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ACL Reconstruction Rehabilitation With Exercise and Psychological Support

Study acronym: ACLR-REPS
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 10 months later Nov 30, 2026 → Oct 1, 2027
See other at-risk trials from HealthPartners Institute

Record History

  1. Primary completion pushed from Nov 30, 2026 to Oct 1, 2027 Completion pushed from Aug 31, 2027 to Dec 31, 2027 · Eligibility criteria expanded, about 10 words · Secondary endpoints: details revised at 7 of 7 entries Show 3 more changesShow less
    • Completion pushed from Aug 31, 2027 to Dec 31, 2027
    • Eligibility criteria expanded, about 10 words
    • Secondary endpoints: details revised at 7 of 7 entries
  2. Primary completion pushed from Mar 31, 2026 to Nov 30, 2026v4
  3. Eligibility criteria expanded, about 8 words Secondary endpoints: 6 to 7v3 Show 1 more changeShow less
    • Secondary endpoints: 6 to 7

    See this version in full on ClinicalTrials.gov ↗

  4. Trial status: Not Yet Recruiting to Recruiting Study sites: 0 to 1 · Start date changed from estimate of May 23, 2025 to May 1, 2025v2 Show 2 more changesShow less
    • Study sites: 0 to 1
    • Start date changed from estimate of May 23, 2025 to May 1, 2025
  5. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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 purpose of this study is to examine ACLR Rehabilitation with Exercise and Psychological Support (REPS), comparing two approaches for providing psychological support along with exercise during ACL reconstruction rehabilitation. In one group, physical therapists have received training that may boost emotional support during rehabilitation. In the other group, physical therapists will not have the training. Both groups will get similar exercises and participate in the same testing. Both groups will also watch short videos during rehabilitation that are specific to their group. Participants will not know to which group they are assigned until the end of the study. Participation will attend a total of four study visits over the course of 6 months, including 1 visit before the surgery and 3 visits during follow-up.
Trial Details
NCT Number NCT06991192
Lead Sponsor HealthPartners Institute
Collaborators: National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Conditions Anterior Cruciate Ligament Reconstruction Rehabilitation
Enrollment 60 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov