Back to resultsEffectiveness Of MM & Kinesotaping In The Female Patients Of KO To Improve Pain & Functional Mobility RCT
Primary Purpose
Knee Osteoarthritis
Status
Recruiting
Phase
Not Applicable
Locations
Pakistan
Study Type
Interventional
Intervention
Mobilization With Movement
Kinesotaping
Sponsored by
About this trial
This is an interventional health services research trial for Knee Osteoarthritis
Eligibility Criteria
Inclusion Criteria: · Female patients of age ranging from age above 50 years suffering from knee Osteoarthritis will be included Exclusion Criteria: · Patients suffering from any type of Cancer effecting area at which treatment will be applied. Patients having joint replacement or knee disease effecting the performance. Having skin allergies to taping.
Sites / Locations
- Chaudary Muhammad Akram Teaching HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Experimental
Arm Label
Mobilization With Movement
Kinesotaping
Arm Description
Mobilization With Movement for Female Of Knee Osteoarthritis To Improve Pain And Functional Mobility
Kinesotaping for Female Of Knee Osteoarthritis To Improve Pain And Functional Mobility
Outcomes
Primary Outcome Measures
KOOS
42 itens Questioner for Knee injury and Osteoarthritis Outcome Score
Li Scale
Lequesne Index is an11-item questionnaire designed to obtain information of a subjective nature,
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT05868473
Brief Title
Effectiveness Of MM & Kinesotaping In The Female Patients Of KO To Improve Pain & Functional Mobility RCT
Official Title
Effectiveness Of Mobilization With Movement And Kinesotaping In The Female Patients Of Knee Osteoarthritis To Improve Pain And Functional Mobility: A Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 1, 2023 (Actual)
Primary Completion Date
June 1, 2023 (Anticipated)
Study Completion Date
August 31, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Superior University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
to find out the Effectiveness Of Mobilization With Movement And Kinesotaping In The Female Patients Of Knee Osteoarthritis To Improve Pain And Functional Mobility
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Knee Osteoarthritis
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
56 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Mobilization With Movement
Arm Type
Other
Arm Description
Mobilization With Movement for Female Of Knee Osteoarthritis To Improve Pain And Functional Mobility
Arm Title
Kinesotaping
Arm Type
Experimental
Arm Description
Kinesotaping for Female Of Knee Osteoarthritis To Improve Pain And Functional Mobility
Intervention Type
Diagnostic Test
Intervention Name(s)
Mobilization With Movement
Intervention Description
Mobilization With Movement Female Of Knee Osteoarthritis To Improve Pain And Functional Mobility
Intervention Type
Diagnostic Test
Intervention Name(s)
Kinesotaping
Intervention Description
Kinesotaping Female Of Knee Osteoarthritis To Improve Pain And Functional Mobility
Primary Outcome Measure Information:
Title
KOOS
Description
42 itens Questioner for Knee injury and Osteoarthritis Outcome Score
Time Frame
6 Months
Title
Li Scale
Description
Lequesne Index is an11-item questionnaire designed to obtain information of a subjective nature,
Time Frame
6 Months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
· Female patients of age ranging from age above 50 years suffering from knee Osteoarthritis will be included
Exclusion Criteria:
· Patients suffering from any type of Cancer effecting area at which treatment will be applied.
Patients having joint replacement or knee disease effecting the performance.
Having skin allergies to taping.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Roha Farooqi, DPT
Phone
+923453150991
Email
shuraimulhassan@gmail.com
Facility Information:
Facility Name
Chaudary Muhammad Akram Teaching Hospital
City
Lahore
State/Province
Punjab
Country
Pakistan
Individual Site Status
Recruiting
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Effectiveness Of MM & Kinesotaping In The Female Patients Of KO To Improve Pain & Functional Mobility RCT
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