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Comparative Effects of Kaltenborn Mobilization Versus Maitland Mobilization on Pain and Functional Status in Patients with Patellofemoral Pain Syndrome

Comparative Effects of Kaltenborn Mobilization Versus Maitland Mobilization on Pain and Functional Status in Patients with Patellofemoral Pain Syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250119064436N1
Enrollment
40
Registered
2025-04-17
Start date
2025-04-15
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Non specific knee pain. Disorders of muscles

Interventions

Intervention 1: Intervention group A will receive Kaltenborn Mobilization to improve the knee's range of motion, specifically focusing on enhancing flexion and extension. It will receive Moist heat,

Sponsors

The University of Faisalabad
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 55 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria for Patients: Age range between 25-55 years. Possible isolated pain to the anterior knee when the examiner applies pressure on the upper part of the patella while the patient engages in an isometric contraction of the quadriceps muscle. The test is also deemed positive if the patient is unable to maintain the contraction for more than two seconds. Have a history of patellofemoral pain syndrome, with symptoms persisting for at least the past 30 days. Participants must report pain during weight-bearing activities such as squatting, stair climbing, or prolonged sitting with bent knees. All participants must provide informed consent before enrollment in the study.

Exclusion criteria

Exclusion criteria: Deformities: Patients with structural abnormalities of the knee, such as valgus or varus deformities .Soft Tissue Injuries: Individuals with significant sprains, strains, or tears in the muscles, ligaments, or tendons around the knee .Fracture: Patients with any recent fractures of the femur, tibia, fibula, or patella.Dislocation of Patella: Individuals who have experienced a patellar dislocation.Patella Alta: Patients diagnosed with patella alta, where the patella is positioned higher than normal.

Design outcomes

Primary

MeasureTime frame
Patellofemoral pain. Timepoint: Patellofemoral pain will be measured three times. Before the start of 1st session, after 2 weeks and third time after 4 weeks. Method of measurement: Visual analogue scale.;Patellofemoral pain. Timepoint: Patellofemoral pain will be measured three times. Before the start of 1st session, after 2 weeks and third time after 4 weeks. Method of measurement: Visual analogue scale.

Secondary

MeasureTime frame
Range of Motion (ROM). Timepoint: Range of motion will be measured three times. Before the start of 1st session, after 2 weeks and third time after 4 weeks. Method of measurement: Goniometer.

Countries

Pakistan

Contacts

Public ContactDr. Amna Noor

The University of Faisalabad

amnanoor21028@gmail.com+92 309 8271779

Outcome results

None listed

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