Acute Effects of Foam Rolling and Proprioceptive Neuromuscular Facilitation Stretching

August 13, 2024 updated by: Acibadem University

Acute Effects of Foam Rolling and Proprioceptive Neuromuscular Facilitation Stretching During Warm-Up on Muscle Flexibility, Strength and Pain Threshold in Amateur Athletes

The hamstring muscle is one of the key elements in rehabilitation programs and sports activities that enable the restoration of optimal muscle length. Decreased flexibility in the hamstring muscle may disrupt the biomechanics of the waist and pelvis, leading to low back pain or musculoskeletal disorders.

This study aims to investigate the acute effects of foam rolling and proprioceptive neuromuscular facilitation stretching during warm-up on muscle flexibility, strength, and pain threshold in amateur athletes. According to our research, there is no study in this field in the literature.

H1: There is a difference between the acute effects of foam rolling exercise and PNF stretching exercise on muscle flexibility during warm-up in amateur athletes.

H2: There is a difference between the effects of foam rolling and PNF stretching exercises used as warm-up exercises on muscle strength.

H3: Foam rolling and PNF stretching exercises applied to the Hamstring muscle as a warm-up exercise make a difference in the pain threshold of the lumbar region and Hamstring muscle.

Study Overview

Detailed Description

Stretching techniques used in athletes are frequently and widely used due to many effects such as changing range of motion, comfortable movement maintenance, and removal. There is no consensus in the literature on which of the static, dynamic, and proprioceptive neuromuscular facilitation stretching techniques is most effective, as opposed to the types of stretching for flexibility. There is no clear benefit of different stretching techniques to muscle performance. Accordingly, in the literature, it is seen that proprioceptive neuromuscular facilitation stretching techniques show a greater increase in joint range of motion compared to other stretching techniques.

Recently, the use of foam rolling has become widely used in sports applications due to similar effects seen in stretching and the hypothesized presence of a curative effect on muscle performance. There is not enough research on the extent of foam rolling during warm-up exercises to increase flexibility and muscle strength.

The hamstring muscle is one of the key elements in harmonious programs and sports activities that ensure the restoration of optimal muscle length. The emergence of the output in the hamstring muscle may disrupt the biomechanics of the waist and pelvis, causing low back pain or musculoskeletal disorders.

This study aims to investigate the acute effects of foam rolling and proprioceptive neuromuscular facilitation stretching on muscle input, strength, and pain intensity during nutrition in amateur athletes.

Study Type

Interventional

Enrollment (Estimated)

80

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

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
  • Being an amateur athlete

Exclusion Criteria:

  • Hypermobility
  • History of hamstring injury in the last 6 months
  • Diagnosed orthopedic problems
  • Surgery in the lower extremity or spine
  • Back pain
  • Presence of systemic or neurological disorders

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: Crossover Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Group 2 Training Program
5 minutes of light aerobic cycling, unilateral 4*30 seconds on the dominant leg - 2 minutes in total proprioceptive neuromuscular facilitation stretching training
A PNF stretching protocol will be implemented with each participant assuming a tall sitting position on a solid, flat surface with their knees extended as much as possible. At this moment, the participant will be asked to perform maximum isometric hamstring muscle contraction for 5 seconds, followed by 5 seconds of relaxation and 20 seconds of stretching.
Experimental: Group 1 Training Program
5 minutes of light aerobic cycling, unilateral 2*60 sec on dominant leg - 2 min foam rolling training in total
Participants will take a long sitting position on a solid and flat surface, positioning their arms back and transferring their body weight to their palms. The foam roller to be applied to the dominant side will be placed under the hamstrings and slowly moved back and forth from the ischial tuberosity to the popliteal fossa, applying pressure for 2 minutes.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Hamstring Flexibility
Time Frame: Pre-intervention and immediately after the intervention
Hamstring flexibility (mm) will be evaluated with the sit-reach test. Baseline® Sit and Reach Flexibility Measurement device will be used for testing. Participants will sit on the floor with their lower extremities extended and together; Their backs and hips will be supported against the wall, and the soles of their feet will be placed on the edge of the device. Participants will then extend their arms forward, with both hands facing down and one hand on top of the other (always the same hand on top). Participants will then be asked to lie forward and slide their hands as far as possible on the measurement scale without bending their knees. Measurements will be repeated three times and the average value will be recorded.
Pre-intervention and immediately after the intervention
Hamstring Muscle Strength
Time Frame: Pre-intervention and immediately after the intervention
Strength measurement of the participants' Hamstring muscles will be made using a digital hand dynamometer (J Tech Commender Muscle Tester). Participants will be instructed to sit in a fairly upright position in a chair, with their arms crossed in front of their chest and their legs hanging over the edge, with their knees and hips flexed at 90°. For isometric knee flexion muscle measurement evaluation, the dynamometer will be placed in the sural triceps region (5 cm proximal to the lateral malleolus). Participants press the dynamometer as hard as possible for three seconds, while the assessor will provide resistance, preventing any movement to achieve an isometric contraction.
Pre-intervention and immediately after the intervention
Pain Threshold
Time Frame: Pre-intervention and immediately after the intervention
An algometer (Dolorimeter) will be used to objectively measure pain threshold and pain tolerance. The pain threshold value due to the pressure to be applied to the hamstring muscle and waist area will be measured using an electronic algometer (Algometer, Baseline FDK 10) while the athlete is in a prone position on the bed. The algometer will be applied vertically to the most painful point, increasing the pressure by 1kg/cm2 every three seconds until the patient feels pain. The pressure value that causes the feeling of pain will be determined as the pain threshold.
Pre-intervention and immediately after the intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Lower Extremity Muscle Strength
Time Frame: Pre-intervention and immediately after the intervention

A vertical jump test will be performed to evaluate the participants' lower extremity muscle strength. The measurement has two stages; measuring reach height, measuring jump height.

  1. Measuring reach height: The athlete stands with his feet flat on the ground. He/she is asked to raise his/her arms up from the side of the body. The point his fingers reach is recorded.
  2. Measuring the jump height: The athlete is asked to move away from the wall. The starting position is with feet shoulder-width apart and knees extended. After the hips and knees are bent, the athlete is asked to jump. The athlete reaches the highest point he can reach with his hands. The length of this point is recorded.
Pre-intervention and immediately after the intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Elif E Safran, asst. prof., Acibadem University
  • Principal Investigator: Hayri E Yılmaz, Acibadem University
  • Study Chair: Birce B Çelik, Acibadem University
  • Study Chair: Mahmut E Bükülmez, Acibadem University
  • Study Chair: Eren Çekiç, Acibadem 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 (Actual)

April 16, 2024

Primary Completion (Estimated)

December 1, 2024

Study Completion (Estimated)

February 1, 2025

Study Registration Dates

First Submitted

January 12, 2024

First Submitted That Met QC Criteria

January 24, 2024

First Posted (Actual)

February 2, 2024

Study Record Updates

Last Update Posted (Actual)

August 14, 2024

Last Update Submitted That Met QC Criteria

August 13, 2024

Last Verified

August 1, 2024

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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