Close Chain and Open Chain Exercises With Blood Flow Restriction in Knee Osteoarthritis
Comparison of Close Chain and Open Chain Exercises With Blood Flow Restriction in Knee Osteoarthritis
1 other identifier
interventional
40
1 country
2
Brief Summary
The aim of this research is to find and compare the effect of close chain and open chain exercises with blood flow restriction in knee osteoarthritis on pain, range of motion, strength and functional performance in patients with knee osteoarthritis. Randomized controlled trials done at Railway General Hospital and Medistic Medical and Dental Center, Rawalpindi. The sample size was 40. The subjects were divided in two groups, 20 subjects in close chain exercises with blood flow restriction group and 20 in open chain exercises with blood flow restriction group. Study duration was of 4 weeks. Sampling technique applied was purposive non probability sampling technique. Only 45-75 years individual with grade 1 or 2 knee osteoarthritis were included. Tools used in the study are Numeric pain rating scale (NPRS), Western Ontario and McMaster Universities Arthritis Index (WOMAC), goniometer, crane scale (dynamometer), 30 s chair stand test. Data was analyzed through SPSS 21.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Feb 2026
Shorter than P25 for not_applicable
2 active sites
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
February 17, 2026
CompletedFirst Posted
Study publicly available on registry
February 23, 2026
CompletedStudy Start
First participant enrolled
February 28, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 20, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
June 30, 2026
ExpectedFebruary 23, 2026
February 1, 2026
3 months
February 17, 2026
February 17, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Numeric Pain Rating Scale (NPRS)
Changes from baseline pain intensity will be assessed using the Numeric Pain Rating Scale. The Numeric Pain Rating Scale is a subjective pain assessment tool ranging from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. Participants will be asked to rate their average knee pain intensity at rest and during activity. NPRS is widely used in clinical practice due to its simplicity, reliability, and responsiveness to change in musculoskeletal conditions.
[Time Frame: Pre intervention (Week 1) and Post intervention (Week 4)]
Secondary Outcomes (5)
Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)
[Time Frame: Pre intervention (Week 1) and Post intervention (Week 4)]
Knee Range of Motion (Flexion)
[Time Frame: Pre intervention (Week 1) and Post intervention (Week 4)]
Knee Range of Motion (Extension)
[Time Frame: Pre intervention (Week 1) and Post intervention (Week 4)]
Knee Muscle Strength
[Time Frame: Pre intervention (Week 1) and Post intervention (Week 4)]
30 Second Chair Stand Test
[Time Frame: Pre intervention (Week 1) and Post intervention (Week 4)]
Study Arms (2)
Closed kinetic chain exercises with blood flow restriction
ACTIVE COMPARATORClosed kinetic chain exercises with blood flow restriction and conservative therapy
Open kinetic chain exercises with blood flow restriction
ACTIVE COMPARATOROpen kinetic chain exercises with blood flow restriction and conservative therapy.
Interventions
Closed kinetic chain exercises with blood flow restriction and conservative therapy. Participants in this group will receive conventional physiotherapy including hot pack application over the knee for 10 minutes and TENS applied medial and lateral to the knee for 10 minutes prior to exercises. Mulligan mobilization with movement will be performed using pain free sustained tibial glides during active knee flexion and extension. Closed kinetic chain quadriceps strengthening exercises will include seated heel press, mini squats, wall slides, step ups, and step downs performed under blood flow restriction. Exercises will be performed using a standardized blood flow restriction protocol of 4 sets with repetitions of 30, 15, 15, and 15 at low load. Sessions will be conducted 3 days per week for 4 weeks, with a total of 12 sessions, each session lasting approximately 40 minutes.
Open kinetic chain exercises with blood flow restriction and conservative therapy. Participants in this group will receive conventional physiotherapy including hot pack application over the knee for 10 minutes and TENS applied medial and lateral to the knee for 10 minutes prior to exercises. Mulligan mobilization with movement will be performed using pain free sustained tibial glides during active knee flexion and extension. Open kinetic chain quadriceps strengthening exercises will include straight leg raises and knee extension exercises performed under blood flow restriction. Exercises will be performed using a standardized blood flow restriction protocol of 4 sets with repetitions of 30, 15, 15, and 15 at low load. Sessions will be conducted 3 days per week for 4 weeks, with a total of 12 sessions, each session lasting approximately 40 minutes
Eligibility Criteria
You may qualify if:
- Radiologic confirmation of KOA demonstrating Kellgren-Lawrence grade 1 or 2.
- Exhibited symptoms of unilateral KOA.
- Not taking any medications for KOA or receiving other treatments (including physiotherapy).
- Willing to participate without any neurological symptoms were the main objects of study.
You may not qualify if:
- A history of knee surgery or scheduled surgery.
- Kellgren-Lawrence grade 3 or 4.
- Systolic blood pressure over 160 mm Hg or under 100 mm Hg.
- Use of nonsteroidal anti-inflammatory drugs in the past 3 months.
- Any known vascular disease or any diagnosed blood pathology.
- Concomitant symptomatic hip or ankle pathology that could influence knee pain or function.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Medistic Medical and Dental Center
Rawalpindi, Pakistan
Pakistan Railway General Hospital
Rawalpindi, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Muhammad Affan Iqbal, PhD*
Riphah International University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 17, 2026
First Posted
February 23, 2026
Study Start
February 28, 2026
Primary Completion
May 20, 2026
Study Completion (Estimated)
June 30, 2026
Last Updated
February 23, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share