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The Wise App Trial for Improving Health Outcomes in PLWH (WiseApp)

Primary Purpose

HIV/AIDS

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Wise app with medication adherence reminders
Wise app with fitness reminders
Sponsored by
Columbia University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for HIV/AIDS focused on measuring Wisepill, ART, PLWH

Eligibility Criteria

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

Inclusion Criteria:

  • Have a diagnosis of HIV
  • Report past 30 days adherence of 80% or less as measured using the Visual Analogue Scale (VAS), or have a viral load of over 400 copies/mL
  • Be able to communicate and read in English or Spanish
  • Live in the US
  • Have a smartphone
  • Be taking ART medications

Exclusion Criteria:

  • Participation in any other mobile app study for PLWH, including text messaging studies
  • Diagnosis of a clinical problem that would preclude someone from using a smartphone

Sites / Locations

  • Columbia University Irving Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Sham Comparator

Experimental

Arm Label

Control

Intervention

Arm Description

WiseApp that delivers fitness reminders

WiseApp that delivers medication adherence reminders

Outcomes

Primary Outcome Measures

Change in ART Adherence - Clever Cap
The CleverCapTM dispenser will automatically record each time a participant opens the dispenser. We will collect adherence data each day from the start to the end of trial (day 1 to 6 months), and it is a count response (number of times taking medication each day).

Secondary Outcome Measures

Change in Score on the Center for Adherence Support Evaluation (CASE) Index
The CASE Adherence Index is an easy to administer instrument that provides an alternative method for assessing ART adherence in clinical settings. Items are scored such that higher values indicate better adherence, and the maximum total score is 16. Scores of 11 or higher on this index indicate good adherence (Cronbach's α= 0.79).
Change in CD4 Count
Using blood samples obtained during study visits, CD4 count will be used to asses ART adherence.
Change in Viral Load
Using blood samples obtained during study visits, viral load levels will be used to asses ART adherence.
Change in Number of Primary Care Visits
This will be measured by the self-reported number of primary care visits.
Change in Score on the Engagement with Health Care Provider Scale
The Engagement with Health Care Provider 13-item Scale will be administered over the course of the trial to evaluate how participants' engagement with their health care providers changes their health care access overall. Items are scored such that higher scores indicate a more negative relationship with their health care provider, where the maximum total score is 52.
Change in Score on the Perceived Ease of Use and Potential Usefulness Questionnaire
Technology Acceptance: Perceived Ease of Use and Potential Usefulness 14-item Questionnaire provides a method for assessing participants' perception of the usefulness of the technology. Items are scored such that higher values indicate more positive perception, where the maximum total score is 70.

Full Information

First Posted
May 24, 2017
Last Updated
April 27, 2021
Sponsor
Columbia University
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1. Study Identification

Unique Protocol Identification Number
NCT03205982
Brief Title
The Wise App Trial for Improving Health Outcomes in PLWH
Acronym
WiseApp
Official Title
The Wise App Trial for Improving Health Outcomes in People Living With HIV
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Unknown status
Study Start Date
January 31, 2018 (Actual)
Primary Completion Date
October 31, 2021 (Anticipated)
Study Completion Date
October 31, 2021 (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
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The overall goal of this study is to design a user-centered design app linked to a smart pill box for people living with HIV (PLWH) and evaluate its effects in a randomized controlled trial. The proposed trial is scientifically significant in representing a principled and systematic effort to test the efficacy of a smartphone intervention linked to a smart pill box for antiretroviral (ART) adherence in PLWH in the United States (US). Guided by a strong theoretical framework building on earlier user-centered design work and integrating a real-time monitoring device, this work has the potential to improve ART adherence in PLWH and have a sustainable public health impact.
Detailed Description
Human Immunodeficiency virus (HIV) continues to affect 1.2 million Americans. Achieving viral suppression through adherence to antiretroviral (ART) therapy is a critical determinant of successful transmission prevention and long-term outcomes in HIV-infected patients. However only about 25% of persons living with HIV (PLWH) in the US are virally suppressed, demonstrating the need for effective interventions that enhance ART adherence. mHealth is a tool that has proven useful in supporting behavior change, but most mHealth tools for PLWH have not been well-developed or evaluated. Given the dearth of useful and likeable apps, the need for improving medication adherence in PLWH, and the great promise of mHealth, the investigators propose to build and test a user-centered smartphone app linked to a smart pill box targeting ART adherence in PLWH. Self-report of medication adherence is often criticized since it typically overestimated adherence especially in unmasked trials. Current adherence assessments, such as patient recall, pill counts and pharmacy refill data, typically detect missed doses long after they occur. This study will use real-time, wireless monitoring strategies via the Wisepill dispenser, for measuring ART adherence.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV/AIDS
Keywords
Wisepill, ART, PLWH

