Effectiveness of Blood Flow Restriction Exercise Therapy to Reduce Pain in Knee Osteoarthritis Patients (BFR;OA)
Primary Purpose
Knee Osteoarthritis
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Blood Flow Restriction (BFR)
Sham Blood Flow Restriction (sham BFR)
Sponsored by
About this trial
This is an interventional treatment trial for Knee Osteoarthritis focused on measuring chronic pain
Eligibility Criteria
Inclusion Criteria:
- Current osteoarthritis clinical diagnosis according to either European League Against Rheumatism (EULAR) or American College of Rheumatology (ACR) criteria
- VAS/NRS Knee pain ≥3/10 during activity
Exclusion Criteria:
- Previous experience with BFR
- Has followed knee exercise or kinesiotherapy program in the past 3 months
- New medicines in the past 3 months
- Any lower limb surgery in the past 6 months
- Knee arthroplasty surgery (Knee replacement)
- Any active healing process affecting walking (fracture, sprain, strain, etc.)
- Diagnosed with rheumatologic/neurologic disease affecting functionality
- Diagnosed or history of heart or vascular diseases
- Diagnosed with respiratory/metabolic disease
- Personal history of cancer
- Cognitive problems
- Pregnancy (only for female participants)
- Any other indication not to participate in exercise
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
BFR group
Sham BFR group
Arm Description
The intervention group will receive resisted knee extension 30% of 1RM with blood flow restriction.
The control group will receive resisted knee extension 30% of 1RM with sham blood flow restriction.
Outcomes
Primary Outcome Measures
Change of Pain Pressure Threshold (PPT) from baseline
Pain will be measured with a digital dynamometer. Raise of the PPT value means a better outcome
Secondary Outcome Measures
Change of Dynamic weight-bearing Assessment of Pain (DAP) from baseline
DAP is correlating VAS/NRS pain reporting scales with the functional test of 30-second Chair Stand Test (30s-CST)
Change of 30-second Chair Stand Test (30s-CST) from baseline
30s-CST is a functional assessment evaluating leg strength and dynamic balance, the more repetitions one can do during the 30'', the better the outcome
Change of pain score from baseline with the use of reporting scales Visual Analogue Scale (VAS) / Numeric Rating Scale (NRS)
Pain reporting scales as NRS are using 0-10 grades to measure how big the pain is, 10 is for the worst pain
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04917952
Brief Title
Effectiveness of Blood Flow Restriction Exercise Therapy to Reduce Pain in Knee Osteoarthritis Patients
Acronym
BFR;OA
Official Title
Effectiveness of Blood Flow Restriction (BFR) Exercise Therapy to Reduce Pain in Knee Osteoarthritis (OA) Patients. A Double-blinded Randomised Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
June 2021
Overall Recruitment Status
Unknown status
Study Start Date
June 2021 (Anticipated)
Primary Completion Date
August 2021 (Anticipated)
Study Completion Date
August 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of West Attica
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.
Yes
Data Monitoring Committee
No
5. Study Description
Brief Summary
Resistance training of knee extensor muscles is being used in physiotherapy management in knee osteoarthritis (OA) to improve pain and physical function. Blood flow restriction (BFR) has been suggested to improve pain and increase muscle strength in healthy subjects and certain diseases. Although there are clinical studies suggesting improvements in knee osteoarthritis symptoms after 4-12 weeks of exercise with BFR, the acute effects of the intervention have not been known.
This study aims to assess the effectiveness of low load exercise therapy combined with BFR on acute pain reduction and within 24 hours post-intervention on people with knee OA compared to a placebo group.
This study will take place in Athens, Greece, as part of the postgraduate MSc program of the Physiotherapy department of the University of West Attica.
Detailed Description
A double-blinded randomised clinical trial with a total of 42 participants will be randomly assigned to the intervention (n=21) or the control group (n=21).
The intervention group will complete a single exercise session with BFR 80%, 30% 1RM, while the control group will have sham BFR, 30% 1RM.
Pain Pressure Threshold (PPT) will be assessed with the use of a digital pressure dynamometer.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Knee Osteoarthritis
Keywords
chronic pain
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
42 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
BFR group
Arm Type
Experimental
Arm Description
The intervention group will receive resisted knee extension 30% of 1RM with blood flow restriction.
Arm Title
Sham BFR group
Arm Type
Placebo Comparator
Arm Description
The control group will receive resisted knee extension 30% of 1RM with sham blood flow restriction.
Intervention Type
Device
Intervention Name(s)
Blood Flow Restriction (BFR)
Other Intervention Name(s)
Kaatsu
Intervention Description
Exercise: Bilateral knee extension at range 90ο-0ο
Load: 30% 1RM
BFR: Yes, 80% at both legs
Sets: 4
Reps: 30-15-15-15
Rest: 30'' between sets
Tempo: 2-0-2-0
Participants of the intervention group will receive an exercise protocol with blood flow restriction once and will be measured for changes in PPT by the use of a digital dynamometer.
Exercise protocol will be four sets of bilateral knee extension 90ο-0ο, reps per set 30-15-15-15, tempo 2-0-2-0 and rest 30 sec between sets.
