NCT07593599

Brief Summary

The goal of this clinical trial is to learn if the macquire injury management group protocol and targeted knee exercise program works to treat knee osteoarthritis grade 2.This clinical trial compares the effects of macquire injury management group protocol and targeted knee exercise program on pain and range of motion and functional disability in patients with knee osteoarthritis grade 2.Adults with knee osteoarthritis grade 2 were included in this study. A total of 84 participants were divided into two groups with 42 patients in each group. One group received macquire injury management group protocol and the other group received targeted knee exercise program. Pain was assessed using the numeric pain rating scale and functional disability was measured using WOMAC index. Range of motion was also evaluated before and after treatment by universal goniometer.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
84

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Apr 2025

Geographic Reach
1 country

1 active site

Status
completed

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 Start

First participant enrolled

April 28, 2025

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 29, 2026

Completed
5 days until next milestone

Study Completion

Last participant's last visit for all outcomes

May 4, 2026

Completed
8 days until next milestone

First Submitted

Initial submission to the registry

May 12, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

May 18, 2026

Completed
Last Updated

May 18, 2026

Status Verified

May 1, 2026

Enrollment Period

1 year

First QC Date

May 12, 2026

Last Update Submit

May 12, 2026

Conditions

Keywords

OsteoarthritisKnee jointPain

Outcome Measures

Primary Outcomes (1)

  • Pain by numeric pain rating scale

    The level of pain was assessed using the Numeric Pain Rating Scale (NPRS), which is a simple and widely used tool for evaluating pain intensity. In this scale, individuals are asked to rate their pain on a scale from 0 to 10, where 0 indicates no pain and 10 represents the worst possible pain. Based on the categorization by Fiddiyanti et al. (2024), pain scores ranging from 1-3 are considered mild pain, 4-6 indicate moderate pain, and 7-10 represent severe pain. This scale provides a quick and reliable measure of a person's subjective pain experience.

    Baseline , 6th week and 12th week post intervention

Secondary Outcomes (2)

  • Range of motion by universal goniometer

    Baseline, 6th week and 12th week post intervention.

  • Functional disability by WOMAC index

    Baseline, 6th week and 12th week post intervention.

Study Arms (2)

macquire injury management group Protocol (MIMG )

EXPERIMENTAL

The macquire injury management group Protocol is known for its emphasis on soft tissue mobilization. The patients were made to lie down in a supine position and their knee joints were in an extended position during the treatment. In order to perform the soft tissue mobilization, the physiotherapist gently worked on the soft tissues of the knee joint for about two to three minutes using both his hands. In addition to the manual treatment method, the patients also underwent 45 minutes of physical therapy exercises

Procedure: Macquire injury management group protocol

Targeted knee exercise program

ACTIVE COMPARATOR

targeted knee exercise program , was aimed at improving the strength, proprioception, and stability of the knee joint. It comprised of progressively increasing knee exercises for the quadriceps (for example, straight leg raises and terminal knee extensions), hip abductors, and hamstrings. In addition to these exercises, there were also exercises to increase the stability of the joint by means of proprioceptive exercises involving single leg standing and dynamic stability exercises. Functional exercises including sit-to-stand and step up were also included. The intervention period lasted for 12 weeks with 3 sessions per week.

Procedure: Targeted knee exercise program

Interventions

The patients were made to lie down in a supine position and their knee joints were in an extended position during the treatment. In order to perform the soft tissue mobilization, the physiotherapist gently worked on the soft tissues of the knee joint for about two to three minutes using both his hands. In addition to the manual treatment method, the patients also underwent 45 minutes of physical therapy exercises

macquire injury management group Protocol (MIMG )

It comprised of progressively increasing knee exercises for the quadriceps (for example, straight leg raises and terminal knee extensions), hip abductors, and hamstrings. In addition to these exercises, there were also exercises to increase the stability of the joint by means of proprioceptive exercises involving single leg standing and dynamic stability exercises. Functional exercises including sit-to-stand and step up were also included. The intervention period lasted for 12 weeks with 3 sessions per week.

Targeted knee exercise program

Eligibility Criteria

Age40 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Both female and male subjects aged between 40 to 60 year
  • Diagnosed knee osteoarthritis, Grade II by Kellegren Lawrence.

You may not qualify if:

  • Any surgical procedure done for lower extremity
  • Any infection
  • Post traumatic knee stiffness
  • Secondary knee osteoarthritis
  • Peripheral vascular disease.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Johar pain relief center ,Lahore

Lahore, Punjab Province, 54000, Pakistan

Location

MeSH Terms

Conditions

Osteoarthritis, KneeOsteoarthritisPain

Condition Hierarchy (Ancestors)

ArthritisJoint DiseasesMusculoskeletal DiseasesRheumatic DiseasesNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: This is a randomized, parallel-group interventional study. Participants with Grade II Knee Osteoarthritis were randomly assigned in a 1:1 ratio to one of two treatment arms. Group A received macquire injury management group protocol and Group B received targeted knee exercise program. Both interventions were administered for the specifiec treatment period to compare their effectiveness on pain reduction and improvement in knee range of motion and functional disability.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Comparative Effects of Macquarie Injury Management Group Protocol and Targeted Knee Exercise Program on Pain, Range of Motion and Functional Disability in Patients with Grade II Knee Osteoarthritis

Study Record Dates

First Submitted

May 12, 2026

First Posted

May 18, 2026

Study Start

April 28, 2025

Primary Completion

April 29, 2026

Study Completion

May 4, 2026

Last Updated

May 18, 2026

Record last verified: 2026-05

Data Sharing

IPD Sharing
Will share

Only IPD used in the results publication will be shared.

Shared Documents
STUDY PROTOCOL, SAP, ICF, CSR
Time Frame
It will be available after completion of study.
Access Criteria
Data requests should be sent to the corresponding author. Access will be granted to qualified researchers for approved research proposals. Data will be de-identified before sharing.

Locations