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Effectiveness Of MM & Kinesotaping In The Female Patients Of KO To Improve Pain & Functional Mobility RCT

Sponsor
Superior University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05868473
Collaborator
(none)
56
Enrollment
1
Location
2
Arms
5
Anticipated Duration (Months)
11.2
Patients Per Site Per Month

Study Details

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

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Mobilization With Movement
  • Diagnostic Test: Kinesotaping
 N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
56 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
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
Actual Study Start Date :
Apr 1, 2023
Anticipated Primary Completion Date :
Jun 1, 2023
Anticipated Study Completion Date :
Aug 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Other: Mobilization With Movement

Mobilization With Movement for Female Of Knee Osteoarthritis To Improve Pain And Functional Mobility

Diagnostic Test: Mobilization With Movement
Mobilization With Movement Female Of Knee Osteoarthritis To Improve Pain And Functional Mobility
Experimental: Kinesotaping

Kinesotaping for Female Of Knee Osteoarthritis To Improve Pain And Functional Mobility

Diagnostic Test: Kinesotaping
Kinesotaping Female Of Knee Osteoarthritis To Improve Pain And Functional Mobility

Outcome Measures

Primary Outcome Measures

  1. KOOS [6 Months]

    42 itens Questioner for Knee injury and Osteoarthritis Outcome Score

  2. Li Scale [6 Months]

    Lequesne Index is an11-item questionnaire designed to obtain information of a subjective nature,

Eligibility Criteria

Criteria

Ages Eligible for Study:
50 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Chaudary Muhammad Akram Teaching Hospital Lahore Punjab Pakistan

Sponsors and Collaborators

  • Superior University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Muhammad Naveed Babur, Principal Investigator, Superior University
ClinicalTrials.gov Identifier:
NCT05868473
Other Study ID Numbers:
  • DPT/Batch-Fall18/527
First Posted:
May 22, 2023
Last Update Posted:
May 22, 2023
Last Verified:
May 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:
Osteoarthritis
Osteoarthritis, Knee

Study Results

No Results Posted as of May 22, 2023