Development of Pain Management JITAI Content in Multiple Sclerosis and Spinal Cord Injury
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Push Notification Content.
- Who it may be relevant to
- Registry conditions: Multiple Sclerosis, Spinal Cord Injury. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Development of Pain Management Just-In-Time Adaptive Interventions (JITAI) Content in Multiple Sclerosis and Spinal Cord Injury
Overview
Just-In-Time Adaptive Interventions (JITAIs) offer a framework for delivering personalized behavioral support using time-varying data to optimize the timing and type of intervention content. This project will develop the foundational components of a JITAI tailored to adults with chronic pain and either MS or SCI by drawing on symptom self-management content from existing programs (PainGuide, MyMSToolkit, and MySCIToolkit). Intervention content and delivery parameters will be refined through stakeholder engagement via structured interviews to ensure relevance, acceptability, and feasibility.
Interventions
- Other Push Notification Content
This project will develop the foundational components of a JITAI (push notification content) tailored to adults with chronic pain and either MS or SCI by drawing on symptom self-management content from existing programs (PainGuide, MyMSToolkit, and MySCIToolkit). Intervention content and delivery parameters will be refined through stakeholder engagement via structured interviews with participants to ensure relevance, acceptability, and feasibility.
Primary outcome measures
- Preference [Time frame: 1 day]
Eligibility criteria
Inclusion criteria
- Able to read and converse fluently in English
- Multiple sclerosis (MS) or Spinal Cord Injury (SCI) diagnosis
- Chronic pain ( ≥ 4 on average using a 0-10 NRS for 3-month duration)
- Access to an internet connected device with a camera and microphone for participating in virtual interview/focus group.
Exclusion criteria
- Cognitive or other impairment (e.g., hearing) that precludes study participation.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Other
Study locations
United States · 1 center
- University of Michigan — Ann Arbor
Identifiers
NCT: NCT07663266 · HUM00290625 · K24AT012644-02