Comparison of Aquatic and Land-Based Mulligan Mobilization With Movement in Knee Osteoarthritis
1 other identifier
interventional
66
1 country
1
Brief Summary
This study aims to compare the effects of aquatic and land-based Mulligan mobilization with movement in individuals with knee osteoarthritis, with particular focus on their impact on pain and functional outcomes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable knee-osteoarthritis
Started May 2026
Shorter than P25 for not_applicable knee-osteoarthritis
1 active site
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
March 16, 2026
CompletedFirst Posted
Study publicly available on registry
March 20, 2026
CompletedStudy Start
First participant enrolled
May 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 15, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
August 15, 2026
May 6, 2026
April 1, 2026
4 months
March 16, 2026
April 30, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Visual Analog Scale (VAS)
The Visual Analog Scale (VAS) is a straightforward and reliable method for evaluating pain on a continuous visual range.The extreme limits of pain are represented by the straight line's ends, where 0 indicates no pain, and 10 indicates the worst pain a person has ever felt.
4 weeks
Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)
It is used to assess activities of daily living, functional mobility, gait, general health, and quality of life. It has 24 items divided into 3 subscales: pain (5 items), stiffness (2 items), and physical function (17 items). The scores range from 0 to 4 for each subscale. The score ranges from 0 to 96, where zero indicates no pain, stiffness, and functional limitation. Higher scores indicate worse pain, stiffness, and functional limitation.
4 weeks
Secondary Outcomes (3)
Range of Motion of Knee
4 weeks
Time Up and Go (TUG)
4 weeks
Intrinsic Motivational Inventory (IMI)
4 weeks
Study Arms (2)
Aquatic Mobilization with Movement
EXPERIMENTALMulligan Mobilization with Movement will be administered in the aquatic environment using a belt, following identification of the most pain-free glide in addition to stretches and strengthening of lower limb. The technique will be performed for 10 repetitions over 3 sets and will be progressively advanced from non-weight-bearing mobilization to mobilization with overpressure, and subsequently to weight-bearing mobilization as tolerated by the patient.
Land Mobilization with Movement
OTHERMulligan Mobilization with Movement will be administered on land using a belt, following identification of the most pain-free glide, in addition to stretches and strengthening of the lower limb. The technique will be performed for 10 repetitions over 3 sets and will be progressively advanced from non-weight-bearing mobilization to mobilization with overpressure, and subsequently to weight-bearing mobilization as tolerated by the patient.
Interventions
This intervention group will receive treatment for four weeks inside the pool, in addition to the conventional knee osteoarthritis rehabilitation protocol.
This intervention group will receive treatment for four weeks on land, in addition to the conventional knee osteoarthritis rehabilitation protocol.
Eligibility Criteria
You may qualify if:
- Age 40-65 years
- Bilateral knee osteoarthritis diagnosed according to the American College of Rheumatology Clinical Classification system for at least 1 year
- Kellgren \& Lawrence grade 2 and 3
- Able to walk independently/unaided
You may not qualify if:
- Active participation in gyms, pool(swimming), or any other physical activity
- Intra-articular corticosteroid injections in the last 3 months or hyaluronic knee injection in the last 6 months.
- History of lower limb trauma/surgery, presence of fracture or lower limb deformity, or planned surgery within the study period
- Any diagnosed severe cardiovascular, pulmonary, neurological, or psychological disease/impairment.
- Individuals with aquaphobia (fear of water), discomfort performing aquatic exercises, or allergy/sensitivity to chlorine or other pool treatment chemicals.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Bahria Active
Rawalpindi, Pakistan
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Suman Sheraz, PhD
Riphah International University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 16, 2026
First Posted
March 20, 2026
Study Start
May 1, 2026
Primary Completion (Estimated)
August 15, 2026
Study Completion (Estimated)
August 15, 2026
Last Updated
May 6, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share