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Effect of Patellofemoral Joint Mobilizations for knee pain

Comparative effect of Functional Patellofemoral Joint Mobilizations and Open-Pack Patellofemoral Joint Mobilization for Patellofemoral Pain Syndrome; A Randomized Clinical Trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220401054385N1
Enrollment
50
Registered
2022-06-05
Start date
2022-04-29
Completion date
Unknown
Last updated
2022-06-27

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

Conditions

Patellofemoral pain syndrome. Patellofemoral disorders

Interventions

Intervention 1: Intervention group (Group A)
1. Hot pack (10 min) 2.Grade 1-11 Functional patellofemoral joint mobilizations 3.Baseline Quadriceps strengthening exercise program. Intervention 2: Control group: Hot pack (10 min) 2.Grade 1-11open-

Sponsors

The University of Faisalabad
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Patients at the age of 18-35 years old Both gender Willingness to participate in the research Willingness for random allocation to either of the two groups Pain in the knee associated with, during or after the activity including stair ascending/descending, squatting, jumping, prolonged sitting etc Insidious onset of pain that is unrelated to trauma Patient having at least one positive test from these physical tests: 1)Patellofemoral grind test. 2) Patellar apprehension test.3) Step down test Visual analogue scale rating of anterior knee pain during daily activities at a minimum of 30 mm to 70 mm on 100 mm scale

Exclusion criteria

Exclusion criteria: Meniscal injury or any other articular injury. Knee ligament laxity. History of recent knee surgery History of recent patellar dislocation NSAID or corticosteriod drug use before testing within 24 hours

Design outcomes

Primary

MeasureTime frame
Pain in the anterior knee. Timepoint: Pain level will be measured before applying the intervention and then after 4 weeks after the completion of intervention. Method of measurement: Visual Analogue scale and anterior knee pain scale will be used to measure the pain.

Countries

Pakistan

Contacts

Public ContactDr. Sidra Majeed,PT

The University of Faisalabad

sidra.majeed@tuf.edu.pk+92 334 7731241

Outcome results

None listed

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