- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06240013
Acute Effects of Foam Rolling and Proprioceptive Neuromuscular Facilitation Stretching
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
Status
Conditions
Intervention / Treatment
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
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Elif E Safran, asst. prof.
- Phone Number: 216 500 4047
- Email: elifesmabayraktar@hotmail.com
Study Locations
-
-
None Selected
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Istanbul, None Selected, Turkey, 34752
- Recruiting
- Acibadem University
-
Contact:
- Elif E Safran, asst. prof.
- Email: elifesmabayraktar@hotmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
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
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
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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.
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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
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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.
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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.
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Pre-intervention and immediately after the intervention
|
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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.
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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.
|
Pre-intervention and immediately after the intervention
|
Collaborators and Investigators
Sponsor
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
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2023-20-683
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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