Evaluating and Optimizing Just-In-Time Adaptive Interventions (JITAIs) in a Digital Mental Health Intervention (Wysa for Chronic Pain) for Middle-Aged and Older Adults With Chronic Pain

Status: Recruiting
Location: See location...
Intervention Type: Behavioral, Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The purpose of this research study is to refine customized in-app notifications in order to optimize users' experience with a mobile app called Wysa for Chronic Pain. This app is designed to support people who have chronic pain and who also experience symptoms of depression and/or anxiety. This version of the app is not currently available to the public. Eligible participants will be asked to download and use the Wysa for Chronic Pain study app for several weeks, and to use it as they normally would if they were not part of a research study. At the beginning and end of the study period, participants will be asked to complete brief surveys about their mood, pain, physical function, and sleep. Additionally, a few participants will be asked to share their experience with the study app at the end of the research study in a casual interview using a secure audio/video recorded call. Participating in the interview portion is optional.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 45
Healthy Volunteers: f
View:

• 45 years or older

• At least moderately severe depression and/or anxiety symptoms (Patient Health Questionnaire-9 (PHQ-9) and/or Generalized Anxiety Disorder-7 (GAD-7) score ≥ 10)

• Chronic pain (i.e., pain on most days or every day in the past three months)

Locations
United States
Missouri
Washington University in St. Louis School of Medicine
RECRUITING
St Louis
Contact Information
Primary
Adriana Martin
azmartin@wustl.edu
314-530-9023
Backup
Research Coordinator
314-747-8489
Time Frame
Start Date: 2025-06-02
Estimated Completion Date: 2026-12
Participants
Target number of participants: 1000
Treatments
Experimental: Wysa for Chronic Pain + JITAIs
Participants assigned to the experimental arm will receive access to the Wysa for Chronic Pain app, and the novel JITAIs that are being tested in this study will be incorporated into the app experience.~In an initial 4-week pilot trial, participants in this arm will receive the JITAIs every time the decision rule (i.e., trigger criteria) is satisfied for that respective JITAI. In subsequent 12-week micro-randomized trials, every time the decision rule for a JITAI is satisfied, participants in this arm will be randomized to receive (versus not receive) the respective JITAI.
Active_comparator: Wysa for Chronic Pain without JITAIs
Participants assigned to the control arm will receive access to the Wysa for Chronic Pain app, but the novel JITAIs that are being tested in this study will not be incorporated into the app experience.
Related Therapeutic Areas
Sponsors
Collaborators: Wysa, National Institute of Mental Health (NIMH), Duke University
Leads: Washington University School of Medicine

This content was sourced from clinicaltrials.gov