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Efficacy of knee, hip and foot strengthening exercises in knee pain

Efficacy of Physiotherapy intervention in management of Patellofemoral pain syndrome: A Randomized control trial - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/12/060674
Enrollment
100
Registered
2023-12-22
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

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

Conditions

Health Condition 1: M629- Disorder of muscle, unspecified

Interventions

Intervention1: Group B: Group B will receive knee and hip joint exercises for 3 weeks (4 times a week). Intervention2: Group C: Group C will receive knee joint exercise in combination of Diacutaneous

Sponsors

Guru Jambheshwar University of Science and Technology
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Subjects with anterior or retro patellar knee pain from at least 2 of the following activities regardless of the level of pain intensity: prolonged sitting, ascending and descending stairs, squatting, running, kneeling and hopping / jumping, Insidious onset of symptoms unrelated to a traumatic incident and persistent for at least 6 weeks, Both males and females, Age group between 18 to 40 years, Presence of pain on palpation of patellar facets, Positive results in the physical examination tests: patellofemoral grinding test and patellofemoral compression test.

Exclusion criteria

Exclusion criteria: Subjects with meniscal or other intra articular pathologic conditions, Subjects with cruciate or collateral ligament involvement, Subjects with patellar subluxation or dislocation, Subjects with previous surgery of the knee and hip joints, Subjects with knee and hip joints osteoarthritis, Pregnancy, Subjects with any conditions affecting the muscles strength like diabetes mellitus or rheumatoid arthritis, Non cooperative patients / participants not willing to participate in study

Design outcomes

Primary

MeasureTime frame
Pain, Patellofemoral joint pain and disability, Tenderness around patella, PCD (Patella Condyle Distance) Timepoint: The outcome measures will be evaluated at the baseline, at 3 weeks (end of treatment protocol) and followed up at 4 weeks

Secondary

MeasureTime frame
NILLTimepoint: NILL

Countries

India

Contacts

Public ContactDr Manoj Malik

Department of physiotherapy Guru Jambheshwar University of Science and Technology

manojmalikpt@gmail.com9896221262

Outcome results

None listed

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