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Blood Flow Restriction to Improve Muscle Strength After ACL Injury

Primary Purpose

Anterior Cruciate Ligament Injury

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
DELFI PTS Personalized Tourniquet System for Blood Flow Restriction Training
Eccentric Exercise with BLAST Leg Press System
Concentric Exercise with BLAST Leg Press System
Sponsored by
University of Michigan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anterior Cruciate Ligament Injury focused on measuring ACL, Knee, Muscle

Eligibility Criteria

14 Years - 30 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. suffered an acute, complete ACL rupture as confirmed by MRI
  2. scheduled to undergo ACL reconstruction
  3. scheduled to undergo ACL reconstruction with a surgeon affiliated with MedSport (University of Michigan Orthopaedic Clinic)
  4. willing to undergo rehabilitation through MedSport (University of Michigan Orthopaedic Clinic) 5)) Willingness to participate in testing and follow-up as outlined in the protocol

6) English-speaking

Exclusion Criteria:

  1. inability to provide written informed consent (or assent)
  2. female subjects who are pregnant or are planning to become pregnant during the study timeframe
  3. previous ACL injury
  4. previous surgery to either knee
  5. bony fracture accompanying ACL injury
  6. chronic ACL injuries (for our study, this is defined as patient reporting to a physician greater than 2 weeks after initial injury)
  7. patients who experienced a knee dislocation
  8. History of blood clots
  9. Previous deep vein thrombosis
  10. Use of estrogen or progestin contraceptive
  11. History of cerebrovascular disease
  12. History of peripheral vascular disease
  13. History of Sickle Cell Anemia
  14. History of chronic muscular disorder (e.g. fibromyalgia)
  15. History of severe hypertension

Sites / Locations

  • University of Michigan

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Active Comparator

Active Comparator

Arm Label

Eccentric Exercise with Delfi Blood Flow Restriction Training

Concentric Exercise with Delfi Blood Flow Restriction Training

Eccentric Exercise

Concentric Exercise

Arm Description

Patients randomized to the eccentric exercise + blood flow restriction training group will receive eccentric exercise two times per week for 8 weeks, beginning 8-12 weeks after anterior cruciate ligament reconstruction. Patients will completed the exercise with knee range of motion limited to 20-60 degrees of knee flexion and will train at an intensity equal to 70% of their eccentric 1-repetition maximum for 4 sets of 10 repetitions. During exercise, patients will have the DELFI personalized tourniquet system applied over the quadriceps to restrict blood flow. The tourniquet will be set to a limb occlusion pressure of 80%.

Patients randomized to the concentric exercise group will receive concentric exercise two times per week for 8 weeks, beginning 8-12 weeks after anterior cruciate ligament reconstruction. Patients will completed the exercise with knee range of motion limited to 20-60 degrees of knee flexion and will train at an intensity equal to 70% of their concentric 1-repetition maximum for 4 sets of 10 repetitions.

Patients randomized to the eccentric exercise group will receive eccentric exercise two times per week for 8 weeks, beginning 8-12 weeks after anterior cruciate ligament reconstruction. Patients will completed the exercise with knee range of motion limited to 20-60 degrees of knee flexion and will train at an intensity equal to 70% of their eccentric 1-repetition maximum for 4 sets of 10 repetitions.

Patients randomized to the concentric exercise group will receive concentric exercise two times per week for 8 weeks, beginning 8-12 weeks after anterior cruciate ligament reconstruction. Patients will completed the exercise with knee range of motion limited to 20-60 degrees of knee flexion and will train at an intensity equal to 70% of their concentric 1-repetition maximum for 4 sets of 10 repetitions. During exercise, patients will have the DELFI personalized tourniquet system applied over the quadriceps to restrict blood flow. The tourniquet will be set to a limb occlusion pressure of 80%.

Outcomes

Primary Outcome Measures

Change from baseline to return to activity in quadriceps muscle strength
concentric isokinetic muscle strength at 60 degrees per second

Secondary Outcome Measures

Knee Flexion Angle
Peak knee flexion angle recorded during a single-legged hop (units: degrees)
Knee Flexion Moment
Peak knee flexion moment recorded during a single-legged hop (units: Nm/kg)
Change from baseline to pre-intervention in PROMIS Global Health Scale
Patient-reported outcome measured to assess health related quality of life. Physical Function Average: t score = 50±10 Min: 10 Max: 90
Change from baseline to post-intervention in PROMIS Global Health Scale
Patient-reported outcome measured to assess health related quality of life. Physical Function Average: t score = 50±10 Min: 10 Max: 90
Change from baseline to return to activity in PROMIS Global Health Scale
Patient-reported outcome measured to assess health related quality of life. Physical Function Average: t score = 50±10 Min: 10 Max: 90

Full Information

First Posted
April 17, 2017
Last Updated
January 19, 2019
Sponsor
University of Michigan
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1. Study Identification

Unique Protocol Identification Number
NCT03141801
Brief Title
Blood Flow Restriction to Improve Muscle Strength After ACL Injury
Official Title
Blood Flow Restriction Training to Improve Muscle Strength and Function Following Anterior Cruciate Ligament Injury
Study Type
Interventional

