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Clinical Trials/CTRI/2022/11/046983
CTRI/2022/11/046983CompletedNot Applicable

Effects of kinesio taping over conventional physiotherapy exercise on pain,hamstring tightness and functional disability in knee osteoarthritis participants-a randomised controlled study

Not provided1 site in 1 country30 target enrollmentStarted: May 11, 2022Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
30
Locations
1
Primary Endpoint
Modified Western Ontario and McMaster Universities Index

Study Overview

Brief Summary

Osteoarthritis is a one of the major chronic joint disease worldwide. Cartilage is the central tissue affected by OA and causes subsequent symptoms, including joint pain, stiffness and joint swelling, which diminishes the range of motion. 30 Osteoarthritis participants will be randomly selected for the study from different physiotherapy OPDs of Rajkot. The participants will randomly divided into two groups: Experimental Group N= 15 and Conventional Group N=15. The Experimental group will receive Kinesiotaping and Conventional physiotherapy for 3 weeks and the Conventional group will receive the conventional physiotherapy protocol for 3 weeks. The Pre and Post treatment scores of NPRS, mWOMAC and Active knee extension test will be measured.The aim of this study to determine the effectiveness of additional Kinesio-taping (KT) with the conventional physiotherapy on pain, Hamstring tightness and functional disability in knee osteoarthritis participants The hypothesis of this study is there will be no difference in kinesio-taping over conventional physiotherapy exercises on pain, Hamstring tightness and knee functional disability in knee osteoarthritis participants. Experimental Hypothesis will be a significant difference in kinesio-taping over conventional physiotherapy exercises on pain, Hamstring tightness and knee functional disability in knee osteoarthritis participants

Study Design

Study Type
Interventional
Allocation
Random Number Table
Masking
Participant Blinded

Eligibility Criteria

Ages
45.00 Year(s) to 70.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • OA with pain at least in one knee for more than 2 months.
  • Pain intensity level between 4- 8 point of NPRS.
  • Participants that can walk independently.
  • Radiographic evidence or any prior medical diagnosis by a professional.

Exclusion Criteria

  • Any acute inflammation, contracture or surgery affecting the knee.
  • Pain during exercise or unstable medical conditions.
  • Patient that had NSAIDS injection few months back.
  • Any skin allergy, local skin lesion and infection.
  • Any allergic reaction after the treatment of Kinesiotherapy.

Outcomes

Primary Outcomes

Modified Western Ontario and McMaster Universities Index

Time Frame: Pre and post treatement(after 3 weeks)

Secondary Outcomes

  • NPRS(Pre and post treatment(after 3 weeks))
  • Active knee extension test(Pre and post treatment(after 3 weeks))

Investigators

Sponsor
Not provided

Study Sites (1)

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