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To check the Effect of Manual therapy(Mulligan) in female patient with Knee Osteoarthritis

Effect of Mulligan Technique with Retro Walking on Functional Disability Quadriceps muscle strength and Quality of Life in Women with Knee Osteoarthritis A Randomized controlled trial - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/070138
Enrollment
34
Registered
2024-07-07
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Health Condition 1: M171- Unilateral primary osteoarthritisof knee

Interventions

Intervention1: mulligan mobilization with movement with retro walking: conventional treatment with mulligan mobilization with movement with retro walking. Treatment will be given 3 times/week for 6 we

Sponsors

none
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Subjects with unilateral knee osteoarthritis 2 Subjects have had knee osteoarthritis for more than 6 months. 3 Subjects aged between 40-60years 4 Only females will be included in this study. 5 Subjects having Grade 2 according to Kellgren-Lawrence Classification.

Exclusion criteria

Exclusion criteria: 1 Subjects have undergone lower limb surgery in the past 6 months. 2 Subjects taking medication (NSAIDS and steroids) 3 Subjects with traumatic injury at the knee joint, any neurologic condition affecting lower extremity function in the past 6 years 4 Knee deformities 5 Recent knee fracture in the past 6 months 6 Subject inability to understand Hindi or English

Design outcomes

Primary

MeasureTime frame
1.WOMAC Questionnaire (Western Ontario and McMaster Universities Osteoarthritis Index) 2.One repetition maximum 3.WHOQOL Questionnaire (Abbreviated WHO quality of life scale (WHOQOL-Brief) Timepoint: 1 Baseline 2 Post-intervention after 6 week

Secondary

MeasureTime frame
1.App-based goniometer (DrGoniometers, CDM S.r.L) 2.NPRS (Numerical Pain Rating Scale ) Timepoint: 1. baseline 2. Post-intervention (after 6 weeks)

Countries

India

Contacts

Public ContactDr Pooja Sharma

Manav Rachna International Institute of Research and Studies

pooja.fas@mriu.edu.in9999826604

Outcome results

None listed

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