- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04718363
Effects of Foam Rolling Prior to PNF Stretching on Hamstring Flexibility and Thigh Skin Temperature in Healthy Subjects (PNF)
January 28, 2021 updated by: Sinem Yenil, Dokuz Eylul University
Effects of Foam Roller Application Prior to Proprioceptive Neuromuscular Facilitation Stretching on Hamstring Flexibility and Thigh Skin Temperature in Healthy Subjects
There is no study investigating the hamstring flexibility and skin temperature after combined warm-up techniques especially PNF and foam rolling.
The main purpose of this study is to investigate the effects of foam roller application prior to proprioceptive neuromuscular facilitation stretching on hamstring flexibility and thigh skin temperature in healthy subjects.Secondly, it is aimed to compare the effects between non-vibration foam rolling and vibration foam rolling on measured parameters.
Study Overview
Status
Recruiting
Conditions
Detailed Description
In this study forty-eight subjects will be voluntarily recruited into the study according to inclusion criteria.
Participants will be randomly assigned to Vibration Foam Rolling + PNF stretching, Non-Vibration Foam Rolling + PNF stretching, only PNF stretching and control group.
Subjects will be evaluated before, immediately after and 30 minutes after intervention.
Hamstring flexibility will be evaluated with Active Knee Extension Angle (AKEA) Test and functionally Sit and Reach test.
Thigh skin temperature will be evaluated with thermographic imaging.
Study Type
Interventional
Enrollment (Anticipated)
48
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: Sinem Yenil
- Phone Number: 00904124924
- Email: sinemyenil_96@hotmail.com
Study Locations
-
-
-
İzmir, Turkey
- Recruiting
- Dokuz Eylül University
-
Contact:
- Sinem Yenil
- Email: sinemyenil_96@hotmail.com
-
Principal Investigator:
- Seher Ozyurek, PT, PhD
-
-
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- 18 years and older,
- Having limitation of 20 degrees or more in knee extension angle in AKEA test,
- Right side lower extremity dominance
Exclusion Criteria:
- History of lower extremity injury in the last 12 months
- Having neurological or psychological problem
- Doing a stretching based exercise recently
- History of pain in the lower body and extremity in the Nordic Musculoskeletal Questionnaire
- Having lower extremity deformity
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: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: Control Group
|
|
Experimental: PNF stretching group
|
A contract-relax PNF stretching technique will be applied to hamstring muscle.
|
Experimental: Non-vibration foam rolling prior to PNF stretching group
|
Prior to PNF stretching, participant will perform unilateral hamstring non-vibration foam rolling.
|
Experimental: Vibration foam rolling prior to PNF stretching group
|
Prior to PNF stretching, participant will perform unilateral hamstring vibration foam rolling (48 Hz).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in hamstring flexibility
Time Frame: Change from baseline hamstring flexibility at immediately after intervention and 30 minutes after intervention
|
Active Knee Extension test in supine position will be performed to measure hamstring flexibility.
|
Change from baseline hamstring flexibility at immediately after intervention and 30 minutes after intervention
|
Change in thigh skin temperature
Time Frame: Change from baseline skin temperature at immediately after intervention and 30 minutes after intervention
|
Posterior thigh skin temperature will be evaluated using thermographic imaging with infrared thermal camera.
|
Change from baseline skin temperature at immediately after intervention and 30 minutes after intervention
|
Change in functional hamstring flexibility
Time Frame: Change from baseline functional hamstring flexibility at immediately after intervention and 30 minutes after intervention
|
Sit-and-Reach test will be performed to measure functional hamstring flexibility.
|
Change from baseline functional hamstring flexibility at immediately after intervention and 30 minutes after intervention
|
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)
January 27, 2021
Primary Completion (Anticipated)
September 15, 2021
Study Completion (Anticipated)
September 15, 2021
Study Registration Dates
First Submitted
January 17, 2021
First Submitted That Met QC Criteria
January 20, 2021
First Posted (Actual)
January 22, 2021
Study Record Updates
Last Update Posted (Actual)
February 2, 2021
Last Update Submitted That Met QC Criteria
January 28, 2021
Last Verified
January 1, 2021
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 4742-GOA
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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