- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07078448
- Original Trial
The Sex-Specific Impact of a Single Foam Rolling Session on Peripheral Muscle Oxygenation
The Sex-Specific Impact of a Single Foam Rolling Session on Peripheral Muscle Oxygenation in Recreational Adults With Hamstring Tightness
Study Overview
Status
Intervention / Treatment
Detailed Description
The hamstring muscle is a biarticular muscle that simultaneously contributes to both hip extension and knee flexion movements. From the perspective of myofascial continuity, the hamstring is part of the Superficial Back Line, whose general postural function is to support the body in a fully upright position and to prevent the tendency toward flexion. This continuous postural role throughout the day necessitates a higher proportion of slow-twitch, endurance-oriented muscle fibers within the muscular segments of this myofascial chain. The hamstrings, as components of this line, maintain a low-level but sustained tone during the day to support posture.
Tightness in the hamstring muscles frequently arises due to issues in structural connectivity such as segmental shortening or tension along the Superficial Back Line, prolonged postural loading, imbalances with the Superficial Front Line, or alterations in pelvic tilt. It has been demonstrated that hamstring tightness can lead to alterations in gait patterns, low back pain, patellar tendinopathy, plantar fasciitis, and hamstring injuries.
Hamstring flexibility is a fundamental factor for individuals to enhance their sports performance and maintain a healthy lifestyle. Achieving adequate range of motion or flexibility not only supports the optimal functioning of the musculoskeletal system but also contributes to the prevention of injuries and muscular imbalances. One of the methods employed to improve hamstring flexibility is myofascial release. According to a meta-analysis examining the immediate effects of myofascial release applied along the Superficial Back Line in adults, the majority of studies have reported improvements in joint range of motion (ROM) and muscle flexibility.
One technique known as self-myofascial release is the use of a foam roller. A foam roller is a rigid cylindrical tool made of foam, available in various densities and sizes. The pressure applied with a foam roller stimulates the Golgi tendon organ, thereby reducing muscle tension. Another possible effect is the enhancement of tissue hydration; during application, the soft tissues are compressed like a sponge, allowing fluids to permeate the tissues, facilitating movement between fascial layers, and increasing blood flow and tissue temperature. Additionally, it is hypothesized that foam rolling helps release fascial adhesions and reduces scar tissue formation.
The physiological properties of connective tissues differ between males and females. Women are generally considered to be more flexible compared to men and structurally demonstrate greater tissue compliance, exhibiting a higher capacity to stretch or adapt to deformation. Therefore, the effects observed following foam roller application may vary between sexes. One study sought to investigate the sex-specific effects of acute self-myofascial release on joint range of motion and muscle stiffness. Following a foam roller intervention consisting of two sets of 30 seconds, no significant difference was observed in soft tissue stiffness or joint range of motion among female participants; however, significant improvements were noted in the male group regarding plantar flexion, dorsiflexion, and plantar flexion range of motion. Analysis of covariance comparing sex differences revealed significant differences between groups in the medial region of the Achilles tendon and gastrocnemius muscle. These findings suggest that short-duration self-myofascial release sessions may be sufficiently effective in increasing ankle joint range of motion in males; however, further research is needed to generalize these results to females. Due to inconclusive findings regarding soft tissue stiffness across sexes, larger sample sizes are recommended to explore this topic further.
It is known that a single session of foam rolling can increase flexibility and joint range of motion; however, studies investigating the effect of foam rolling on peripheral muscle oxygenation remain limited. One study examined the effects of four different interventions-dynamic stretching combined with foam rolling, static stretching combined with foam rolling, static stretching alone, and eccentric exercise alone-on fascicle length, muscle-tendon unit stiffness, muscle oxygen saturation (SmO₂), and muscle performance. The results indicated a tendency for SmO₂ levels to decrease following eccentric exercise, while immediate increases were observed in the other three interventions. However, this research was not sex-specific and did not isolate the effect of foam rolling on the SmO₂ of the hamstring muscle.
The aim of the present study is to investigate the effect of foam rolling on muscle oxygen saturation of the hamstring muscle in recreational individuals with hamstring tightness. Our hypothesis is that muscle oxygenation will increase to a greater extent in females.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Beşiktaş
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Istanbul, Beşiktaş, Turkey (Türkiye), 34353
- Bahçeşehir University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Healthy individuals aged between 18 and 35 years
- Both male and female participants
- Absence of any known health conditions
- Hamstring tightness defined as ≥20° of knee flexion angle in Active Knee Extension test
Exclusion Criteria:
- Any neuromuscular or orthopedic disorders affecting the lower extremities
- Circulatory or vascular problems
- Respiratory or cardiovascular diseases
- Renal failure
- Presence of pain during measurements or exercise protocols
- Excessive skin sensitivity or active skin infection
- History of intense physical activity within the last 48 hours
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: female
foam roller intervention
|
FR will be applied to each hamstring muscle for 3 minutes per leg, totaling 6 minutes.
The pressure was self-regulated by participants, who are instructed to apply as much body weight as tolerable.
The rolling frequency is maintained at approximately 0.5 Hz, corresponding to one complete rolling cycle every 2 seconds.
Before the intervention, participants will receive verbal and visual instructions to ensure correct execution.
|
|
Experimental: male
foam roller intervention as the females received
|
FR will be applied to each hamstring muscle for 3 minutes per leg, totaling 6 minutes.
The pressure was self-regulated by participants, who are instructed to apply as much body weight as tolerable.
The rolling frequency is maintained at approximately 0.5 Hz, corresponding to one complete rolling cycle every 2 seconds.
Before the intervention, participants will receive verbal and visual instructions to ensure correct execution.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Muscle Oxygenation Assessment
Time Frame: baseline, immediately after the intervention, ten minutes after the baseline
|
Muscle oxygenation will be assessed using the MOXY Monitor, a portable, wireless, near-infrared spectroscopy (NIRS)-based device. The monitor will be placed on the belly of the right biceps femoris muscle and secured with an opaque elastic band to prevent ambient light interference. Measurements will be taken five minutes before and five minutes after the intervention session. During each measurement, the device will record data for 60 seconds, and the average SmO₂ (muscle oxygen saturation) value over this period will be used for analysis. |
baseline, immediately after the intervention, ten minutes after the baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Active Knee Extension (AKE) Test
Time Frame: baseline, immediately after the intervention, ten minutes after the baseline
|
The AKE test will be used as a secondary outcome measure to assess hamstring flexibility. Participants will lie supine with the non-tested leg extended. The tested leg will be positioned in 90° of hip flexion using a wooden box to stabilize the pelvis and thigh. Participants will actively extend the knee until a visible myoclonus occurs. They will then slowly lower the leg until the movement stops. At that point, the knee flexion angle will be measured using a goniometer. The average of three trials will be recorded for each leg. |
baseline, immediately after the intervention, ten minutes after the baseline
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Gökhan Koçak, MD, Medipol University
- Study Chair: Pelin Pisirici, PT, PhD, Bahçeşehir University, Faculty of Health Sciences
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- GP-FR-25G
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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