NCT06845657

Brief Summary

The aim of this randomized controlled trial is to find the effect of hip abductor strengthening exercises on pain, range of motion, functional disability and balance in patient with knee osteoarthritis.

Trial Health

57
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
40

participants targeted

Target at P25-P50 for not_applicable knee-osteoarthritis

Timeline
Completed

Started Mar 2025

Geographic Reach
1 country

1 active site

Status
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

First Submitted

Initial submission to the registry

February 20, 2025

Completed
5 days until next milestone

First Posted

Study publicly available on registry

February 25, 2025

Completed
6 days until next milestone

Study Start

First participant enrolled

March 3, 2025

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 16, 2026

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

March 26, 2026

Completed
Last Updated

March 11, 2025

Status Verified

March 1, 2025

Enrollment Period

12 months

First QC Date

February 20, 2025

Last Update Submit

March 9, 2025

Conditions

Keywords

Hip Abductor StrengtheningMuscle weaknessknee pain

Outcome Measures

Primary Outcomes (4)

  • Numeric Pain Rating Scale

    The Numeric Pain Rating Scale (NPRS) is a segmented numeric version of the visual analog scale which is used to assess pain. It scores ranges from 0-10, 0 means No pain and 10 means Severe pain. Patient will be asked to verbally report the pain score

    3 weeks

  • Western Ontario and McMaster Universities Osteoarthritis Index

    The Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) is a widely used, validated questionnaire assessing pain, stiffness, and physical function in patients with knee osteoarthritis. It consists of 24 items divided into three subscales: Pain (5 items), Stiffness (2 items), and Physical Function (17 items).

    3 weeks

  • Timed Up and Go test

    The Timed Up and Go (TUG) test measures the time taken by a participant to stand up from a standard chair, walk a distance of 3 meters, turn around, walk back to the chair, and sit down. It assesses dynamic balance and functional performance.

    3 weeks

  • Single leg stance

    The Single leg stance (SLS) Test is used to assess static postural and balance control. Participants are instructed to stand on one leg unassisted, with eyes open and hands on hips. The duration for which the position is maintained is recorded.

    3 weeks

Secondary Outcomes (1)

  • Range of Motion of Knee Joint

    3 weeks

Study Arms (2)

Hip Abductor Strengthening Exercises+ Conventional PT

ACTIVE COMPARATOR
Other: Hip Abductor Strengthening Exercises

Conventional PT

OTHER
Other: Conventional Treatment

Interventions

Hip Abductor Strengthening Exercises .1.side lying leg raise 2.clam shell(Frequency: 3 sets 10 reps in session 1-5) 3.standing hip abduction.4.pelvic lift training (Frequency: 3 sets 10 reps in session 6-9) .Conventional PT including 1-ROM 2- Stretching of hamstrings,calf,,rectus femoris (30 sec hold,15 sec relaxation period,3 rep) 3.knee isometrics (2 sets 10 rep in first 5 sessions and 3 sets 10 rep in next 4 sessions).total duration is 3 sessions per week for 3 consecutive weeks.

Hip Abductor Strengthening Exercises+ Conventional PT

Conventional PT including 1-ROM 2- Stretching of hamstrings,calf,rectus femoris (30 sec hold,15 sec relaxation period,3 rep) 3.knee isometrics (2 sets 10 rep in first 5 sessions and 3 sets 10 rep in next 4 sessions). Total duration is 3 sessions per week for 3 consecutive weeks

Conventional PT

Eligibility Criteria

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

You may qualify if:

  • Age group 40-60
  • Both genders male and female
  • Have had knee pain for 3 months or more
  • Report a minimum average overall pain severity of 4 on an 11-point numeric rating scale (NPRS) over the previous week
  • grade II and III on X-ray (Kellgren and Lawrence classification);
  • For participants with bilateral knee osteoarthritis, the more seriously affected side (as identified by the Kellgren-Lawrence grade of knee osteoarthritis and the pain intensity) was selected as the affected leg.
  • willing to participate in intervention program

You may not qualify if:

  • history of surgery of lower limb
  • Past knee fracture or malignancy
  • individuals with known hip OA and/or previous trauma affecting one or both hips
  • Intraarticular corticosteroid injection into the knee within previous 3 months.
  • Pregnancy

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

National Institute Of Rehabilitation Medicine G-8/2, Islamabad

Islamabad, Punjab Province, 46600, Pakistan

RECRUITING

MeSH Terms

Conditions

Osteoarthritis, KneeMuscle Weakness

Condition Hierarchy (Ancestors)

OsteoarthritisArthritisJoint DiseasesMusculoskeletal DiseasesRheumatic DiseasesMuscular DiseasesNeuromuscular ManifestationsNeurologic ManifestationsNervous System DiseasesPathologic ProcessesPathological Conditions, Signs and SymptomsSigns and Symptoms

Study Officials

  • KINZA ANWAR, MS-OMPT

    Riphah International University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

KINZA ANWAR, MS-OMPT

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 20, 2025

First Posted

February 25, 2025

Study Start

March 3, 2025

Primary Completion

February 16, 2026

Study Completion

March 26, 2026

Last Updated

March 11, 2025

Record last verified: 2025-03

Data Sharing

IPD Sharing
Will not share

Locations