2. Study Status

Record Verification Date
January 2019
Overall Recruitment Status
Completed
Study Start Date
August 25, 2016 (Actual)
Primary Completion Date
November 21, 2018 (Actual)
Study Completion Date
November 21, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Michigan

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Quadriceps muscle weakness is a common consequence following anterior cruciate ligament (ACL) injury and reconstruction. Maximizing quadriceps strength following ACL injury is significant as diminished quadriceps strength has been linked to the osteoarthritis that affects over 50% of surgically reconstructed limbs. Given that knee joint health following ACL injury is predicated on restoring quadriceps strength, identifying treatment approaches capable of improving strength is paramount. Blood flow restriction training (BFRT) is a method where oxygen to the muscle is intentionally reduced during exercise/rehabilitation and may lead to more timely and substantial strength gains. In the proposed project, we will examine the efficacy of BFRT in patients who have undergone ACL reconstruction and suffer from substantial quadriceps weakness.
Detailed Description
Quadriceps muscle weakness is a common consequence following anterior cruciate ligament (ACL) injury and reconstruction. Maximizing quadriceps strength following ACL injury is significant as diminished quadriceps strength has been linked to the osteoarthritis that affects over 50% of surgically reconstructed limbs. Given that knee joint health following ACL injury is predicated on restoring quadriceps strength, identifying treatment approaches capable of improving strength is paramount. Blood flow restriction training (BFRT) is a method whereby oxygen to the muscle is intentionally reduced during exercise/rehabilitation and may lead to more timely and substantial strength gains. In the proposed project, we will examine the efficacy of BFRT in patients who have undergone ACL reconstruction and suffer from quadriceps weakness. This project will have a randomized clinical trial design. Sixty patients that have torn their ACL and plan to undergo surgical reconstruction will be randomized into one of four groups: 1) eccentric exercise; 2) concentric exercise; 3) eccentric exercise with blood flow restriction; or 4) concentric exercise with blood flow restriction. All patients regardless of randomization assignment will also receive standard of care ACL rehabilitation. Approximately 6 weeks after ACL reconstruction surgery, patients will begin to receive the study interventions which will last for 8 weeks. The concentric exercise will be a leg press exercise done on a conventional leg press machine, while the eccentric exercise will be a leg press exercise done on a device designed to elicit eccentric muscle contractions. Patients will train at 70% of their 1 repetition maximum and will complete 4 sets of 10 contractions at each session (2 sessions/week). For patients randomized to the BFRT groups they will complete the leg press exercise while blood flow the the quadriceps muscle is restricted with a BFRT device (Delfi Personalized Tourniquet System for Blood Flow Restriction). We will quantify our dependent variables prior to surgical reconstruction, 6 weeks post-operatively (before study intervention starts), 14 weeks post-operatively (immediately after study intervention ends), and time of physician discharge from rehabilitation (e.g. time medical clearance for return to activity). The primary outcome is isokinetic quadriceps strength. We hypothesize that patients who complete eccentric exercise along with blood flow restriction training will realize the greatest gains in muscle strength. The DELFI PTS Personalized Tourniquet system is exempt from premarket notification and is therefore not subject to 510(k)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anterior Cruciate Ligament Injury
Keywords
ACL, Knee, Muscle

