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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
University of West Attica
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Knee Osteoarthritis focused on measuring chronic pain

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

    First Posted
    May 25, 2021
    Last Updated
    June 1, 2021
    Sponsor
    University of West Attica
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    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

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    Effectiveness of Blood Flow Restriction Exercise Therapy to Reduce Pain in Knee Osteoarthritis Patients

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