Myofacial PainNCT07174258
Myofascial Release Wıth Hamstring Shortness
A study testing Manual myofascial release group, Graston group and Home based exercise group in people with Myofacial Pain, run by Medipol University.
Trial summary
The aim of this study will be to investigate the effects of different myofascial release techniques on flexibility, balance, and performance in individuals with hamstring (HT) muscle shortness. Read more about this study
- Who is it for?
- Ages 18 to 60 years
- Conditions the study is for
- Myofacial Pain
- What is being tested?
- Manual myofascial release group, Graston group and Home based exercise group
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 45 participants
- Where
- No sites listed yet
- Study dates
- 15 Sep 2025to 30 Oct 2025
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 60 years
- All sexes
- No healthy volunteers
- Adult
Who may be able to join
- Being between 18 and 60 years of age,
- Visible shortening of the hamstring muscle,
- Passive straight leg raise (SLR) angle ≤ 70 degrees,
- No musculoskeletal problems in the lower extremity,
- First-time applicant for treatment of hamstring tightness, and
- Volunteering to participate in the study
Who cannot join
- Participating in intense physical activity within the last 24 hours
- Having had previous lower extremity trauma or surgery
- Having ankle instability
- Having neurological findings during the DBK test
- Having used analgesic, anti-inflammatory, or muscle relaxant medications within the last month
- Having obesity, diabetes, and/or metabolic syndrome
- Being pregnant
Trial locations and contacts
No sites are listed yet. Contact the study team or a site near you to ask about taking part.
About this study
Official title: The Effect of Different Myofascial Release Techniques on Flexibility, Balance, and Performance In Individuals With Hamstring Shortness
The aim of this study will be to investigate the effects of different myofascial release techniques on flexibility, balance, and performance in individuals with hamstring (HT) muscle shortness. A total of 48 participants with hamstring shortness will be randomly assigned into three groups: Group I (Manual Myofascial Release Group), Group II (Graston Group), and Group III (Home Exercise Group).
Read the detailed description
The aim of this study will be to investigate the effects of different myofascial release techniques on flexibility, balance, and performance in individuals with hamstring (HT) muscle shortness. A total of 48 participants with hamstring shortness will be randomly assigned into three groups: Group I (Manual Myofascial Release Group), Group II (Graston Group), and Group III (Home Exercise Group). The Graston and manual myofascial release groups will receive interventions twice a week for 4 weeks, totaling 8 sessions, in addition to being provided with a home exercise brochure. The home exercise group will receive only the brochure. All participants will be evaluated in terms of balance, flexibility, and performance both before and after the interventions. Balance will be assessed using the Single Leg Stance Test (SLST) and the Y Balance Test (YBT); flexibility will be assessed using the V Sit and Reach Test; agility and performance will be assessed using the Illinois Agility Test and the T-Drill Test.
- Conditions
- Myofacial Pain
- Being tested
- Manual myofascial release group, Graston group, Home based exercise group
- Keywords
- balance, manual myofascial relasing, performance
- Medical subject headings
- Facial Pain
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Manual myofascial release groupOther
Manual myofascial release techniques were applied to Group I on the feet, legs, and thighs, twice a week for 4 weeks.
Graston groupOther
Graston was applied to the gastrocnemius and hamstring muscles, and before the application, solid petroleum jelly was applied to the area to lubricate the surface. A stainless steel Graston instrument was used for the application, using a superficial sweep technique at a 30-degree angle for 2 minutes, followed by a deep sweep for 30 seconds.
Home based exercise groupOther
Group III received a home exercise program that included stretching exercises. They were asked to perform the exercises twice a week for four weeks, with 15-20 repetitions, without any intervention from a physiotherapist.
| Study group | Role | What they receive |
|---|---|---|
| Group I | Experimental | (Manual Myofascial Relasing group Receives: Other: Manual myofascial release group |
| Group II | Experimental | Graston Group Receives: Other: Graston group |
| Group III | Experimental | Home based exercise group Receives: Other: Home based exercise group |
What is being measured
The primary outcome is the main question the study is designed to answer.
V-Sit-Reach Test
This test can be easily performed without requiring a flexibility bench. The subject is asked to sit with their heels touching the floor and their toes pointing upward, with a distance of 30 cm between their feet. A straight line is drawn between their heels, which is considered the zero point. The subject reaches forward toward their heels without bending their knees. The best measurement is recorded as + or -.
Measured: at the beginning of the study and 4 weeks after the start
Single Leg Stance Test
It's one of the most frequently used tests by physiotherapists to assess postural stability. During the test, the patient is asked to keep their eyes open and their hands secured at the waist. They are asked to stand on one leg without any support, with the raised leg not touching the ground and avoiding any jumping, hopping, or other similar movements. This test is performed three times on each leg, and the average is calculated.
Measured: at the beginning of the study and 4 weeks after the start
Y Balance Test
The Y-shaped dynamic balance test is both economical and easy to perform compared to other balance tests and is an effective test for determining balance asymmetry. The Y-shaped balance test assesses individuals' dynamic balance in the anterior, posteromedial, and posterolateral directions. Before starting the test, the Y-shaped directions are determined. The average of the three distances is taken, and the ratio of the absolute distance to leg length is recorded.
Measured: at the beginning of the study and 4 weeks after the start
T Drill Test
Four cones are required for the course. Participants begin at cone "A" at the start command. They run straight to cone "B" and touch it with their right hand. They then sidestep to cone "C" and touch it with their left hand. They then sidestep to cone "D" and touch it with their right hand. Finally, they sidestep to cone "B" and touch it with their left hand. They then run back to cone "A" and stop the stopwatch as soon as they reach cone "A." The time is recorded in seconds. They run three times, resting between each repetition, and their best time is recorded.
