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Developing a questionnaire which help Physiotherapist to treat individuals with Knee pain

Development, Validation, and Effectiveness of the SRIHER Knee Pain Screening Tool with Targeted Therapy in Physiotherapy Primary Care: A Randomized Controlled Clinical Trial - NIL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/12/077686
Enrollment
152
Registered
2024-12-05
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Health Condition 1: M239- Unspecified internal derangement of knee

Interventions

Intervention1: Experimental Group: The subjects in this group will receive exercise based on the Delphi study recommendation, SRIHER Targeted Therapy. SRIHER Targeted Therapy is a comprehensive assess

Sponsors

Sri Ramachandra Institute of Higher Education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: -Participants with Knee Pain aged above 18 to 55 years -Participants with sufficient English language comprehension -Participants who gave consent to participate in the study

Exclusion criteria

Exclusion criteria: -Participants with severe knee OA, in whom knee replacement is indicated. -Participants with a history of hip OA, lower limb joint replacement/ surgery, spine surgery -Participants with corticoid injection within the past one month. -Participants with any congenital or acquired deformity in the spine or lower limb -Participants Diagnosed with comorbidities - neurological conditions, psychiatric conditions, systemic diseases/cancer -Participants not able to come for follow ups / not willing to participate in the study -Participants with suspicion of chronic widespread pain

Design outcomes

Primary

MeasureTime frame
Knee Injury and Osteoarthritis Outcome Score (KOOS) questionnaire 30-Second Chair Stand Test Timepoint: at Baseline, at the end of the 1st week, 2nd week, 4th week, 6th week, 8th week, 10th week, 12th week

Secondary

MeasureTime frame
Global perceived effect Numerical rating scale Patient Reported Outcomes Measurement Information System (PROMIS) Knee muscle group strength using a hand-held dynamometer Timepoint: at Baseline, at the end of the 1st week, 2nd week, 4th week, 6th week, 8th week, 10th week, 12th week

Countries

India

Contacts

Public ContactProf Dr P Antony Leo Aseer

Sri Ramachandra Institute of Higher Education and Research

antonyleo@sriramachandra.edu.in09841544303

Outcome results

None listed

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