- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06608836
Acute Effects of Cryotherapy on Muscle Properties
September 20, 2024 updated by: Gamze Aydin, Istanbul University - Cerrahpasa (IUC)
Acute Effects of Cryotherapy on Muscle Mechanical Properties and Muscle Activation Changes
The main aim of this study is to investigate the acute effects of cryotherapy on muscle mechanical properties, muscle strength, and activation changes in healthy subjects.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
What changes occur in muscle stiffness following cryotherapy application?
How does cryotherapy affect muscle strength?
How does cryotherapy impact muscle activation?
Are there differences in muscle mechanical properties, muscle strength, and muscle activation between different cryotherapy methods (ice massage and cold spray)?
How do the effects of cryotherapy on muscle mechanical properties, muscle strength, and muscle activation change over time?
Study Type
Interventional
Enrollment (Estimated)
52
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 Contact
- Name: Gamze Aydın, PhD
- Phone Number: +90 5377600256
- Email: gamze.tosun@okan.edu.tr
Study Contact Backup
- Name: Ozgur Surenkok, PhD
- Email: ozgur.surenkok@okan.edu.tr
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
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Being willing to participate in the study
- Being between the ages of 18 and 35
Exclusion Criteria:
- Having undergone orthopedic surgery involving the lower extremity
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: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Group 1
An ice massage will be applied to the quadrices muscle for a duration of 3 minutes.
|
an ice massage
|
|
Experimental: Group 2
A cold spray application will be performed to the quadrices muscle.
|
the cold spray
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
myoton pro device
Time Frame: 3 months
|
elasticity of muscle will assess by myoton pro device
|
3 months
|
|
muscle strength
Time Frame: 3 months
|
muscle strength will assess by dynanometer
|
3 months
|
|
electromyography device
Time Frame: 3 months
|
activation of quadriceps muscle will assess by electromyography device
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Gamze Aydın, PhD, Okan University
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 (Estimated)
December 15, 2024
Primary Completion (Estimated)
December 15, 2024
Study Completion (Estimated)
January 15, 2025
Study Registration Dates
First Submitted
September 12, 2024
First Submitted That Met QC Criteria
September 20, 2024
First Posted (Actual)
September 23, 2024
Study Record Updates
Last Update Posted (Actual)
September 23, 2024
Last Update Submitted That Met QC Criteria
September 20, 2024
Last Verified
September 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- IstanbulOkanUni
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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