NCT07298798

Brief Summary

Investigator study aims to compare the benefits of isometric exercise and closed kinetic chain exercises in strengthening programs to lessen pain along with enhance functionality in patients with PFP that are being associated with osteoarthritis and the assessment of PFP pertains to its recognition and the determination of significant therapeutic techniques. 70 Participants from the department of physiotherapy, Civil Hospital Karachi CHK and Dow University of Health Science (DIPMR) will be randomly assigned into two groups, an experimental group receiving closed kinetic chain exercise, and a control group receiving isometric exercises. The therapy will last four weeks, consisting of twelfth sessions. There will be 35 to 40 minutes in each session, Patients will be evaluated on primary outcome measure, pain intensity and functional limitation using various scales, including the numerical pain rating scale (NPRS) and Kujala/anterior knee pain scale (AKPS)

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
70

participants targeted

Target at P50-P75 for not_applicable knee-osteoarthritis

Timeline
19mo left

Started Nov 2023

Longer than P75 for not_applicable knee-osteoarthritis

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress62%
Nov 2023Nov 2027

Study Start

First participant enrolled

November 9, 2023

Completed
1.8 years until next milestone

First Submitted

Initial submission to the registry

August 26, 2025

Completed
4 months until next milestone

First Posted

Study publicly available on registry

December 23, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 28, 2026

Completed
1.7 years until next milestone

Study Completion

Last participant's last visit for all outcomes

November 8, 2027

Expected
Last Updated

January 6, 2026

Status Verified

December 1, 2025

Enrollment Period

2.3 years

First QC Date

August 26, 2025

Last Update Submit

December 31, 2025

Conditions

Outcome Measures

Primary Outcomes (2)

  • numerical pain rating scale (NPRS)

    1\. Numerical pain rating scale (NPRS) Pain intensity will measure using NPR scale (no need for permission), a reliable instrument retest reliability of 0.95 , 0 represents no pain and 10 represents severe suffering. 10= indicate worse pain 5= indicate moderate pain 0 = indicate no pain.

    12th sessions for four weeks ,outcome measures will take place both, at the baseline when intervention start and four weeks, following the intervention

  • . Kujala/ Anterior knee pain scale (AKPS)

    we will use the Kujala scale to measure functional limitations, a reliable instrument retest reliability of 0.9 in patient with PFPS, total 13 self-reported questionnaire. AKPS graded 0 to 100, 100 being the highest possible score with no pain and disability. Lower scores reflect greater pain and disability.

    12th sessions for four weeks, ,outcome measures will take place both, at the baseline when intervention start and four weeks, following the intervention

Study Arms (2)

GroupA . given treatment closed kinetic chain exercise

EXPERIMENTAL

Terminal knee extension, The patient stand facing the plinth with feet shoulder-width apart and a theraband looped around their knee and other plinth legs. patient bend their knees to a 30-degree angle, extend their leg against the band's resistance, and hold this position for six seconds. VMO squat, The position of patient, hip and knee will bend, weight of the body on feet and feet about shoulder width apart and turn the feet outward about 45 degrees and position hold for 30 second.

Behavioral: Terminal knee extension. .VMO squat. [TheraBand]

GroupB . given treatment isometric exercise SLR, Static quads.

EXPERIMENTAL

Static Quads The patient is long sitting or supine on their back, with a foam roll or towel behind their knee. Contract your quadriceps muscles while pressing down on the towel, maintaining this position for five seconds. Straight leg raising (SLR) The patient will be laying in supine, and before the exercise's lifting phase, a maximal isometric quadriceps contraction will be executed, followed by raising the leg to a height of 10cm above the plinth for 10 seconds.

Behavioral: Isometric exercises [knee roller]

Interventions

Terminal knee extension, The patient stand facing the plinth with feet shoulder-width apart and a theraband looped around their knee and other plinth legs. They bend their knees to a 30-degree angle, extend their leg against the band's resistance, and hold this position for six seconds. VMO squat, The position of patient, hip and knee will bend, weight of the body on feet and feet about shoulder width apart and turnthe feet outward about 45 degrees and position hold for 30 second.

GroupA . given treatment closed kinetic chain exercise

Static Quads The patient is long sitting or supine on their back, with a foam roll or towel behind their knee. Contract your quadriceps muscles while pressing down on the towel, maintaining this position for five seconds. Straight leg raising (SLR) The patient will be laying in supine, and before the exercise's lifting phase, a maximal isometric quadriceps contraction will be executed, followed by raising the leg to a height of 10 cm above the plinth for 10 seconds.

GroupB . given treatment isometric exercise SLR, Static quads.

Eligibility Criteria

Age35 Years - 60 Years
Sexfemale(Gender-based eligibility)
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Age between (35 to 60) years.
  • Gender: female.
  • The numerical pain rating scale (NPRS) is greater than three out often i.e. 3/10 score.
  • Patient experiences anterior knee pain due to such activities like squatting, prolonged sitting, running and stair climbing.
  • Patient with unilateral or bilateral knee pain with positive radiographic imaging.
  • Patients have grade 1 and 2 knee osteoarthritis (K\&L classification).

You may not qualify if:

  • Any past record of knee surgery.
  • Any past record of knee fracture.
  • Patients with any neurological disorder.
  • Cancer, malignancy or any bone tumor.
  • Comorbid like diabetes mellitus.
  • Any systemic inflammatory arthritis.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Saddar

Karachi, Pakistan

Location

Related Links

MeSH Terms

Conditions

Osteoarthritis, Knee

Interventions

Exercise

Condition Hierarchy (Ancestors)

OsteoarthritisArthritisJoint DiseasesMusculoskeletal DiseasesRheumatic Diseases

Intervention Hierarchy (Ancestors)

Motor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Experimental: GroupA .will be give treatment closed kinetic chain exercise i.e Terminal knee extension and VMO squat. GroupB .will be give treatment isometric exercise i.e SLR and Static quads.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

August 26, 2025

First Posted

December 23, 2025

Study Start

November 9, 2023

Primary Completion

February 28, 2026

Study Completion (Estimated)

November 8, 2027

Last Updated

January 6, 2026

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will not share

Locations