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Blood Flow Restriction Training (BFR) in an Adolescent Population

A Determination of Efficacy and Therapeutic Benefits of Blood Flow Restriction Training in an Adolescent Population

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04285879
Enrollment
47
Registered
2020-02-26
Start date
2020-12-15
Completion date
2023-10-16
Last updated
2024-07-17

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

Conditions

ACL Injury, ACL Tear, Blood Flow Restriction

Keywords

physical therapy, rehabilitation

Brief summary

While there are a number studies that have reported on the use of BFR in the adult population, there is limited information about the use of BFR in the adolescent population. This study aims to evaluate the use of BFR training in conjunction with traditional ACL (anterior cruciate ligament) reconstruction rehabilitation in adolescents. The purpose of this study is to evaluate the addition of BFR-based exercise to traditional methods of physical therapy. Does the use of BFR-based exercise improve strength, hypertrophy, functional and patient reported outcomes after ACL Reconstruction in the adolescent population?

Detailed description

The planned pilot study is a prospective case control study utilizing retrospective controls. The investigators will compare the use of exercises augmented with BFR with quantitative measurements of strength and patient reported outcomes. A total of 20 youth and adolescent patients undergoing a surgical procedure for ACL reconstruction at Connecticut Children's Elite Sports Medicine and completing physical therapy at Connecticut Children's Sports Physical Therapy will be recruited for this study. A review of data from 20 previous patients, matched for age, sex, BMI and surgical procedure that completed physical therapy at Connecticut Children's Sports Physical Therapy will be used as a comparison. As part of this pilot study, the investigators will additionally collect prospective controls. This population will be patients not participating in physical therapy at Connecticut Children's, but underwent ACL reconstruction by Elite Sports Medicine. The investigators are unsure of the ability for us to collect prospective controls in a timely manner, hence the investigators will use the above described retrospective cohort as controls if the prospective controls prove difficult to recruit. Identification and Recruitment: All potential patients undergoing ACL reconstruction at Elite Sports Medicine will be approached for participation for this study. Eligible patients will be identified at their initial pre-operative appointment with the Sports Medicine Physician, Athletic Trainer, and Sports Physical Therapy Physical Therapist. Subject selection will be completed by those patients meeting the above outlined inclusion and exclusion criteria. At this time, the study purpose and protocol will be explained and a brief summary of the study will be provided. Consent: Consent will take place at the pre-operative visit. The patient/parent will be given a detailed description of the purpose and methodology for this study. The participants will have the opportunity to read the consent forms and ask any questions they may have about the research. If the patients agree to participate, they will be asked to sign the consent form and a copy will be provided. Retention: Eligible patients will be required to be seen for a minimum of 90% of patient visits to be included in this study. In addition to the standard ACL protocol, patients in this study will utilize the Owen Recovery Science exercise protocol for BFR \[18\]. The following guidelines will be followed concerning exercise progression, occlusion pressure and difficulties with volume achievement. To determine the appropriate resistance for each exercise, the patient's 1 repetition maximum (1RM) will be attained using a repetition test \[19\]. This test will use a previously validated algorithm to determine the 1RM based on the weight used to perform a 7-10 repetition test \[20\]. Patient will perform the exercise with a weight they can comfortably lift for several repetitions. Based on the weight or resistance used, and the patient's perceived exertion a 1RM will be estimated using the modified OMNI-RES (OMNI perceived exertion scale for resistance). The starting load for each exercise will be 20-30% of their 1RM , or bodyweight resistance will be used when loading is not feasible. Proposed Protocol Phase 1- Weeks 1 to 2 * Quad Set: 10 second on, 10 second rest at 100% occlusion x10' o progress to isometrics at the edge of the table 60 degrees as clinically appropriate * Side Lying Hip Abduction, 30/15/15/15, at 80% occlusion * Hip Extension from prone 30/15/15/15, at 80% occlusion * Re-check load at the start of each Phase, to determine 1 RM (7-10 RM (repetition maximum) test on leg press) * Total BFR time approximately 24 minutes per session, with 2 sessions per week Phase 2- Weeks 3 to 4 * Replace Quad Set with Long Arc Quad (90-30deg), 30/15/15/15 at 80% occlusion * Replace Hip Extension with Leg Press (shuttle), 30/15/15/15 at 80% occlusion * Hip Abduction, 30/15/15/15 at 80% occlusion * Total BFR time approximately 24 minutes per session with 2 sessions per week Phase 3- Weeks 5 to 6 * Long Arc Quad (90-30deg), 30/15/15/15 at 80% occlusion * Leg Press (shuttle), 30/15/15/15 at 80% occlusion * Replace Hip Abduction with Bilateral Hip Bridge, 30/15/15/15 at 80% occlusion * Total BFR time approximately 24 minutes per session, with 2 sessions per week Phase 4- Weeks 7 to 8 * Leg Press (shuttle), 30/15/15/15 at 80% occlusion * Replace Long Arc Quad with Step Up 30/15/15/15 at 80% occlusion * Bilateral Hip Bridge, 30/15/15/15 at 80% occlusion * Total BFR time approximately 24 minutes per session, with 2 sessions per week Phase 5- Weeks 9 to 12 * Replace Bilateral Hip Bridge with Medial Step Down, 30/15/15/15 at 80% occlusion * Replace Step up with Split Squat, 30/15/15/15 at 80% occlusion * Leg Press (shuttle), 30/15/15/15 at 80% occlusion * Total BFR time approximately 24 minutes per session, with 2 sessions per week Phase 6- Weeks 11 to 12 * Progressively load exercises from phase 5 * Total BFR time approximately 24 minutes per session, with 2 sessions per week

