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ACL Bone Health and Loading Study (ACLBONE)

Primary Purpose

ACL Tear

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Delfi's PTS Personalized Tourniquet System for Blood Flow Restriction Group
Standard ACL rehab
Sponsored by
Bryan Bourcier
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for ACL Tear focused on measuring Blood Flow Restriction (BFR)

Eligibility Criteria

16 Years - 22 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Athletes undergoing ACL reconstruction with or without meniscal pathology
  • MRI confirming ACL tear
  • Athletes ages 16-22

Exclusion Criteria:

  • Any Cognitively impaired athletes
  • Athletes not in age range of 16-22
  • Athletes who have additional ligament repair or chondral repair.
  • Athletes with any weight bearing restrictions greater than 4 weeks.
  • Athletes with re-tears or history of contralateral ACL tears
  • Athletes with any systemic neuromuscular or balance disorders will not be allowed
  • Athletes who do not or are unable to provide consent or assent (with Parental consent).
  • Pregnant women will be excluded.
  • Athlete who has previously used Blood Flow Restriction
  • Athletes who are unable or unwilling to complete all rehabilitation with Parkview Athletic Rehab at SportONE Parkview Fieldhouse

Sites / Locations

  • Parkview Athletic RehabRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Delfi's PTS Personalized Tourniquet System for Blood Flow Restriction Group

Non Delfi PTS Personalized Tourniquet System for Blood Flow Restriction Group

Arm Description

This group will use Delfi's PTS Personalized Tourniquet System for Blood Flow Restriction for rehab.

Standard post operative ACL rehab without Blood flow restriction

Outcomes

Primary Outcome Measures

Leg Weight distribution landing on force plates
Athlete landing on force plates from and 18 inch height to compare loading / weight symmetry

Secondary Outcome Measures

Bone mineral density
Bone mineral density of distal femur and proximal tibia

Full Information

First Posted
December 8, 2020
Last Updated
September 5, 2023
Sponsor
Bryan Bourcier
Collaborators
Parkview Health
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1. Study Identification

Unique Protocol Identification Number
NCT04682392
Brief Title
ACL Bone Health and Loading Study
Acronym
ACLBONE
Official Title
The Effects of Bone Health on Landing Mechanics on Patients Post ACL Reconstruction.
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 17, 2021 (Actual)
Primary Completion Date
January 1, 2025 (Anticipated)
Study Completion Date
January 1, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Bryan Bourcier
Collaborators
Parkview Health

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to look at the effects of bone density on lower extremity loading mechanics using Blood Flow Restriction (BFR) to provide the control group for bone health. Hypothesis: The BFR group will have decreased bone mineral loss and improved functional performance compared to control group.
Detailed Description
Group 1 - ACL without BFR : 30 athletes with ACL tears and will NOT do blood flow restriction (BFR). Random group allocation will be determined using envelopes for allocation concealment. The control group will be tested with a Dexascan immediately post appointment confirming MRI findings of ACL tear and scheduling surgery. They will be then Scanned again at first therapy appointment within 24-48 hours of surgery. Then Dexascans will be done every 4 weeks until 28 weeks with a maximum of 9 scans. The scans will be completed on a normally scheduled rehabilitation session at the convenience of the radiology techs availability. The investigators will collect force plate measurements for squat symmetry at first 4-week assessment period, and then for landing symmetry every 4 weeks after that until 28 weeks. Group 2 - ACL with BFR: 30 athletes with ACL tear that will receive BFR. This group will be selected in the same manner as the control group. They will be tested with a dexasan immediately post appointment confirming MRI findings of ACL tear and scheduling surgery. At the initial dexascan they will also be instructed in Blood flow restriction and do exercises with blood flow restriction to prepare for initial post-surgical visit. They will be then scanned again at first therapy appointment within 24-48 hours of surgery. Then Dexascans will be done every 4 weeks until 28 weeks with a maximum of 9 scans. The investigators will collect force plate measurements for squat symmetry at first 4-week assessment and then for landing symmetry every 4 weeks after that until 28 weeks. The standard of care following ACL tear does not include Dexascan, force plate measurements, or blood flow restriction. Independent Variable 1. Blood Flow Restrictions (BFR) Dependent Variable Landing mechanics / force distribution Bone Mineral Density /Bone mass Lean Muscle Mass (LM) Pain via Visual Analogue Scale (VAS) Quad Strength using microFET®2 Digital Handheld Dynamometer Hamstring strength using microFET®2 Digital Handheld Dynamometer SL Hop Distance Triple Hop Distance Crossover hop Distance Keiser leg press max power at 5 reps at body weight Procedures: Once a participant has been identified as meeting the inclusion criteria with a positive MRI finding and have agreed to schedule surgery, they will be allocated to either the control or experimental group. Random group allocation will be determined using envelopes for allocation concealment. Prior to initiation of the study, a research assistant not involved in data collection will use a random number generator to create the randomization sequence allocating an equal number of participants to each of the 2 groups, the control non BFR group and the experimental BFR group. The randomization will be concealed by having the group assignment placed inside a sealed opaque envelope within potential participant folders. This process will be documented and signed by the randomizer. Once selected and enrolled, the group assignment will be revealed and will not be blinded to either the participant or the researchers. The pre-op therapy session will be completed 48-72 hours following MRI confirmation of ACL tear if they have opted for surgical intervention. The initial post-op therapy session will be completed within 24-48 hours of surgery. All participants will undergo bone mineral density (BMD), bone mass, and lean muscle mass (LM) measurements using Dexascan at pre-op visit, and again at initial post op visit ad then every 4 weeks from week 4-16. Participants will also complete a total of 9 landing/jumping trials as part of testing, with rest as needed. Following the warm-up, subjects will complete 3 drop landings, 3 drop vertical jumps, and 3 countermovement jumps. The participant must demonstrate safe landing mechanics on the drop landings as determined by testing PT in order to attempt the drop vertical jumps and the countermovement jumps. Landing assessment will be collected at initial landing session at weeks 8, 12,16,20, 24, and 28 weeks post op. The exercises selection and progression will be standardized for BFR intervention across all subjects. The BFR group will exercise with 80% arterial limb occlusion using the Delphi automated tourniquet around the proximal thigh outfitted with Doppler (Delfi®). If 80% arterial limb occlusion is not tolerated by the participant, the pressure will be decreased to tolerance. However, the pressure will not be lowered below 60% as there is a floor effect at 60% LOP where BFR is no longer beneficial. Exercises will be performed for 4 sets of 30-15-15-15 repetitions separated by 30s of rest and 1 BFR exercise will be performed. SL hop, Triple hop, Crossover hop, and Keiser leg press power will be measured at 12, 16, 20 and 24 weeks. Strength testing will be done with microFET®2 Digital Handheld Dynamometer every 2 weeks of the rehab process in accordance with standard rehab protocol.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
ACL Tear
Keywords
Blood Flow Restriction (BFR)

