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A study of the efficacy of continuous and intermittent blood flow restriction combined with exercise training in the intervention of patellofemoral pain syndrome

A study of the efficacy of continuous and intermittent blood flow restriction combined with exercise training in the intervention of patellofemoral pain syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091111
Enrollment
Unknown
Registered
2024-10-21
Start date
2024-10-26
Completion date
Unknown
Last updated
2024-10-28

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

Conditions

Patellofemoral Syndrome

Interventions

Continuous pressurization group (Group A):(1) Hip Joint Exercise: Resistance Exercise for Hip Adductors and External Rotators (2) Knee movement training: under continuous compression (2mins rest betwe
Intermittent Pressurization Group (Group B):(1) Hip Joint Exercise: Resistance Exercise for Hip Adductors and External Rotators (2) Knee joint exercise training: intermittent pressurization (2mins pre
Blank control group (Group C):Rehabilitation training services will be provided to subjects with rehabilitation needs at the end of this study intervention

Sponsors

Beijing Sport University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 26 Years

Inclusion criteria

Inclusion criteria: 1) Sex: male or female 2) Pain: peripatellar or retro-patellar (location); non-traumatic (nature); lasting 6 weeks and more (duration); Pain visual analog scale VAS = 30 mm (degree) 3) Meets the PFPS diagnostic criteria established by the 2016 International Patellofemoral Pain Symposium: peripatellar or retropatellar Pain in the peripatellar or retropatellar area that is exacerbated by at least 1 of the following functional activities: sitting, walking up and down stairs, squatting, running, kneeling, jumping, and walking. Sitting, walking up and down stairs, squatting, running, kneeling, jumping 4) Affected side: For subjects with bilateral symptoms, the limb with the more severe pain is selected.

Exclusion criteria

Exclusion criteria: 1) History of structural damage or lesions to the cartilage and ligaments of the knee joint. 2) Patellar dysplasia, patellar dislocation or subluxation, rheumatoid arthritis etc. 3) Participation in physical therapy or knee strengthening exercises within the last 6 months. 4) Invasive surgery (e.g. arthroscopy or intra-articular injection) on the affected knee within the last 12 months. 5) Involuntary pain or neurologic disease of the lumbar spine or other parts of the body 6) Unexplained chest pain, cardiovascular disease, renal disease, high risk of or history of deep vein thrombosis, abnormal blood pressure, headache, or other symptoms. cardiovascular disease, renal disease, high risk of deep vein thrombosis or history of deep vein thrombosis, abnormal blood pressure, dizziness attacks, syncope or lightheadedness during exercise. 7) Pregnancy and any contraindication to exercise

Design outcomes

Secondary

MeasureTime frame
Knee function;Muscle Thickness;Peak Torque/Body Weight (PT/BW);

Primary

MeasureTime frame
Pain;

Countries

China

Contacts

Public ContactXintong Li Gao qi

Beijing Sport University

ToooongLi@outlook.com+86 175 1571 5225

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026