Actively Recruiting

Phase Not Applicable
Age: 18Years - 60Years
All Genders
ID05165927

Comparison of Methods in Post Operative Hip Arthroscopy Rehabilitation Using Blood Flow Restriction Therapy

Led by University of Colorado, Denver · Updated on 2024-12-11

120

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the effectiveness of blood flow restriction (BFR) therapy as part of rehabilitation after hip arthroscopy surgery. The study aims to compare the use of BFR cuffs, provided by the smart training technology company SAGA, added to the current standard of care (SOC) physical therapy for hip arthroscopy recovery. This interventional study focuses on people with specific hip injuries including labral tears and femoroacetabular impingement syndrome. Participants will be randomly assigned to one of two groups: one receiving standard hip arthroscopy rehabilitation and the other receiving the same rehabilitation plus BFR therapy using cuffs during certain exercises. The BFR treatment includes a detailed 12-week exercise protocol with phases involving different exercises and frequencies, starting with six days per week and reducing to three days per week. The BFR cuff is used at 80% limb occlusion pressure for specific exercises at home and supervised clinic visits. After 12 weeks, BFR therapy is discontinued and both groups continue with standard rehabilitation. Participants will be involved in the 12-week treatment protocol beginning the day after surgery and followed for two years for ongoing assessments. They will attend weekly physical therapy visits and perform exercises at home using the BFR cuffs if in the intervention group. Researchers will measure hip extensor strength and other hip muscle strength, physical function, pain, range of motion, activity levels, and resiliency over two years. The study also includes monitoring for safety and progress through physical exams and patient-reported outcomes.

CONDITIONS

Brief Title

Comparison of Methods in Post Operative Hip Arthroscopy Rehabilitation

Who Can Participate

Age: 18Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 to 60 years
  • Patients with labral tears, femoroacetabular impingement syndrome, loose bodies, ligamentum teres tears, or related intra-articular hip pathology treated with hip arthroscopy
  • Access to a smartphone device to use the free SAGA BFR application
Not Eligible

You will not qualify if you...

  • Bilateral hip surgeries planned within 12 weeks of each other
  • Concomitant peri-acetabular osteotomy
  • Soft tissue repairs such as hamstring or gluteal repairs
  • Clinically diagnosed hip dysplasia
  • Contraindications for blood flow restriction including deep vein thrombosis, pulmonary embolism, hemorrhagic or thrombolytic stroke, clotting disorders, hemophilia, or use of blood thinners
  • Pregnant or up to 6 months post-partum
  • Untreated hypertension or hypotension
  • Rhabdomyolysis or recent traumatic injury

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 screening and enrollment visit

Treatment

Duration - 12 weeks

Participants undergo a 12-week post-operative rehabilitation protocol following hip arthroscopy. The experimental group uses blood flow restriction (BFR) cuffs during specific exercises added to standard rehabilitation, while the control group follows standard rehabilitation alone.

Weekly clinic visits with physical therapy and daily or thrice-weekly home exercises depending on phase and group assignment

Follow-up

Duration - Up to 2 years

Participants complete outcome assessments and rehabilitation monitoring extending up to 2 years after surgery to evaluate long-term hip function and strength.

Visits and assessments occur periodically during the 2-year follow-up

Trial Site Locations

Total: 1 location

1

UCHealth Steadman Hawkins Clinic Denver

Englewood, Colorado, United States, 80012

Actively Recruiting

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Research Team

L

Lauren M Heylmun, BS

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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