Effects of Low-Load Blood Flow Restriction Resistance Training With and Without Hip Abductor Strengthening in Patients With Knee Osteoarthritis.(BFR)
yes
1 other identifier
interventional
44
1 country
1
Brief Summary
This study aims to compare the effects of low-load Blood Flow Restriction (BFR) resistance training with and without hip abductor strengthening in patients with knee osteoarthritis. It will evaluate the effectiveness of both treatment approaches in reducing knee pain, improving range of motion, increasing muscle strength, and enhancing functional ability. The study will determine which intervention provides better clinical outcomes in patients with knee osteoarthritis.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable knee-osteoarthritis
Started Oct 2026
Shorter than P25 for not_applicable knee-osteoarthritis
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
October 17, 2026
CompletedStudy Start
First participant enrolled
October 20, 2026
CompletedFirst Posted
Study publicly available on registry
October 23, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2026
October 23, 2026
October 1, 2026
2 months
October 17, 2026
October 17, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Numeric Pain Rating Scale NRPS
11-point numeric with 0 representing No pain, 1-3 representing Mild Pain (nagging, annoying, interfering little with ADLs), 4-6 representing Moderate Pains (interferes significantly with ADLs), 7-10 representing Sever Pain
Baseline and post treatment after 6 weeks
Western Ontario And McMasters Universities Osteoarthritis Index (WOMAC)
The WOMAC is a disease-specific questionnaire designed to assess symptoms and functional limitations in individuals with knee and hip osteoarthritis. It consists of 24 items divided into three domains: Pain (5 items), Stiffness (2 items), and Physical.Function (1 7 items). The WOMAC is widely used to evaluate the impact of osteoarthritis on daily activities and quality of life.Higher WOMAC scores indicate greater pain, stiffness, and functional disability, whereas lower scores represent betterfunctional status and symptom improvement.
Baseline and post treatment after 6 weeks
Goniometer
A goniometer is a reliable clinical tool used to measure knee flexion and extension ROM in patients with knee osteoarthritis, assess joint mobility, monitor disease progression, and evaluate rehabilitation outcomes. Normal knee flexion is approximately 135°-140° and extension is 0°. Reduced ROM indicates stiffness, pain, or functional limitations.
Baseline and post treatment after 6 weeks
Handheld Dynamometer
A handheld dynamometer (HHD) is a portable, objective tool used to measure isometric muscle strength at a fixed joint position. It records maximum muscle force in Newtons (N) or kilograms-force (kgf), with higher values indicating greater muscle strength.
Baseline and post treatment after 6 weeks
Secondary Outcomes (1)
SF-1 2 (Short form -1 2 Health Survey)
Baseline and post treatment after 6 weeks
Study Arms (2)
Low-Load Blood Flow Restriction Resistance Training
ACTIVE COMPARATORHip abductor strength training followed by low-load BFR resistance training
EXPERIMENTALInterventions
Participants will receive hip abductor strengthening for Weeks 2-4, followed by BFR resistance training during Weeks 5-6, under physiotherapist supervision. Exercises include side-lying hip abduction, clamshells, standing resisted hip abduction, and lateral band walks (3 sets of 10-15 repetitions or 10 lateral steps per direction), with 60-second rest intervals. Training will begin with bodyweight exercises, progressing to TheraBand resistance from Week 2, without BFR cuff application during hip exercises. Weeks 5-6: Participants will receive BFR training (knee extensions and leg presses) at 20-30% of 1RM, 70% arterial occlusion pressure (AOP), and 4 sets of 30-15-15-15 repetitions.
Participants will receive supervised low-load BFR training targeting quadriceps and hamstrings through seated knee extensions, leg presses (bilateral/unilateral), and progressive mini squats at 20-30% of 1RM.Each exercise includes 4 sets (30-15-15-15 repetitions), with 30-60 seconds of rest between sets while the cuff remains inflated, followed by immediate deflation after the final set.
Eligibility Criteria
You may qualify if:
- Both genders. Age 40-60 years. BMI (kg/m 2 ) \< 30 Have unilateral or bilateral knee OA. Have radiographic OA severity of Kellgren-Lawrence Grade I-II. Knee pain ≥3 months. Report pain intensity of ≥4-6/1 0 on Numeric Pain rating scale. Be able to walk independently without assistive devices
You may not qualify if:
- Total Knee replacement Deep venous thrombosis. Severe Cardiovascular disorders.(such as Acute myocardial infarction, peripheral arterial disease) Uncontrolled hypertension and diabetes. Acute knee injury within the last 6 months. Significant ligament tears (ACL, PCL, MCL, LCL). Knee surgery within the last 6-1 2 months. Lower limb Fractures
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Management & Technology
Lahore, Punjab Province, 54000, Pakistan
Related Links
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
October 17, 2026
First Posted
October 23, 2026
Study Start
October 20, 2026
Primary Completion (Estimated)
December 31, 2026
Study Completion (Estimated)
December 31, 2026
Last Updated
October 23, 2026
Record last verified: 2026-10
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, ICF
- Time Frame
- 6 months after the publication of the manuscript
- Access Criteria
- The data can be requested from the corresponding author.