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Recruiting NCT07402408

Blood Flow Restriction Training in Knee Osteoarthritic Patients

No phase Interventional Knee Osteoarthristis

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Blood flow restriction training with Floss band, Blood flow restriction training with pneumatic cuff.
Who it may be relevant to
Registry conditions: Knee Osteoarthristis. Basic parameters: 40 years — 60 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Pakistan
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Comparison of Band Tissue Flossing Method and Traditional Cuff Method for Blood Flow Restriction Training in Patients With Knee Osteoarthritis

Overview

The aim of this study was to compare the effect of band tissue flossing method and traditional cuff method for blood flow restriction training on pain, range of motion, muscle strength and functional status in patients with knee osteoarthritis. Symptoms of this condition limit patient's ability to perform high load strengthening. Blood flow restraining training allows strengthening with lower loads. 46 subjects will be divided in two groups, 23 subjects in each group. knee extension and knee press exercises will be performed. In group A floss band was tied on thigh and in group B pneumatic cuff was applied on thigh. 40-60 years individual with knee osteoarthritis will be included. outcome measures will be assessed at baseline, after 1st session, after 2nd week and after 4th week.

Interventions

  • Other Blood flow restriction training with Floss band
    seated knee extension exercise and knee press exercises (4 sets; repetitions: 30,15,15,15) performed for four weeks with three sessions per week. Exercises performed with 20% of one repetition maximum. Floss band was tied at proximal thigh with 50% stretch in proximal to distal direction starting from above the patella and moving towards groin.
  • Other Blood flow restriction training with pneumatic cuff
    seated knee extension exercises and knee press exercises (4 sets; repetitions: 30,15,15,15) performed for four weeks with three sessions per week. Exercises performed with 20% of one repetition maximum. Clinical cuff was tied at proximal thigh with 40% of limb occlusion pressure.

Primary outcome measures

  • Numeric Pain Rating Scale (NPRS) [Time frame: 4th week]
Secondary outcome measures (6)
  • Knee Flexion Range of motion [Time frame: 4th week]
  • Knee Extension Range of Motion [Time frame: 4th week]
  • Quadriceps strength (dynamometer) [Time frame: 4th week]
  • Western Ontario and McMaster Universities (WOMAC) index [Time frame: 4th week]
  • 30 Second Sit to Stand Test (STS) [Time frame: 4th week]
  • Timed Up and Go Test (TUG) [Time frame: 4th week]

Eligibility criteria

Inclusion criteria

  • Age 40-60 years
  • Pain more than or equal to 3 on NPRS
  • Range of motion ≤ 100-degree flexion and ≤ 0-degree extension
  • Those who have knee osteoarthritis, according to KL (Grade 1 and 2)
  • Genders: Male and Female

Exclusion criteria

  • Cardiovascular condition e.g., hypertension, thromboembolism, lymphatic diseases etc.
  • Muscle/tendon/ ligament injuries
  • Any surgery, skin infection, trauma, pregnancy, fracture and fall
  • Patient with intra articular steroidal therapy with in last 6 months
  • Patient unwilling to participate and comply with the study session

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

Pakistan · 1 center
  • Pakistan Institute of Medical Sciences (P.I.M.S.) — Islamabad

Identifiers

NCT: NCT07402408 · Riphah/RCRAHS/REC/MS-PT/02171

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