In order to determine the training load 30% of 1RM, participants will perform bilateral knee extension in range 90ο-0ο with pain-free maximum resistance. The derived 1RM will be used to determine the 30% 1RM load.
Blood flow restriction will be applied at 80% by using pressure cuffs. The cuffs will be applied to the proximal thigh. Cuff pressure needed for a 100% vascular occlusion will be determined for each individual at a seated and relaxed position.
Intervention Type
Device
Intervention Name(s)
Sham Blood Flow Restriction (sham BFR)
Other Intervention Name(s)
Sham Kaatsu
Intervention Description
Exercise: Bilateral knee extension at range 90ο-0ο
Load: 30% 1RM
BFR: Yes, Sham BFR, 10mm Hg at both legs
Sets: 4
Reps: 30-15-15-15
Rest: 30'' between sets
Tempo: 2-0-2-0
Participants of the control group will receive an exercise protocol with sham blood flow restriction once and will be measured for changes in PPT by the use of a digital dynamometer.
Exercise protocol will be four sets of bilateral knee extension 90ο-0ο, reps per set 30-15-15-15, tempo 2-0-2-0 and rest 30 sec between sets.
In order to determine the training load 30% of 1RM, participants will perform bilateral knee extension in range 90ο-0ο with pain-free maximum resistance. The derived 1RM will be used to determine the 30% 1RM load.
Sham technique for blood flow restriction will be applied by using pressure cuffs inflated at 10mm Hg. The cuffs will be applied to the proximal thigh. Cuff pressure will be applied for each individual at a seated and relaxed position.
Primary Outcome Measure Information:
Title
Change of Pain Pressure Threshold (PPT) from baseline
Description
Pain will be measured with a digital dynamometer. Raise of the PPT value means a better outcome
Time Frame
At baseline, Post 5 minutes, Post 24 hours
Secondary Outcome Measure Information:
Title
Change of Dynamic weight-bearing Assessment of Pain (DAP) from baseline
Description
DAP is correlating VAS/NRS pain reporting scales with the functional test of 30-second Chair Stand Test (30s-CST)
Time Frame
At baseline, Post 5 minutes, Post 24 hours
Title
Change of 30-second Chair Stand Test (30s-CST) from baseline
Description
30s-CST is a functional assessment evaluating leg strength and dynamic balance, the more repetitions one can do during the 30'', the better the outcome
Time Frame
At baseline, Post 5 minutes, Post 24 hours
Title
Change of pain score from baseline with the use of reporting scales Visual Analogue Scale (VAS) / Numeric Rating Scale (NRS)
Description
Pain reporting scales as NRS are using 0-10 grades to measure how big the pain is, 10 is for the worst pain
Time Frame
At baseline, Post 5 minutes, Post 24 hours
Other Pre-specified Outcome Measures:
Title
Douleur Neuropathique 4 questionnaire (DN4 greek)
Description
Greek version of DN4 will be used diagnostically to identify the existence of neuropathic pain, a score greater than 4/10 suggests the existence of neuropathic pain
Time Frame
At least 72 hours prior the intervention
Title
Knee Osteoarthritis Outcome Scale (KOOS greek)
Description
Greek version of the KOOS will be used diagnostically to identify the severity of the disease. Each category score ranges 0-100, the minimum score is the worst
Time Frame
At least 72 hours prior the intervention
Title
1 Repetition Maximum (1RM)
Description
1RM will be used diagnostically to identify the maximum strength of the participants. Each participant will extend their knees bilaterally, pain-free, 90o-0ο with the maximum weight
Time Frame
At least 72 hours prior the intervention
Title
Other demographics and medical notes
Description
Recording of demographics and medical notes will be used to identify the inclusion and exclusion criteria
Time Frame
At least 72 hours prior the intervention
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Current osteoarthritis clinical diagnosis according to either European League Against Rheumatism (EULAR) or American College of Rheumatology (ACR) criteria
VAS/NRS Knee pain ≥3/10 during activity
Exclusion Criteria:
Previous experience with BFR
Has followed knee exercise or kinesiotherapy program in the past 3 months
New medicines in the past 3 months
Any lower limb surgery in the past 6 months
Knee arthroplasty surgery (Knee replacement)
Any active healing process affecting walking (fracture, sprain, strain, etc.)
Diagnosed with rheumatologic/neurologic disease affecting functionality
Diagnosed or history of heart or vascular diseases
Diagnosed with respiratory/metabolic disease
Personal history of cancer
Cognitive problems
Pregnancy (only for female participants)
Any other indication not to participate in exercise
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Christos D. Anagnostis
Phone
+306909921606
Email
mscphys18003@uniwa.gr
First Name & Middle Initial & Last Name or Official Title & Degree
George Gioftsos
Phone
+302105387485
Email
gioftsos@uniwa.gr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
George Gioftsos
Organizational Affiliation
University of West Attica
Official's Role
Study Director
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Effectiveness of Blood Flow Restriction Exercise Therapy to Reduce Pain in Knee Osteoarthritis Patients
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