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
48 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Eccentric Exercise with Delfi Blood Flow Restriction Training
Arm Type
Experimental
Arm Description
Patients randomized to the eccentric exercise + blood flow restriction training group will receive eccentric exercise two times per week for 8 weeks, beginning 8-12 weeks after anterior cruciate ligament reconstruction. Patients will completed the exercise with knee range of motion limited to 20-60 degrees of knee flexion and will train at an intensity equal to 70% of their eccentric 1-repetition maximum for 4 sets of 10 repetitions. During exercise, patients will have the DELFI personalized tourniquet system applied over the quadriceps to restrict blood flow. The tourniquet will be set to a limb occlusion pressure of 80%.
Arm Title
Concentric Exercise with Delfi Blood Flow Restriction Training
Arm Type
Experimental
Arm Description
Patients randomized to the concentric exercise group will receive concentric exercise two times per week for 8 weeks, beginning 8-12 weeks after anterior cruciate ligament reconstruction. Patients will completed the exercise with knee range of motion limited to 20-60 degrees of knee flexion and will train at an intensity equal to 70% of their concentric 1-repetition maximum for 4 sets of 10 repetitions.
Arm Title
Eccentric Exercise
Arm Type
Active Comparator
Arm Description
Patients randomized to the eccentric exercise group will receive eccentric exercise two times per week for 8 weeks, beginning 8-12 weeks after anterior cruciate ligament reconstruction. Patients will completed the exercise with knee range of motion limited to 20-60 degrees of knee flexion and will train at an intensity equal to 70% of their eccentric 1-repetition maximum for 4 sets of 10 repetitions.
Arm Title
Concentric Exercise
Arm Type
Active Comparator
Arm Description
Patients randomized to the concentric exercise group will receive concentric exercise two times per week for 8 weeks, beginning 8-12 weeks after anterior cruciate ligament reconstruction. Patients will completed the exercise with knee range of motion limited to 20-60 degrees of knee flexion and will train at an intensity equal to 70% of their concentric 1-repetition maximum for 4 sets of 10 repetitions. During exercise, patients will have the DELFI personalized tourniquet system applied over the quadriceps to restrict blood flow. The tourniquet will be set to a limb occlusion pressure of 80%.
Intervention Type
Device
Intervention Name(s)
DELFI PTS Personalized Tourniquet System for Blood Flow Restriction Training
Other Intervention Name(s)
Kaatsu Training
Intervention Description
cuff is inflated to 80% of an individuals limb occlusion pressure
Intervention Type
Other
Intervention Name(s)
Eccentric Exercise with BLAST Leg Press System
Intervention Description
4 sets of 10 repetitions of an eccentric leg press exercise performed at 70% of the 1 repetition maximum
Intervention Type
Other
Intervention Name(s)
Concentric Exercise with BLAST Leg Press System
Intervention Description
4 sets of 10 repetitions of an concentric leg press exercise performed at 70% of the 1 repetition maximum
Primary Outcome Measure Information:
Title
Change from baseline to return to activity in quadriceps muscle strength
Description
concentric isokinetic muscle strength at 60 degrees per second
Time Frame
Pre-surgery (baseline), Return to Activity (~9 months post-surgery)
Secondary Outcome Measure Information:
Title
Knee Flexion Angle
Description
Peak knee flexion angle recorded during a single-legged hop (units: degrees)
Time Frame
Return to Activity (~9 months post-surgery)
Title
Knee Flexion Moment
Description
Peak knee flexion moment recorded during a single-legged hop (units: Nm/kg)
Time Frame
Return to Activity (~9 months post-surgery)
Title
Change from baseline to pre-intervention in PROMIS Global Health Scale
Description
Patient-reported outcome measured to assess health related quality of life. Physical Function Average: t score = 50±10 Min: 10 Max: 90
Time Frame
Pre-surgery (baseline), Pre-intervention (~10 weeks post-surgery)
Title
Change from baseline to post-intervention in PROMIS Global Health Scale
Description
Patient-reported outcome measured to assess health related quality of life. Physical Function Average: t score = 50±10 Min: 10 Max: 90
Time Frame
Pre-surgery (baseline), Post-intervention (~18 weeks post-surgery)
Title
Change from baseline to return to activity in PROMIS Global Health Scale
Description
Patient-reported outcome measured to assess health related quality of life. Physical Function Average: t score = 50±10 Min: 10 Max: 90
Time Frame
Pre-surgery (baseline),Return to Activity (~9 months post-surgery)
Other Pre-specified Outcome Measures:
Title
Change from baseline to pre-intervention in quadriceps cross-sectional area
Description
cross-sectional area of the quadriceps muscle
Time Frame
Pre-surgery (baseline), Pre-intervention (~10 weeks post-surgery)
Title
Change from baseline to post-intervention in quadriceps cross-sectional area
Description
cross-sectional area of the quadriceps muscle
Time Frame
Pre-surgery (baseline), Post-intervention (~18 weeks post-surgery)
Title
Change from baseline to return to activity in quadriceps cross-sectional area
Description
cross-sectional area of the quadriceps muscle
Time Frame
Pre-surgery (baseline), Return to Activity (~9 months post-surgery)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
14 Years
Maximum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: suffered an acute, complete ACL rupture as confirmed by MRI scheduled to undergo ACL reconstruction scheduled to undergo ACL reconstruction with a surgeon affiliated with MedSport (University of Michigan Orthopaedic Clinic) willing to undergo rehabilitation through MedSport (University of Michigan Orthopaedic Clinic) 5)) Willingness to participate in testing and follow-up as outlined in the protocol 6) English-speaking Exclusion Criteria: inability to provide written informed consent (or assent) female subjects who are pregnant or are planning to become pregnant during the study timeframe previous ACL injury previous surgery to either knee bony fracture accompanying ACL injury chronic ACL injuries (for our study, this is defined as patient reporting to a physician greater than 2 weeks after initial injury) patients who experienced a knee dislocation History of blood clots Previous deep vein thrombosis Use of estrogen or progestin contraceptive History of cerebrovascular disease History of peripheral vascular disease History of Sickle Cell Anemia History of chronic muscular disorder (e.g. fibromyalgia) History of severe hypertension
Facility Information:
Facility Name
University of Michigan
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
32167837
Citation
Curran MT, Bedi A, Mendias CL, Wojtys EM, Kujawa MV, Palmieri-Smith RM. Blood Flow Restriction Training Applied With High-Intensity Exercise Does Not Improve Quadriceps Muscle Function After Anterior Cruciate Ligament Reconstruction: A Randomized Controlled Trial. Am J Sports Med. 2020 Mar;48(4):825-837. doi: 10.1177/0363546520904008.
Results Reference
derived

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Blood Flow Restriction to Improve Muscle Strength After ACL Injury

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