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Effects of Blood Flow Restriction Training and Instrument-Assisted Soft Tissue Mobilization for Pain, Strength, Range of Motion, and Kinesiophobia Among ACL Reconstruction Patients.

StatusActive, Not Recruiting
PhaseNot applicable
Started
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Record History

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  1. Minor Sponsor refiled this as active, not recruiting (was completed)
    • Primary completion date: Oct 1, 2026 to Sep 30, 2026
    • Study completion date: Oct 5, 2026 to Nov 28, 2026
    • Start date: Jul 22, 2026 to Jun 26, 2026
  2. Minor Trial completed Show 5 more changesShow less
    • Study completion date changed from estimate of Nov 25, 2026 to Oct 5, 2026
    • Primary completion date changed from estimate of Oct 2026 to Oct 1, 2026
    • Start date changed from estimate of Jul 28, 2026 to Jul 22, 2026
    • Eligibility criteria expanded, about 14 words
    • Site details revised
  3. Notable Start date: Jun 12, 2026 to Jul 28, 2026
    • Study completion date: Nov 20, 2026 to Nov 25, 2026
    v3
  4. Notable Recruitment openedv2
  5. Minor 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
This randomized clinical trial aims to compare the effects of Blood Flow Restriction Training (BFR) and Instrument-Assisted Soft Tissue Mobilization (IASTM) on pain, quadriceps muscle strength, knee range of motion (ROM), and kinesiophobia in patients following anterior cruciate ligament reconstruction (ACLR). ACLR patients commonly experience persistent muscle weakness, limited ROM, pain, and fear of movement, which can delay functional recovery and return to activity. A total of 46 participants (8-16 weeks post-ACLR) will be randomly allocated into two groups: a BFR group and an IASTM group. Both groups will receive interventions twice weekly for 8 weeks alongside standard physiotherapy. The BFR group will perform low-load resistance exercises under controlled vascular occlusion, while the IASTM group will receive soft tissue mobilization using specialized instruments combined with conventional rehabilitation. Outcome measures will include quadriceps strength (handheld dynamometer), pain (Numeric Pain Rating Scale), knee ROM (goniometer), and kinesiophobia (Tampa Scale of Kinesiophobia), assessed at baseline and post-intervention. The study aims to determine which intervention provides superior improvements in physical and psychological outcomes during early rehabilitation after ACL reconstruction.
Trial Details
NCT Number NCT07662850
Lead Sponsor Lahore University of Biological and Applied Sciences
Conditions
(from sponsor)
ACL Reconstruction
Related terms Kinesiophobia, Pain
Enrollment 46 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov