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Expanding Exercise Programming for Veterans Through Telehealth

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 3 months later Sep 30, 2026 → Dec 31, 2026
See other at-risk trials from VA Office of Research and Development

Record History

  1. Primary completion pushed from Sep 30, 2026 to Dec 31, 2026 Eligibility criteria expanded, about 18 words · Secondary endpoints: details revised at 1 of 1 entry Show 2 more changesShow less
    • Eligibility criteria expanded, about 18 words
    • Secondary endpoints: details revised at 1 of 1 entry
  2. Primary completion pushed from Mar 31, 2026 to Sep 30, 2026 Site contact updatedv6 Show 1 more changeShow less
    • Site contact updated
  3. Re-verified, no change to tracked fieldsv5
  4. Eligibility criteria expanded, about 8 words Site details revisedv4 Show 1 more changeShow less
    • Site details revised

    See this version in full on ClinicalTrials.gov ↗

  5. Re-verified, no change to tracked fieldsv3
  6. Trial status: Not Yet Recruiting to Recruiting Site details revisedv2 Show 1 more changeShow less
    • Site details revised
  7. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The goal of this study is to evaluate the acceptability and feasibility of a group telehealth exercise program for Veterans with lower extremity osteoarthritis (OA). Methods: This is a randomized pilot trial where Veterans (n=50) receive a group telehealth exercise program (3 months), followed by an exercise maintenance phase (6 months) that includes either text messaging alone or text messaging plus group telehealth exercise booster sessions. The primary outcomes for this study are feasibility and acceptability of the intervention. Feasibility will be assessed through number and source of referrals, recruitment, and retention. Acceptability will be assessed through surveys and interviews for participants and providers addressing reasons for participation, satisfaction, perceived appropriateness, and overall experience containing Likert scales and both yes/no and open-ended questions. Exploratory outcomes, assessed at multiple time points during the course of the study, will measure changes in the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) and changes in performance measure and physical activity assessed remotely through individual telehealth sessions. Data will be collected at baseline, 3-, 6-, and 9-month follow-up.
Trial Details
NCT Number NCT05666167
Lead Sponsor VA Office of Research and Development
Conditions Arthritis
Enrollment 50 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov