Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07131787

Optimizing Rehabilitation After Achilles Tendon Rupture Repair: The Role of Blood Flow Restriction Training in Tendon and Muscle Recovery

Led by University Hospital, Ghent · Updated on 2025-09-23

82

Participants Needed

2

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating whether adding blood flow restriction (BFR) therapy to conventional rehabilitation improves recovery for adult patients who have undergone surgical repair for Achilles tendon rupture. The study aims to find out if BFR enhances functional recovery, muscle strength, and tendon healing compared to standard rehabilitation methods. Participants will be randomly assigned to one of two groups starting four weeks after surgery: one group will follow a 24-week standard strength training program, and the other will follow the same program combined with BFR using an occlusion cuff during exercises targeting the quadriceps and calf muscles. The control group will perform the same exercises without the cuff. Throughout the study, participants will attend follow-up visits at weeks 4, 8, 12, 18, 24, and 52. Assessments will include questionnaires about pain, quality of life, fear of movement, and return to sport, as well as medical imaging like ultrasound, MRI, shear wave elastography, and power Doppler. Muscle strength testing and blood samples will also be collected, along with tendon tissue taken during surgery. The main outcome measured is the Achilles tendon rupture score (ATRS) over six months and at one year post-operation.

CONDITIONS

Brief Title

Optimizing Rehabilitation After Achilles Tendon Rupture Repair: The Role of Blood Flow Restriction Training in Tendon and Muscle Recovery

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with total midrupture Achilles tendon rupture
  • Surgical treatment received
  • Older than 18 years
  • Able to understand and speak Dutch
Not Eligible

You will not qualify if you...

  • Bilateral Achilles tendon rupture
  • Previous Achilles tendon rupture
  • Previous treatment with fluoroquinolones or cortisone
  • Other condition in either leg limiting ability to perform exercises or evaluations
  • Diabetes or rheumatic diseases
  • History of deep venous thrombosis
  • Severe cardiovascular disease

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 24 weeks (6 months post-operative)

Participants undergo a strength training rehabilitation program after Achilles tendon rupture repair. One group uses blood flow restriction cuffs during exercises targeting quadriceps and calf muscles, while the other group follows standard strength training without a cuff.

Multiple visits for assessments at weeks 0, 4, 8, 12, 18, and 24

Follow-up

Duration - Up to week 52 (1 year post-operative)

Participants are monitored for recovery progress and tendon health after treatment completion.

Visits at week 52 for follow-up assessments

Trial Site Locations

Total: 2 locations

1

Ghent University

Ghent, East-Flanders, Belgium, 9000

Not Yet Recruiting

2

Ghent University Hospital

Ghent, Belgium, 9000

Actively Recruiting

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Research Team

S

Sarah VanDen Berghe

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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