- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04960865
Kinesio Taping and Calf Muscle Fatigue
August 25, 2022 updated by: Masood Khan, King Saud University
Effects of Kinesio Taping on Calf Muscle Fatigue in Collegiate Female Athletes
Muscle fatigue results in decreased ability in muscles to generate force.
Kinesio Tape may reverse the adverse effects of fatigue.
Thus this study will examine the acute effects of Kinesio tape on muscle fatigue.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The participants will be divided into three groups; 1. Experimental group: Kinesio tape with 50% tension will be applied; 2. Sham group: Kinesio tape without any tension will be applied; 3. Placebo group: Rigid tape without any tension will be applied.
Study Type
Interventional
Enrollment (Actual)
45
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Riyadh, Saudi Arabia, 11433
- King Saud University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
19 years to 25 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- Healthy cooperative individuals.
- Female athletes who were engaged in training at least 3 times a week.
- The subject should perform a minimum of 23 hell raises.
Exclusion Criteria:
- Musculoskeletal injuries, cardio-pulmonary vestibular and neurological complication and systemic disorder.
- Consumption of any pre-workout supplement in the last 6 months.
- Involvement in any other training program.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental Group
Participants will be applied Kinesio tape with 50% tension.
|
Kinesio tape will be applied to participants under tension.
|
|
Sham Comparator: Sham Group
Participants will be applied Kinesio tape without any tension.
|
Kinesio tape will be applied to participants without any tension.
|
|
Placebo Comparator: Placebo Group
Participants will be applied rigid tape without any tension
|
Rigid Taping will be applied.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of heel raises
Time Frame: 1 week.
|
Participants will have to perform heel raises in standing position untill thay are fatigued.
|
1 week.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Masood Khan, M.P.Th., King Saud University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 6, 2021
Primary Completion (Actual)
November 10, 2021
Study Completion (Actual)
December 22, 2021
Study Registration Dates
First Submitted
June 26, 2021
First Submitted That Met QC Criteria
July 13, 2021
First Posted (Actual)
July 14, 2021
Study Record Updates
Last Update Posted (Actual)
August 26, 2022
Last Update Submitted That Met QC Criteria
August 25, 2022
Last Verified
August 1, 2022
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- RRC-2021-05
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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