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Multiple SclerosisNCT07663266

Development of Pain Management JITAI Content in Multiple Sclerosis and Spinal Cord Injury

An observational study of Multiple Sclerosis and Spinal Cord Injury, run by University of Michigan at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Multiple Sclerosis, Spinal Cord Injury
What is being tested?
Push Notification Content
How many people
10 participants
Where
1 siteUnited States
Study dates
15 May 2026to 28 Jul 2026
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Adults with chronic pain and either MS or SCI.

Who may be able to join

  • 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.

Who cannot join

  • Cognitive or other impairment (e.g., hearing) that precludes study participation.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • University of Michigan

    Ann Arbor, Michigan, 48109

Other trials in United States

About this study

Official title: Development of Pain Management Just-In-Time Adaptive Interventions (JITAI) Content in Multiple Sclerosis and Spinal Cord Injury

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.

Being tested
Push Notification Content
Medical subject headings
Multiple Sclerosis, Spinal Cord Injuries

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Push Notification ContentOther

    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.

Study groups in NCT07663266
Study groupRoleWhat they receive
InterviewsThis study will utilize a community engaged research approach to facilitate collaboration between participants and researchers in developing JITAI content to support pain self-management. Participants will have been formally diagnosed with either multiple sclerosis (MS) and/or spinal cord injury (SCI). Participants will review proposed JITAI content and provide feedback only to the study team.
Receives: Other: Push Notification Content

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Preference

    Participant preferences for the JITAI push notification content and delivery assessed via interviews. The primary outcome will be assessed with qualitative data analyses, which will be used to inform push notification content for a JITAI to support chronic pain self-management in adults with MS and adults with SCI.

    Measured: 1 day

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted23 Jun 2026
  2. Study start15 May 2026
  3. Primary completion28 Jul 2026
  4. Study completion28 Jul 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Cross-sectional
Enrolment
10 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07663266
Sponsor's protocol ID
HUM00290625
Other IDs
K24AT012644-02
Status last verified
Aug 2026
First submitted
16 Jun 2026
Last updated
26 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Multiple Sclerosis and Spinal Cord Injury, run by University of Michigan at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 26 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Preference (time frame: 1 day). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Aug 2026; AzTrials last refreshed its copy on 6 Nov 2026.

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