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RecruitingKnee OsteoarthritisInsomnia

Move and Snooze: Adding Insomnia Treatment to an Exercise Program to Improve Pain Outcomes in Older Adults With Knee Osteoarthritis

Eligible age

50+ yrs

Accepts

All genders

Locations

1 state

Healthy volunteers

No

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About this study

This research will compare the effectiveness of a remotely delivered personalized exercise coaching plus an evidence-based sleep improvement intervention to remotely delivered personalized exercise coaching alone for knee osteoarthritis pain. The study team hypothesize that the combined intervention will result in greater improvements in patient-reported pain intensity, recorded with real-time data capture, than remotely delivered exercise coaching alone.

Sponsor: University of Michigan

You may qualify if…

  • Self-reported physician diagnosis of knee osteoarthritis
  • Persistent knee osteoarthritis-related pain of at least moderate intensity (as indicated in the protocol)
  • Indication of persistent symptoms of insomnia, determined by scoring on the Sleep Condition Indicator questionnaire (as indicated in the protocol)
  • If receiving medication for pain or sleep disturbances, having had no change in prescription in the previous three months and be willing to make no other changes to medications for pain or sleep during the active study period.
  • Adequate literacy level to ensure web-based surveys can be completed independently, as assessed using a brief 3-item literacy level screener

You may not qualify if…

  • Concurrent diagnosis of a systemic, inflammatory musculoskeletal disorder (e.g., rheumatoid arthritis)
  • Active malignancy
  • Neurological conditions (e.g., movement disorders)
  • Any medical condition which would make graded increase of physical activity unsuitable (determined by a positive answer to the question: "Has a doctor or healthcare professional advised you to avoid physical activity for any reason?").
  • Unable to understand English sufficiently to take part in the intervention.
  • Unable to provide electronic informed consent.
  • Evidence of significant cognitive impairment (i.e., ≥2 errors on a 6-item cognitive screener).
  • Presence of severe psychiatric disorder.

Where it's recruiting

Michigan

Ann Arbor

Source: ClinicalTrials.gov · NCT06580561 · last updated 2026-04-13

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