The Sex-Specific Impact of a Single Foam Rolling Session on Peripheral Muscle Oxygenation

September 19, 2025 updated by: Pelin Pişirici

The Sex-Specific Impact of a Single Foam Rolling Session on Peripheral Muscle Oxygenation in Recreational Adults With Hamstring Tightness

The hamstring muscle, as a biarticular muscle, plays a crucial role in both hip extension and knee flexion and is part of the Superficial Back Line, which supports upright posture and prevents excessive flexion. Its continuous postural function requires endurance-oriented muscle fibers and sustained low-level muscle tone. Tightness in the hamstrings is commonly linked to postural imbalances and structural factors, contributing to gait alterations, low back pain, tendinopathy, and other musculoskeletal disorders. Improving hamstring flexibility is important for performance and injury prevention, with myofascial release-particularly self-myofascial release using foam rollers-being an effective method. Foam rolling reduces muscle tension, enhances tissue hydration, and may alleviate fascial adhesions. However, sex differences exist in connective tissue properties, potentially influencing outcomes. Limited research has explored foam rolling's impact on peripheral muscle oxygenation. This study aims to investigate the effect of foam rolling on hamstring muscle oxygen saturation in recreational individuals with tightness, with a hypothesis that females may show greater increases.

Study Overview

Status

Completed

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

Interventional

Enrollment (Actual)

36

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 Locations

    • Beşiktaş
      • Istanbul, Beşiktaş, Turkey (Türkiye), 34353
        • Bahçeşehir University

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:

  • 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

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: 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

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

Sponsor

Investigators

  • Principal Investigator: Gökhan Koçak, MD, Medipol University
  • Study Chair: Pelin Pisirici, PT, PhD, Bahçeşehir University, Faculty of Health Sciences

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)

June 1, 2025

Primary Completion (Actual)

August 1, 2025

Study Completion (Actual)

August 1, 2025

Study Registration Dates

First Submitted

July 14, 2025

First Submitted That Met QC Criteria

July 14, 2025

First Posted (Actual)

July 22, 2025

Study Record Updates

Last Update Posted (Estimated)

September 23, 2025

Last Update Submitted That Met QC Criteria

September 19, 2025

Last Verified

September 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

I need to talk with the coauthor.

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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