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

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

Study Locations

      • İzmir, Turkey
        • Recruiting
        • Dokuz Eylül University
        • Contact:
        • 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.

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

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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