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Comparing the effect of whole-body neuromuscular training with exercises that focus only on hip strengthening to see which is better for improving knee function in patients with knee pain (patellofemoral pain syndrome).

Comparison of Core Neuromuscular Training versus Isolated Hip Strengthening Exercises on Reducing Pain and Improving Knee Functional Performance in Patients with Patellofemoral pain Syndrome - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/074518
Enrollment
66
Registered
2024-09-27
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Health Condition 1: M628- Other specified disorders of muscle

Interventions

Intervention1: Core neuromuscular training and isolated hip strengthening exrcises: This group will undergo core neuromuscular training in addition to routine physical therapy exercises for PFPS parti

Sponsors

Narayana hrudayalaya institute
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: years of age : 20-50 years History of at least 3 months of retro patellar pain during prolonged sitting, kneeling, climbing stairs, squatting, running, kneeling, hopping, jumping [ pain should be provoked during these activities] anterior knee pain with a minimum intensity of 3 or greater on the 10-cm visual analog scale (VAS) Subjects who are willing to participate in the study with symptoms of patellofemoral pain syndrome

Exclusion criteria

Exclusion criteria: x-ray & MRI indicative of meniscal injury or other intra-articular injury Increased laxity of cruciate or collateral or other pathologies including OA & knee joint effusion The subjects who fulfill the Inclusion & exclusion criteria and are willing to participate in the study will be assigned one of the groups after obtaining written informed consent

Design outcomes

Primary

MeasureTime frame
Visual Analog Scale (VAS) Pain levels will be measured by using the VAS scale on the day of assessment before intervention (pre-treatment) and after intervention (post-treatment). Timepoint: Visual Analog Scale (VAS) Pain levels will be measured by using the VAS scale on the day of assessment before intervention (pre-treatment) and after intervention (post-treatment). Using Kujala anterior knee pain scale This validated questionnaire assesses various aspects related to anterior knee pain and functional limitations, providing a comprehensive evaluation of PFPS symptoms and their impact on daily activities Both scales will be used after 4 weeks of intervention

Secondary

MeasureTime frame
Using Kujala anterior knee pain scale This validated questionnaire assesses various aspects related to anterior knee pain and functional limitations, providing a comprehensive evaluation of PFPS symptoms and their impact on daily activitiesTimepoint: After 4 weeks of intervention;kujala anterior knee pain scaleTimepoint: after 4 weeks of intervention;step down performance balance differences (anterior,posteromedial,posterolateral)Timepoint: after 4 weeks of treatment intervention;step down improvement balance differencesTimepoint: after 4 weeks of treatment intervention

Countries

India

Contacts

Public ContactAishwarya k

Narayana Hrudayalaya

nhaec@narayanahealth.org7829188432

Outcome results

None listed

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