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 following the Owens Recovery Science Protocol

Sponsors

Connecticut Children's Medical Center
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

The investigators will compare the use of exercises augmented with BFR with quantitative measurements of strength and patient reported outcomes. A total of 20 youth and adolescent patients undergoing a surgical procedure for ACL reconstruction at Connecticut Children's Elite Sports Medicine and completing physical therapy at Connecticut Children's Sports Physical Therapy will be recruited for this study. A review of data from 20 previous patients, matched for age, sex, BMI and surgical procedure that completed physical therapy at Connecticut Children's Sports Physical Therapy will be used as a comparison. As part of this pilot study, the investigators will additionally collect prospective controls. This population will be patients not participating in physical therapy at Connecticut Children's but underwent ACL reconstruction by Elite Sports Medicine.

Eligibility

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

Inclusion criteria

* Patients between the age of 12 and 18 years at the time of surgery. * Post-primary ACL reconstruction * Orthopaedic surgical intervention (including all additional procedures at the knee) completed by one of the Elite Sports Medicine physicians. * Patient completed postoperative rehabilitation following standard protocols * No contraindications to performing BFR, as outlined in the Owens Recovery\[18\] Science 2018 Personal Blood Flow Restriction manual.

Exclusion criteria

* Patients older than 18 and younger than 12 at the time of surgery * Any additional diagnoses or deformity not related to knee injury that could affect knee strength * Additional lower extremity injury at time of knee injury (e.g., ankle injury) requiring treatment * Previous surgical intervention on the knee (ipsilateral and contralateral) * Patients with weight bearing restrictions for greater than two weeks after surgery due to concomitant pathology such as meniscal root/radial repair, chondral pathology, or multi-ligament pathology. . Generic exclusion: Subjects not meeting all inclusion criteria.

Design outcomes

Primary

MeasureTime frameDescription
Isometric Quad Strength Peak Torque3 month and return to sport post-operative strength (6-8 months post-op)Isometric strength testing to measure peak torque quadriceps strength (unit: nm/kg) as reported by isokinetic dynamometer on involved and uninvolved limb.
Isometric Quad Strength Limb Symmetry Index3 month and return to sport isometric quad strength limb symmetryQuadriceps limb symmetry index is calculated by taking the values from outcome 1. \[ ( peak torque quadriceps involved limb (nm-kg)/ peak torque quadriceps uninvolved limb (nm-kg))\*100\] as reported by isokinetic dynamometer. This value is expressed as a percentage. 100% would equal perfect symmetry. Should involve limb demonstrate greater strength then uninvolved limb symmetry scores would be greater then 100%
Isometric Hamstring Strength Peak Torqueat 3 months post-op and return to sport (between approximately 6-8 months post-op)Isometric strength testing to measure peak torque hamstring strength (unit:nm/kg) as reported by isokinetic dynamometer on involved and uninvolved limb.
Isometric Hamstring Strength Limb Symmetry Index3 months post op and return to sport (between approximately 6-8 months post-op)Hamstring limb symmetry index is calculated by taking the values from outcome 3 \[ ( peak torque hamstring involved limb (nm-kg) / peak torque hamstring uninvolved limb (nm-kg))\*100\] as reported by isokinetic dynamometer. This value is expressed as a percentage.100% would equal symmetry. For patients that demonstrate a stronger involved limb then uninvolved limb symmetry will be reported as greater then 100%

