- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04540341
Effectiveness of Mulligan Mobilization Technique and Core Stabilization Exercise With Knee Osteoarthritis
Investigation of the Effectiveness of Mulligan Mobilization Technique and Core Stabilization Exercises in Female Patients With Knee Osteoarthritis: A Randomized Controlled Single-Blind Study.
Osteoarthritis (OA) is a chronic disease process characterized by degeneration and inflammation in the joint cartilage and subchondral bone, synovial fluid and joint capsule. One of the most affected joints in OA is the knee joint, and the incidence of OA increases with age.
Different treatment approaches are used in the treatment of osteoarthritis. The aim of the study is to examine the effectiveness of Mulligan technique and core exercises applied to female patients with knee osteoarthritis. In addition, the investigators did not find any study examining the effect of Mulligan technique on static balance in the treatment of OA. This is the secondary aim of the study.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Denizli, Turkey, 20070
- Pamukkale University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Being diagnosed with knee osteoarthritis
- To be in the age range of 40-70
- No lower extremity surgery in the last 6 months.
- Agree to participate in the study
Exclusion Criteria:
- Having had hip-knee replacement surgery
- Surgery planned in the last 6 months
- Having received physical therapy in the last 6 months
- Having uncontrollable hypertension and cardiac problems
- Having been diagnosed with rheumatoid arthritis
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Mulligan mobilization group
Painless movement
|
Mulligan mobilization technique will be apply.
|
Experimental: Core stabilization group
Abdominal drawing-in maneuver
|
Core stabilization technique will be apply.
|
Active Comparator: conventional therapy group
Ultrasound TENS Hotpack
|
Conventional therapy exercise will be apply.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pain assessment
Time Frame: 10 minutes
|
Visual Analog Scale: This scale consists of a straight line with the end points defining extreme limits such as 'no pain at all', which is 0 cm, and 'pain as bad as it could be', which is 10cm.
|
10 minutes
|
Range of motion assessment
Time Frame: 10 minutes
|
Goniometric measurement
|
10 minutes
|
muscle strength assessment
Time Frame: 10 minutes
|
by handheld device (Commander Powertrack II brand)
|
10 minutes
|
functional level assessment
Time Frame: 5 minutes
|
Western Ontario and McMaster Universities Arthritis Index (WOMAC)
|
5 minutes
|
aerobic endurance assessment
Time Frame: 6 minutes
|
6 minute walk test
|
6 minutes
|
balance assessment
Time Frame: 5 minutes
|
Stand on one leg test
|
5 minutes
|
Timed Up& Go Test
Time Frame: 5 minutes
|
Timed Up& Go Test
|
5 minutes
|
assessment of quality of life survey
Time Frame: 5 minutes
|
Nottingham Health Profile
|
5 minutes
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 60116787-020/48052
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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