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
2 groups with Randomized group assignments
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Delfi's PTS Personalized Tourniquet System for Blood Flow Restriction Group
Arm Type
Active Comparator
Arm Description
This group will use Delfi's PTS Personalized Tourniquet System for Blood Flow Restriction for rehab.
Arm Title
Non Delfi PTS Personalized Tourniquet System for Blood Flow Restriction Group
Arm Type
Active Comparator
Arm Description
Standard post operative ACL rehab without Blood flow restriction
Intervention Type
Device
Intervention Name(s)
Delfi's PTS Personalized Tourniquet System for Blood Flow Restriction Group
Other Intervention Name(s)
A Dephi Personal Tourniquet System will be utilized for the experimental group.
Intervention Description
A Delphi Personal Tourniquet system for blood flow restriction (BFR) therapy will be applied to each treatment session for this group. They will do 3-5 exercises with the BFR system on the surgical or both lower extremities for bilateral or unilateral movements.
Intervention Type
Other
Intervention Name(s)
Standard ACL rehab
Intervention Description
Standard accelerated ACL protocol
Primary Outcome Measure Information:
Title
Leg Weight distribution landing on force plates
Description
Athlete landing on force plates from and 18 inch height to compare loading / weight symmetry
Time Frame
week 28 post surgery
Secondary Outcome Measure Information:
Title
Bone mineral density
Description
Bone mineral density of distal femur and proximal tibia
Time Frame
Week 28 post surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
22 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Athletes undergoing ACL reconstruction with or without meniscal pathology MRI confirming ACL tear Athletes ages 16-22 Exclusion Criteria: Any Cognitively impaired athletes Athletes not in age range of 16-22 Athletes who have additional ligament repair or chondral repair. Athletes with any weight bearing restrictions greater than 4 weeks. Athletes with re-tears or history of contralateral ACL tears Athletes with any systemic neuromuscular or balance disorders will not be allowed Athletes who do not or are unable to provide consent or assent (with Parental consent). Pregnant women will be excluded. Athlete who has previously used Blood Flow Restriction Athletes who are unable or unwilling to complete all rehabilitation with Parkview Athletic Rehab at SportONE Parkview Fieldhouse
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Bryan T Bourcier, DPT
Phone
2607402518
Email
bryan.bourcier@parkview.com
First Name & Middle Initial & Last Name or Official Title & Degree
Thomas M Ruediger, DPT
Phone
8106181897
Email
thomas.ruediger@parkview.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bryan T Bourcier, DPT
Organizational Affiliation
Parkview Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
Parkview Athletic Rehab
City
Fort Wayne
State/Province
Indiana
ZIP/Postal Code
46805
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bryan T Bourcier, DPT
Phone
260-740-2518
Email
bryan.bourcier@parkview.com
First Name & Middle Initial & Last Name & Degree
Ryan Nelson, DPT
Phone
7657497019
Email
ryan.nelson@parkview.com
First Name & Middle Initial & Last Name & Degree
Jonathan Dettmer, DPT
First Name & Middle Initial & Last Name & Degree
Thomas Ruediger, DPT

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
20810081
Citation
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Results Reference
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PubMed Identifier
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Citation
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ACL Bone Health and Loading Study

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