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
200 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
Sham Comparator
Arm Description
WiseApp that delivers fitness reminders
Arm Title
Intervention
Arm Type
Experimental
Arm Description
WiseApp that delivers medication adherence reminders
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
Device
Intervention Name(s)
Wise app with fitness reminders
Intervention Description
The control group will receive the Wise app with fitness reminders
Primary Outcome Measure Information:
Title
Change in ART Adherence - Clever Cap
Description
The CleverCapTM dispenser will automatically record each time a participant opens the dispenser. We will collect adherence data each day from the start to the end of trial (day 1 to 6 months), and it is a count response (number of times taking medication each day).
Time Frame
Up to 6 months
Secondary Outcome Measure Information:
Title
Change in Score on the Center for Adherence Support Evaluation (CASE) Index
Description
The CASE Adherence Index is an easy to administer instrument that provides an alternative method for assessing ART adherence in clinical settings. Items are scored such that higher values indicate better adherence, and the maximum total score is 16. Scores of 11 or higher on this index indicate good adherence (Cronbach's α= 0.79).
Time Frame
Baseline, 3 month follow up, and 6 month follow up
Title
Change in CD4 Count
Description
Using blood samples obtained during study visits, CD4 count will be used to asses ART adherence.
Time Frame
Baseline, 3 month follow up, and 6 month follow up
Title
Change in Viral Load
Description
Using blood samples obtained during study visits, viral load levels will be used to asses ART adherence.
Time Frame
Baseline, 3 month follow up, and 6 month follow up
Title
Change in Number of Primary Care Visits
Description
This will be measured by the self-reported number of primary care visits.
Time Frame
Baseline, 3 months, and 6 months
Title
Change in Score on the Engagement with Health Care Provider Scale
Description
The Engagement with Health Care Provider 13-item Scale will be administered over the course of the trial to evaluate how participants' engagement with their health care providers changes their health care access overall. Items are scored such that higher scores indicate a more negative relationship with their health care provider, where the maximum total score is 52.
Time Frame
Baseline, 3 months, and 6 months
Title
Change in Score on the Perceived Ease of Use and Potential Usefulness Questionnaire
Description
Technology Acceptance: Perceived Ease of Use and Potential Usefulness 14-item Questionnaire provides a method for assessing participants' perception of the usefulness of the technology. Items are scored such that higher values indicate more positive perception, where the maximum total score is 70.
Time Frame
Baseline, 3 month follow up and 6 month follow up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Have a diagnosis of HIV Report past 30 days adherence of 80% or less as measured using the Visual Analogue Scale (VAS), or have a viral load of over 400 copies/mL Be able to communicate and read in English or Spanish Live in the US Have a smartphone Be taking ART medications Exclusion Criteria: Participation in any other mobile app study for PLWH, including text messaging studies Diagnosis of a clinical problem that would preclude someone from using a smartphone
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rebecca Schnall, PhD, RN
Organizational Affiliation
Columbia University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Columbia University Irving Medical Center
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33238931
Citation
Flynn G, Jia H, Reynolds NR, Mohr DC, Schnall R. Protocol of the randomized control trial: the WiseApp trial for improving health outcomes in PLWH (WiseApp). BMC Public Health. 2020 Nov 25;20(1):1775. doi: 10.1186/s12889-020-09688-0.
Results Reference
derived
PubMed Identifier
32779730
Citation
Palmer MJ, Henschke N, Villanueva G, Maayan N, Bergman H, Glenton C, Lewin S, Fonhus MS, Tamrat T, Mehl GL, Free C. Targeted client communication via mobile devices for improving sexual and reproductive health. Cochrane Database Syst Rev. 2020 Jul 14;8(8):CD013680. doi: 10.1002/14651858.CD013680.
Results Reference
derived

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The Wise App Trial for Improving Health Outcomes in PLWH

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