Secondary

MeasureTime frameDescription
Pedi-IKDC (International Knee Documentation Committee)at 3 months post-op and return to sport (between approximately 6-8 months post-op)Patient 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).

Countries

United States

Participant flow

Participants by arm

ArmCount
BFR Exercise Group
In addition to the standard ACL protocol, patients in this study will utilize the Owen Recovery Science exercise protocol for BFR \[18\]. The following guidelines will be followed concerning exercise progression, occlusion pressure and difficulties with volume achievement. A total of 20 youth and adolescent patients undergoing a surgical procedure for ACL reconstruction at Connecticut Children's Elite Sports Medicine and completing physical therapy at Connecticut Children's Sports Physical Therapy will be recruited for this study. Blood Flow Restriction using Delfi Personalized Tourniquet System: 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 following the Owens Recovery Science Protocol
33
Non-BFR Exercise Group
As part of this pilot study, the investigators will additionally collect prospective controls. This population will be patients not participating in physical therapy at Connecticut Children's but underwent ACL reconstruction by Elite Sports Medicine.
14
Total47

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyLost to Follow-up18
Overall Studymedical/surgical exclusion160

Baseline characteristics

CharacteristicNon-BFR Exercise GroupBFR Exercise GroupTotal
Age, Continuous15.33 years15.46 years15.43 years
Height65.66 inches65.64 inches65.65 inches
Race and Ethnicity Not Collected0 Participants
Sex: Female, Male
Female
9 Participants20 Participants29 Participants
Sex: Female, Male
Male
5 Participants13 Participants18 Participants
weight165 lbs146 lbs151 lbs

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 330 / 14
other
Total, other adverse events
0 / 330 / 14
serious
Total, serious adverse events
0 / 330 / 14

Outcome results

Primary

Isometric Hamstring Strength Limb Symmetry Index

Hamstring limb symmetry index is calculated by taking the values from outcome 3 \[ ( peak torque hamstring involved limb (nm-kg) / peak torque hamstring uninvolved limb (nm-kg))\*100\] as reported by isokinetic dynamometer. This value is expressed as a percentage.100% would equal symmetry. For patients that demonstrate a stronger involved limb then uninvolved limb symmetry will be reported as greater then 100%

Time frame: 3 months post op and return to sport (between approximately 6-8 months post-op)

Population: We enrolled 47 patients in our study. Due to exclusion criteria, patients lost to follow up and COVID-19 pandemic we were unable to use data for all consented patients for both groups.

ArmMeasureGroupValue (MEAN)Dispersion
BFR Exercise GroupIsometric Hamstring Strength Limb Symmetry Index3 months post-op108.32 percentStandard Deviation 21.41
BFR Exercise GroupIsometric Hamstring Strength Limb Symmetry Indexreturn to sport (between approximately 6-8 months post-op)96.74 percentStandard Deviation 11.68
Non-BFR Exercise GroupIsometric Hamstring Strength Limb Symmetry Index3 months post-op80.3 percentStandard Deviation 14.71
Non-BFR Exercise GroupIsometric Hamstring Strength Limb Symmetry Indexreturn to sport (between approximately 6-8 months post-op)85.61 percentStandard Deviation 16.21
Primary

Isometric Hamstring Strength Peak Torque

Isometric strength testing to measure peak torque hamstring strength (unit:nm/kg) as reported by isokinetic dynamometer on involved and uninvolved limb.

Time frame: at 3 months post-op and return to sport (between approximately 6-8 months post-op)

Population: We enrolled 47 patients in our study. Due to exclusion criteria, patients lost to follow up and COVID-19 pandemic we were unable to use all data for consented subjects in both groups.

