- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06351709
Acute Effects of Heat, Cold and Stretching on Knee Proprioception and Vertical Jump
February 5, 2025 updated by: Umut Paksoy, Istanbul Bilgi University
The aim of our study is to investigate the effects of heat, cold and stretching on knee proprioception and vertical jump.
60 healthy individuals were randomized into hot, cold, stretching and control groups of 15 each.
Pre-test and post-test measurements were made immediately after the application.
Knee proprioception was measured with a digital goniometer using the EPD (joint position sense) test.
Vertical jump heights were measured with contact mat by countermovement (CMJ) and squat splash (SQS) tests.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
60
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
-
-
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Istanbul, Turkey, 34218
- İstanbul Medipan Tıp Merkezi
-
-
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 between the ages of 18-30
- Agreeing to participate in the study and being informed Approving the Volunteer Consent Form
Exclusion Criteria:
- Having a history of surgery in the knee area
- Movement in lower extremity joints that may affect measurements have limitations.
- Having vision, hearing and balance impairment.
- May cause peripheral neuropathy and deep sensory loss, or loss of proprioception may be caused by other mechanisms having diseases.
- Have a neurological or systemic disease that affects balance and coordination have.
- Describing very severe pain in any part of the lower extremity.
- Being pregnant.
- Having cognitive dysfunction, lack of cooperation
- Having any disease that may cause inability to dry
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: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control Group
No intervention was applied to the control group.
|
|
|
Experimental: Hot Pack Group
Hot pack application was applied to the participants in the hot group to warm the extremities locally after the pre-tests were completed.
For the application of hotpack, which is a superficial and moist temperature agent, a Chattanooga ® brand hotpack pad (DJO Global, Chattanooga; CA, USA) with 10 slices and a size of 28 cm x 39 cm was used.
The hotpack pad was taken with the help of tongs from the Chattanooga ® brand hot pack boiler (DJO Global, Chattanooga; CA, USA) at 80° temperature and wrapped in a total of 5 layers with the help of 2 towels.
A hotpackpad was placed on each knee of the participant.
Hotpack pads were applied for 15 minutes in total.
|
Hot pack application was applied to the participants in the hot group to warm the extremities locally after the pre-tests were completed.
For the application of hotpack, which is a superficial and moist temperature agent, a Chattanooga ® brand hotpack pad (DJO Global, Chattanooga; CA, USA) with 10 slices and a size of 28 cm x 39 cm was used.
The hotpack pad was taken with the help of tongs from the Chattanooga ® brand hot pack boiler (DJO Global, Chattanooga; CA, USA) at 80° temperature and wrapped in a total of 5 layers with the help of 2 towels.
A hotpackpad was placed on each knee of the participant.
Hotpack pads were applied for 15 minutes in total.
|
|
Experimental: Cold Pack Group
For participants in the cold group, MSD ® brand cold pack gel (MVS Inmotion, MSD cold pack; Weftdijk 1502830, Belgium), 15 cm x 25 cm in size, was used to cool the extremities locally.
The cold pack gel, kept in the freezer, was wrapped in a paper towel and placed on the knee area.
Cold pack was applied to both knees for a total of 15 minutes.
|
For participants in the cold group, MSD ® brand cold pack gel (MVS Inmotion, MSD cold pack; Weftdijk 1502830, Belgium), 15 cm x 25 cm in size, was used to cool the extremities locally.
The cold pack gel, kept in the freezer, was wrapped in a paper towel and placed on the knee area.
Cold pack was applied to both knees for a total of 15 minutes.
|
|
Experimental: Stretching Group
Static stretching technique was applied to the quadriceps and hamstring muscle groups in both the dominant and non-dominant extremities of the participants in the stretching group.
All stretches were performed twice for 20 seconds with a 3-second rest.
|
Static stretching technique was applied to the quadriceps and hamstring muscle groups in both the dominant and non-dominant extremities of the participants in the stretching group.
All stretches were performed twice for 20 seconds with a 3-second rest.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Vertical Jump Distance Measurement
Time Frame: Before and immediately after application
|
Two types of vertical jump distances, squat jump and countermovement jump, were evaluated using a Fusion Sport ® brand jump meter (Fusion Sport, SmartJump; Colorado, USA) with a sensitivity of 1 nanometer, which is one thousandth of an antimeter.
Both tests were repeated a total of 3 times and the best results were recorded.
|
Before and immediately after application
|
|
Joint Position Sense Measurement
Time Frame: Before and immediately after application
|
For the active joint position sense test, which measures the individual's ability to find the taught target angle, a BASELINE ® brand digital goniometer (BASELINE ® Evaluation Instruments, Digital Absolute + Axis goniometer; NY, USA) with a sensitivity of 0.1° was used.
|
Before and immediately after application
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
November 2, 2020
Primary Completion (Actual)
February 20, 2021
Study Completion (Actual)
February 20, 2021
Study Registration Dates
First Submitted
April 2, 2024
First Submitted That Met QC Criteria
April 2, 2024
First Posted (Actual)
April 8, 2024
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
February 5, 2025
Last Verified
February 1, 2025
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- A47
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
product manufactured in and exported from the U.S.
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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