Skip to content

Effects of Low Intensity Blood Flow Restriction on Clinical Outcomes in Women With Knee Osteoarthritis

Effects of Blood Flow Restriction on Clinical Outcomes in Women With Knee Osteoarthritis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04865692
Acronym
BFR
Enrollment
60
Registered
2021-04-29
Start date
2018-02-15
Completion date
2020-09-15
Last updated
2021-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteoarthritis, Knee

Brief summary

Objective is to compare the effects of routine physical therapy with and without low intensity blood flow restriction on pain and quadriceps muscle strength in women with knee osteoarthritis. A single blinded randomized controlled trial conducted at Department of Physiotherapy, University of Lahore Teaching Hospital, Defense Road, Lahore. Total 60 participants were randomly assigned in to two groups, with 30 in each group The intervention group received routine physiotherapy program combined with Low Intensity Blood Flow Restriction Technique (LI-BFR. While control group were treated with only routine physiotherapy. Dynamometer was used to assess the knee extensor strength while Knee injury and osteoarthritis outcome score was used to record any exacerbation in pain and effects of BFR on activities of daily living. Training load determined 20% of 1RM. Data analysis had done on SPSS version 23.

Detailed description

nonparametric test Friedman test was for comparison within the groups and Mann Whitney U test was used for comparison between groups. Randomization had done through the sealed envelope method. After allocation subjects had received their treatment protocals.

Interventions

OTHERBFRT

Patients of Interventional group were treated with routine physiotherapy program combined with LI-BFR consist of 10 minutes' session 3 per week for 12 weeks. In order to determine the training load 20% of 1RM, participants had performed knee extension in full range with a challenging weight. After each test, participants rated their perceived exertion level on (RPE) scale to determine the difficulty of the resistance. The derived 1RM was used to determine the 20% 1RM load used for low-load training. Blood flow restriction proximal to the working muscles achieved through using pressure cuffs. The cuff was applied to the proximal thigh. During week 1 the inflation pressure was 100mmHg. Final exercise pressure based the week of the training. Quadriceps size was measured by tape measures thigh

OTHERRoutine Physical Therapy

knee isometrics, resisted knee extension with chalanging weight 2 sets of 10 Reps with 5 sec hold

Sponsors

University of Lahore
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
45 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Diagnosed patients of grade II knee osteoarthritis * Patient's age 45-65

Exclusion criteria

* Bilateral knee replacement * Lower limb surgery in the last six months * Diagnosis of inflammatory joint or muscle disease * Chest pain during exercise or at rest; or need for supplemental oxygen * Pregnancy * Any systemic disease

Design outcomes

Primary

MeasureTime frameDescription
thigh muscle size12 weeksmeasuring tape was used to measure
Pain12 weekspain was measured through NPRS
Quadriceps muscle strength12 Weeksdynamometer was used to assess strength

Secondary

MeasureTime frame
Activities of daily living12 weeks

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026