ArmMeasureGroupValue (MEAN)Dispersion
BFR Exercise GroupIsometric Hamstring Strength Peak Torque3 months post-op1.20 nm/kgStandard Deviation 0.51
BFR Exercise GroupIsometric Hamstring Strength Peak Torquereturn to sport (between approximately 6-8 months post-op)1.53 nm/kgStandard Deviation 0.3
Non-BFR Exercise GroupIsometric Hamstring Strength Peak Torque3 months post-op1.61 nm/kgStandard Deviation 0.36
Non-BFR Exercise GroupIsometric Hamstring Strength Peak Torquereturn to sport (between approximately 6-8 months post-op)1.3 nm/kgStandard Deviation 0.41
Primary

Isometric Quad Strength Limb Symmetry Index

Quadriceps limb symmetry index is calculated by taking the values from outcome 1. \[ ( peak torque quadriceps involved limb (nm-kg)/ peak torque quadriceps uninvolved limb (nm-kg))\*100\] as reported by isokinetic dynamometer. This value is expressed as a percentage. 100% would equal perfect symmetry. Should involve limb demonstrate greater strength then uninvolved limb symmetry scores would be greater then 100%

Time frame: 3 month and return to sport isometric quad strength limb symmetry

Population: We enrolled 47 patients in our study. Due to exclusion criteria, patients lost to follow up and COVID-19 pandemic we were unable to use all patients that were consented for analysis.

ArmMeasureGroupValue (MEAN)Dispersion
BFR Exercise GroupIsometric Quad Strength Limb Symmetry Index3 month post-op68.02 percentStandard Deviation 13.94
BFR Exercise GroupIsometric Quad Strength Limb Symmetry IndexReturn to sport (@ 6-8 months post-op)89.53 percentStandard Deviation 27.74
Non-BFR Exercise GroupIsometric Quad Strength Limb Symmetry Index3 month post-op60.72 percentStandard Deviation 17.54
Non-BFR Exercise GroupIsometric Quad Strength Limb Symmetry IndexReturn to sport (@ 6-8 months post-op)80.97 percentStandard Deviation 10.69
Primary

Isometric Quad Strength Peak Torque

Isometric strength testing to measure peak torque quadriceps strength (unit: nm/kg) as reported by isokinetic dynamometer on involved and uninvolved limb.

Time frame: 3 month and return to sport post-operative strength (6-8 months post-op)

Population: We enrolled 47 patients in our study. Due to exclusion criteria, patients lost to follow up and COVID-19 pandemic we were unable to fully analyze all consented patients in both groups.

ArmMeasureGroupValue (MEAN)Dispersion
BFR Exercise GroupIsometric Quad Strength Peak Torque3 month isometric1.83 Nm/kgStandard Deviation 0.35
BFR Exercise GroupIsometric Quad Strength Peak Torquereturn to sport isometric (between approximately 6-8 months post-op)2.45 Nm/kgStandard Deviation 0.64
Non-BFR Exercise GroupIsometric Quad Strength Peak Torque3 month isometric1.31 Nm/kgStandard Deviation 0.63
Non-BFR Exercise GroupIsometric Quad Strength Peak Torquereturn to sport isometric (between approximately 6-8 months post-op)2.1 Nm/kgStandard Deviation 0.6
Secondary

Pedi-IKDC (International Knee Documentation Committee)

Patient 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).

Time frame: at 3 months post-op and return to sport (between approximately 6-8 months post-op)

Population: We enrolled 47 patients in our study. Due to exclusion criteria, patients lost to follow up and COVID-19 pandemic we were unable to use all data for all consented patients in both groups

ArmMeasureGroupValue (MEAN)Dispersion
BFR Exercise GroupPedi-IKDC (International Knee Documentation Committee)3 months68.91 units on a scaleStandard Deviation 9.68
BFR Exercise GroupPedi-IKDC (International Knee Documentation Committee)return to sport (between approximately 6-8 months post-op)89.42 units on a scaleStandard Deviation 7.94
Non-BFR Exercise GroupPedi-IKDC (International Knee Documentation Committee)3 months71.82 units on a scaleStandard Deviation 16.78
Non-BFR Exercise GroupPedi-IKDC (International Knee Documentation Committee)return to sport (between approximately 6-8 months post-op)80.90 units on a scaleStandard Deviation 8.04

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