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The Impact of Blood Flow Restriction Training in Adolescents After ACL Reconstruction: A Randomized Controlled Trial

The Impact of Blood Flow Restriction Training in Adolescents After ACL Reconstruction: A Randomized Controlled Trial

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05754632
Enrollment
40
Registered
2023-03-06
Start date
2023-06-08
Completion date
2029-05-01
Last updated
2026-01-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anterior Cruciate Ligament Injuries, Knee Injuries, Quadriceps Muscle Atrophy

Keywords

physical therapy, rehabilitation

Brief summary

While there are a number studies that have reported on the use of blood flow restriction training (BFRT) in the adult population, there is limited information about the use of BFRT in the adolescent population. This study aims to evaluate the use of BFRT in conjunction with traditional anterior ligament reconstruction (ACLR) rehabilitation in adolescents. The purpose of this study is to compare the addition of a BFRT based exercise protocol to a standard ACL rehabilitation protocol in adolescents. Does the addition of BFRT-based exercise improve strength, hypertrophy, and patient reported outcomes after ACLR in the adolescent population?

Detailed description

A single randomized control trial will compare the use of exercises augmented with BFRT with quantitative measurements of strength and patient-reported outcomes. A total of 40 youth and adolescent patients undergoing a surgical procedure for ACLR and subsequent physical therapy at our institution will be recruited for this study. Patients will be randomized into one of two groups using computer randomization for allocation: the intervention group receiving BFRT as part of physical therapy, and the control group will follow the institution's standard ACLR rehabilitation protocol. Both groups will follow a time- and criterion-based standardized rehabilitation protocol. The primary outcomes will be isometric and isokinetic knee peak torque and limb symmetry indices. Secondary outcomes will be quadriceps hypertrophy via mid-thigh circumference and patient-reported outcomes. Target Population Adolescent patients between the ages of 12 and 18 will be recruited at the time of surgery, specifically, those that participate in sports who are undergoing primary ACLR reconstruction at Connecticut Children's Study Group and Control Group Inclusion Criteria · Prior to surgery participated in \> 50 hours/year of level I or II sports as defined by Noyes et al and planned to return to prior level. Level I Sports (4-7 days/week) Jumping, hard pivoting, cutting (basketball, volleyball, football, soccer, gymnastics, skiing. wrestling) Running, twisting, turning (racquet sports, baseball, hockey) Level II sports (1-3 days/week) Jumping, hard pivoting, cutting (basketball, volleyball, football, soccer, gymnastics, skiing. wrestling) Running, twisting, turning (racquet sports, baseball, hockey) * Completion of postoperative rehabilitation following standard protocols * Orthopedic surgical intervention and physical therapy completed at Connecticut Children's.

Interventions

The Delfi Tourniquet System is designed to be used in conjunction with exercise. The system automatically determines the degree of occlusion and allows for safe regulation of pressure. Patients will then complete exercises with the use of this device.

Sponsors

University of Connecticut
CollaboratorOTHER
Connecticut Children's Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

A single randomized control trial will compare the use of exercises augmented with BFRT with quantitative measurements of strength and patient-reported outcomes. A total of 40 youth and adolescent patients undergoing a surgical procedure for ACLR and subsequent physical therapy at our institution will be recruited for this study. Patients will be randomized into one of two groups using computer randomization for allocation: the intervention group receiving BFRT as part of physical therapy, and the control group will follow the institution's standard ACLR rehabilitation protocol. Both groups will follow a time- and criterion-based standardized rehabilitation protocol. The primary outcomes will be isometric and isokinetic knee peak torque and limb symmetry indices. Secondary outcomes will be quadriceps hypertrophy via mid-thigh circumference and patient-reported outcomes.

Eligibility

Sex/Gender
ALL
Age
12 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Prior to surgery participated in \>50 hours/year of level I or II sports as defined by Noyes et al and planned to return to prior level. Level I Sports (4-7 days/week) Jumping, hard pivoting, cutting (basketball, volleyball,football, soccer, gymnastics, skiing. wrestling) * Level II sports (1-3 days/week) Jumping, hard pivoting, cutting (basketball, volleyball,football, soccer, gymnastics, skiing. wrestling) * Completion of postoperative rehabilitation following standard protocols * Orthopedic surgical intervention and physical therapy completed at Connecticut Children's.

Exclusion criteria

* An additional lower extremity injury at time of knee injury or previous surgical intervention on the knee (ipsilateral and contralateral) * Multiple ligament ruptures or trauma * Weight bearing restrictions for greater than 4 weeks after surgery due to concomitant pathology such as meniscal root/radial repair, chondral pathology, or multi-ligament pathology * Follow-up surgical procedures including, but not limited to, post-operative arthrofibrosis Inability to attend regular physical therapy sessions (≥80% of patient treatment sessions and all assessment visits * Contraindications to performing BFRT including known history of central or peripheral neurologic impairments, cardiac or metabolic condition or history of deep vein thrombosis (DVT).

