RENEW: a digital program to help people with axial spondyloarthritis manage energy and symptoms
Official title: Pilot Randomized Controlled Trial of the RENEW Intervention for Axial Spondyloarthritis
Run by University of Michigan · NCT07836374 · Data updated 2026-11-12
A web-based, peer-led program called RENEW is tested to see if people with axial spondyloarthritis can easily use it, like it, and benefit from it in managing fatigue and symptoms.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 40 (estimated) |
| Sponsor | University of Michigan Academic / other |
| Locations | 1 site (Ann Arbor, Michigan) |
| Status | Recruiting |
| Started | October 22, 2026 |
| Main results expected | March 2027 |
| Study ends | May 2027 |
| Registry record updated | October 29, 2026 |
| Trial ID | NCT07836374 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with physician-diagnosed axSpA (including non-radiographic axSpA) who have moderate to severe fatigue and access to internet-enabled devices.
✕Probably not a fit
People without persistent fatigue or who cannot engage with a web-based platform may receive limited or no benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study tests a web-based, peer-led program (RENEW) for adults with axial spondyloarthritis. It focuses on usability, user satisfaction, and impact on symptom burden and energy levels. Participants engage in virtual coaching and complete online assessments to track changes over time. The study emphasizes feasibility and acceptability before broader efficacy testing.
Why it matters
Potential benefit: If successful, the program could help people with axSpA manage fatigue and symptoms through an accessible online platform.
How similar studies have gone: Previous digital and peer-led health interventions have shown promise in chronic inflammatory conditions, though results vary by program and population.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Physician-diagnosed axSpA (including non-radiographic axSpA) * Have moderate to severe fatigue (average of ≥4/7 on the Fatigue Severity Scale) * Access to a computer, tablet, or smartphone with internet connection * Ability to speak and read English * Willingness to participate in virtual Zoom coaching sessions and complete online assessments * Interested in making some changes and trying new ways to improve health and well-being Exclusion Criteria: * Currently enrolled in other clinical trials * Currently undergoing structured rehabilitation or psychological treatment for major depressive disorder * Significant cognitive impairment that would prevent informed consent or participation * Severe psychiatric illness that would contraindicate participation
Where it's running
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University of Michigan
Ann Arbor, Michigan, United States Recruiting
Study contacts
- Principal investigator: Susan Murphy, ScD, OTR — University of Michigan
- Study coordinator: Elizabeth Haro
- Email: elharo@umich.edu
- Phone: 734-998-7124
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.