immunodeficiency Syndrome

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Able to speak, read, and write in English or Spanish; Aged ≥18 years; Willing to provide a valid form of identification for verification; Willing to participate in any assigned arm of the intervention; Having been diagnosed with HIV ≥6 months ago; Have an HIV-1 RNA level >50 copies/mL, or report either not being virally suppressed in the past 12 months or being virally unsuppressed in the past 12 months; Own a smartphone; Ability and willingness to provide informed consent for study participation and consent for access to medical records; and Live in the United States Exclusion Criteria: Reside in a nursing home, prison, and/or receiving in-patient psychiatric care at time of enrollment; Terminal illness with life expectancy <3 months; Planning to move out of the country in the next 3months.

Sites / Locations

  • Columbia University School of NursingRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention or CHAMPS

Control

Arm Description

Wise App that delivers medication adherence reminders and community health worker sessions

Standard of care

Outcomes

Primary Outcome Measures

Change in Viral Load
Using dried blood spot samples or electronic health records obtained during study visits, viral load levels will be used to asses ART adherence.

Secondary Outcome Measures

Change in ART adherence - CleverCap
The CleverCapTM dispenser will automatically record each time a participant opens the dispenser. The investigators will collect adherence data each day from the start to the end of trial (day 1 to 3 months), and it is a count response (number of times taking medication each day).
Change in Score on the Self-Rating Scale Item (SRSI)
The Self-Rating Scale Item is a single-item self-report adherence measure that uses a 5-point Likert scale to describe medication adherence over the past 4 weeks. Scores range from 1(very poor) to 6 (excellent).

Full Information

First Posted
June 26, 2023
Last Updated
August 3, 2023
Sponsor
Columbia University
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1. Study Identification

Unique Protocol Identification Number
NCT05938413
Brief Title
Community Health Worker And MHealth to ImProve Viral Suppression (CHAMPS Pilot)
Acronym
CHAMPS Pilot
Official Title
Community Health Worker And MHealth to ImProve Viral Suppression (CHAMPS Pilot)
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 20, 2023 (Actual)
Primary Completion Date
January 2024 (Anticipated)
Study Completion Date
July 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Columbia 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 overall goal of this study is to evaluate the feasibility of a remotely delivered CHAMPS intervention for people living with HIV (PLWH) in a randomized controlled trial. The proposed trial is scientifically significant in representing a principled and systematic effort to test the efficacy of a combined community health worker (CHW) and smartphone intervention linked to a smart pill box for antiretroviral (ART) adherence in PLWH in the United States (US). Guided by a rigorous theoretical model of supportive accountability and building on preliminary work, this intervention has the potential to enable PLWH to self-manage their ART regimens while CHW monitor their ART adherence in real-time ultimately leading to viral suppression and ART adherence.
Detailed Description
Persons living with HIV (PLWH) now achieve a near-normal life expectancy due to antiretroviral therapy (ART) which has transformed HIV from a terminal diagnosis to a manageable chronic condition. Despite widespread availability of ART in the United States (US), many of the country's approximate 1.1 million PLWH are not fully benefitting from ART due to poor adherence. These suboptimal HIV health outcomes occur at a time when clinicians have limited time and the US healthcare system remains fragmented, further exacerbating the challenges inherent in the lives of underserved, marginalized groups, such as PLWH. Therefore, the development and evaluation of interventions using a cadre of community health workers (CHW) holds promise for addressing these challenges in the US. This study addresses limitations in current research on CHW interventions to improve viral suppression and ART adherence. The ubiquitous nature of mHealth technologies in daily life creates opportunities for health behavior management tools that were not previously possible and has the potential to address many of the healthcare needs of PLWH. The investigators propose to build on strong preliminary data to strengthen a community health worker (CHW) intervention using an existing mHealth approach, and provide further information regarding the successful wide-scale implementation of this combination intervention.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV/AIDS
Keywords
ART, PLWH, HIV Infections, Acquired Immunodeficiency Syndrome

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention or CHAMPS
Arm Type
Experimental
Arm Description
Wise App that delivers medication adherence reminders and community health worker sessions
Arm Title
Control
Arm Type
No Intervention
Arm Description
Standard of care
Intervention Type
Device
Intervention Name(s)
Wise App with medication adherence reminders
Intervention Description
The Intervention group will receive the Wise App that delivers medication adherence reminders.
Intervention Type
Behavioral
Intervention Name(s)
CHW Sessions
Intervention Description
The Intervention group will complete sessions with a community health worker (CHW).
Primary Outcome Measure Information:
Title
Change in Viral Load
Description
Using dried blood spot samples or electronic health records obtained during study visits, viral load levels will be used to asses ART adherence.
Time Frame
Screening, Baseline (not required if a screening visit was completed), 3 month follow up
Secondary Outcome Measure Information:
Title
Change in ART adherence - CleverCap
Description
The CleverCapTM dispenser will automatically record each time a participant opens the dispenser. The investigators will collect adherence data each day from the start to the end of trial (day 1 to 3 months), and it is a count response (number of times taking medication each day).
Time Frame
Up to 3 months
Title
Change in Score on the Self-Rating Scale Item (SRSI)
Description
The Self-Rating Scale Item is a single-item self-report adherence measure that uses a 5-point Likert scale to describe medication adherence over the past 4 weeks. Scores range from 1(very poor) to 6 (excellent).
Time Frame
3 month follow up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Able to speak, read, and write in English or Spanish; Aged ≥18 years; Willing to provide a valid form of identification for verification; Willing to participate in any assigned arm of the intervention; Having been diagnosed with HIV ≥6 months ago; Have an HIV-1 RNA level >50 copies/mL, or report either not being virally suppressed in the past 12 months or being virally unsuppressed in the past 12 months; Own a smartphone; Ability and willingness to provide informed consent for study participation and consent for access to medical records; and Live in the United States Exclusion Criteria: Reside in a nursing home, prison, and/or receiving in-patient psychiatric care at time of enrollment; Terminal illness with life expectancy <3 months; Planning to move out of the country in the next 3months.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rebecca Schnall, PhD, MPH, RN
Phone
212-342-6886
Email
rb897@cumc.columbia.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Shivesh Shourya, BS
Phone
212-342-6984
Email
ss6775@cumc.columbia.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rebecca Schnall, PhD, MPH, RN
Organizational Affiliation
Columbia University School of Nursing
Official's Role
Principal Investigator
Facility Information:
Facility Name
Columbia University School of Nursing
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shivesh Shourya, BS
Phone
212-342-6984
Email
ss6775@cumc.columbia.edu
First Name & Middle Initial & Last Name & Degree
Olivia Wood, MPH
Phone
212-305-8198
Email
orw2104@cumc.columbia.edu
First Name & Middle Initial & Last Name & Degree
Rebecca Schnall, PhD, MPH, RN

12. IPD Sharing Statement

Plan to Share IPD
No

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Community Health Worker And MHealth to ImProve Viral Suppression (CHAMPS Pilot)

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