Design outcomes

Primary

MeasureTime frameDescription
Isokinetic Hamstring Strength limb symmetry indexChange in strength at 6 months and 9 months post-opHamstring limb symmetry index is calculated by taking the values from outcome 1. \[ ( peak torque quadriceps involved limb (ft/lbs)/ peak torque quadriceps uninvolved limb (ft-lbs))\*100\] as reported by isokinetic dynamometer. This value is expressed as a percentage. 100% would equal perfect symmetry.
Isometric Hamstring Strength Peak TorqueChange in strength at Pre-op, 3 months post-op, 6 months post-op, 9 months post-opIsometric strength testing to measure peak torque hamstring strength (unit: ft-lbs) as reported by isokinetic dynamometer on involved and uninvolved limb.
Isometric Hamstring Strength Limb Symmetry IndexChange in strength at Pre-op, 3 months post-op, 6 months post-op, 9 months post-opHamstring limb symmetry index is calculated by taking the values from outcome 3 \[ ( peak torque hamstring involved limb (ft/lbs) / peak torque hamstring uninvolved limb (ft-lbs))\*100\] as reported by isokinetic dynamometer. This value is expressed as a percentage.100% would equal perfect symmetry.
Isokinetic Quadriceps strengthChange in strength at 6 months and 9 months post-opIsokinetic strength testing to measure peak torque quadriceps strength (unit: ft-lbs) as reported by isokinetic dynamometer on involved and uninvolved limb.
Isokinetic Quadriceps Strength limb symmetry indexChange in strength at 6 months and 9 months post-opQuadriceps limb symmetry index is calculated by taking the values from outcome 1. \[ ( peak torque quadriceps involved limb (ft/lbs)/ peak torque quadriceps uninvolved limb (ft-lbs))\*100\] as reported by isokinetic dynamometer. This value is expressed as a percentage. 100% would equal perfect symmetry.
Isokinetic Hamstrings StrengthChange in strength at 6 months and 9 months post-opIsokinetic strength testing to measure peak torque hamstring strength (unit: ft-lbs) as reported by isokinetic dynamometer on involved and uninvolved limb.
Range of MotionChange in range of motion at Pre-op, 3 months post-op, 6 months post-op, 9 months post-opActive knee range of motion: Knee AROM will be measured in supine position using a goniometer and standardized procedures reported by Norkin and White
Isometric Quad strength Peak TorqueChange in strength at Pre-op, 3 months post-op, 6 months post-op, 9 months post-opIsometric strength testing to measure peak torque quadriceps strength (unit: ft-lbs) as reported by isokinetic dynamometer on involved and uninvolved limb.
Isometric Quadriceps Strength limb symmetry indexChange in strength at Pre-op, 3 months post-op, 6 months post-op, 9 months post-opQuadriceps limb symmetry index is calculated by taking the values from outcome 1. \[ ( peak torque quadriceps involved limb (ft/lbs)/ peak torque quadriceps uninvolved limb (ft-lbs))\*100\] as reported by isokinetic dynamometer. This value is expressed as a percentage. 100% would equal perfect symmetry.

Secondary

MeasureTime frameDescription
Pediatric International Knee Documentation CommitteeTracking change at Pre-op, 3months post-op, 6 months post-op, 9 months post-op. 2 years post-opPatient Reported Outcome Measure- Scores range from 0 points (lowest level of function or highest level of symptoms) to 100 points (highest level of function and lowest level of symptoms).
Knee Outcomes and Osteoarthritis ScaleTracking change at Pre-op, 3months post-op, 6 months post-op, 9 months post-op. 2 years post-opPatient Reported Outcome Measure- The score is a percentage score from 0 to 100, with 0 representing extreme problems and 100 representing no problems. This scoring direction, 100 indicating no problems
Anterior Cruciate Ligament- Return to Sport after InjuryTracking change at Pre-op, 3months post-op, 6 months post-op, 9 months post-op. 2 years post-opPatient Reported Outcome Measure- The scores range from 0 to 100, with higher scores representing patients who are more ready to return to sport
Tegner Activity Scalechanges from pre-operative, 9 months, and 2 years post-operativeTegner activity scale will measure sport level- higher level equals higher sport competitive level
Quadriceps HypertrophyChange in strength at Pre-op, 8 weeks, 3months post-op, 6months, 9 months post-opThigh Circumference measured at location 10cm superior to patella and measured in cm comparing involved to uninvolved lower extremity

Countries

United States

Contacts

Primary ContactAdam P Weaver, PT, DPT
aweaver@connecticutchildrens.org8602840296
Backup ContactArthur Fredericks, MSPT
afredericks@connecticutchildrens.org8602840296

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026