Measured: at the beginning of the study and 4 weeks after the start
Illinois Agility Test
The Illinois test is administered to measure agility levels by considering individuals' ability to change direction. Before the test, participants are provided with the necessary information, and the course is explained in detail. Before starting the test, participants are given the opportunity to complete 3-4 trials at a slow pace. The test course is 5 meters wide and 10 meters long, with cones arranged 3.3 meters apart in the center.
This test consists of a 40-meter straight run and a 20-meter slalom run between cones, with 180-degree turns every 10 meters. After a full rest, the test is administered twice, and the best result is recorded in seconds.
Measured: at the beginning of the study and 4 weeks after the start
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted15 Sep 2025
- Study start15 Sep 2025 (estimated)
- Primary completion15 Oct 2025 (estimated)
- Study completion30 Oct 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Myofacial PainStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 45 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Medipol University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Ayca Nur Kilinc, Medipol University
- Investigators
- Merve Yılmaz Menek, PhD, Study director, Medipol University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07174258
- Sponsor's protocol ID
- E-10840098-202.3.02-3737
- Status last verified
- Sep 2025
- First submitted
- 8 Sep 2025
- Last updated
- 22 Sep 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 22 Sep 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effect of Different Myofascial Release Techniques on Flexibility, Balance, and Performance In Individuals With Hamstring Shortness
- ClinicalTrials.gov ID
- NCT07174258
- Acronym / sponsor ID
- E-10840098-202.3.02-3737
- Conditions
- Myofacial Pain
- Keywords
- balance, manual myofascial relasing, performance
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 45 participants (estimated)
- Lead sponsor
- Medipol UniversityUniversity, hospital or other
- Study start
- 15 Sep 2025 (estimated)
- Primary completion
- 15 Oct 2025 (estimated)
- Study completion
- 30 Oct 2025 (estimated)
- First posted
- 15 Sep 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The aim of this study will be to investigate the effects of different myofascial release techniques on flexibility, balance, and performance in individuals with hamstring (HT) muscle shortness. A total of 48 participants with hamstring shortness will be randomly assigned into three groups: Group I (Manual Myofascial Release Group), Group II (Graston Group), and Group III (Home Exercise Group).
Detailed description
The aim of this study will be to investigate the effects of different myofascial release techniques on flexibility, balance, and performance in individuals with hamstring (HT) muscle shortness. A total of 48 participants with hamstring shortness will be randomly assigned into three groups: Group I (Manual Myofascial Release Group), Group II (Graston Group), and Group III (Home Exercise Group). The Graston and manual myofascial release groups will receive interventions twice a week for 4 weeks, totaling 8 sessions, in addition to being provided with a home exercise brochure. The home exercise group will receive only the brochure. All participants will be evaluated in terms of balance, flexibility, and performance both before and after the interventions. Balance will be assessed using the Single Leg Stance Test (SLST) and the Y Balance Test (YBT); flexibility will be assessed using the V Sit and Reach Test; agility and performance will be assessed using the Illinois Agility Test and the T-Drill Test.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Group I | Experimental | Other: Manual myofascial release group(Manual Myofascial Relasing group |
| Group II | Experimental | Other: Graston groupGraston Group |
| Group III | Experimental | Other: Home based exercise groupHome based exercise group |
Who may qualify
- Ages
- 18 to 60 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult
Key inclusion criteria (6 listed)
- Being between 18 and 60 years of age,
- Visible shortening of the hamstring muscle,
- Passive straight leg raise (SLR) angle ≤ 70 degrees,
- No musculoskeletal problems in the lower extremity,
- First-time applicant for treatment of hamstring tightness, and
Key exclusion criteria (7 listed)
- Participating in intense physical activity within the last 24 hours
- Having had previous lower extremity trauma or surgery
- Having ankle instability
- Having neurological findings during the DBK test
- Having used analgesic, anti-inflammatory, or muscle relaxant medications within the last month
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Manual myofascial release groupManual myofascial release techniques were applied to Group I on the feet, legs, and thighs, twice a week for 4 weeks. | Other | Group I |
| Graston groupGraston was applied to the gastrocnemius and hamstring muscles, and before the application, solid petroleum jelly was applied to the area to lubricate the surface. A stainless steel Graston instrument was used for the application, using a superficial sweep technique at a 30-degree angle for 2 minutes, followed by a deep sweep for 30 seconds. | Other | Group II |
| Home based exercise groupGroup III received a home exercise program that included stretching exercises. They were asked to perform the exercises twice a week for four weeks, with 15-20 repetitions, without any intervention from a physiotherapist. | Other | Group III |
Primary outcome
V-Sit-Reach Test
Time frame: at the beginning of the study and 4 weeks after the start
This test can be easily performed without requiring a flexibility bench. The subject is asked to sit with their heels touching the floor and their toes pointing upward, with a distance of 30 cm between their feet. A straight line is drawn between their heels, which is considered the zero point. The subject reaches forward toward their heels without bending their knees. The best measurement is recorded as + or -.
Single Leg Stance Test
Time frame: at the beginning of the study and 4 weeks after the start
It's one of the most frequently used tests by physiotherapists to assess postural stability. During the test, the patient is asked to keep their eyes open and their hands secured at the waist. They are asked to stand on one leg without any support, with the raised leg not touching the ground and avoiding any jumping, hopping, or other similar movements. This test is performed three times on each leg, and the average is calculated.
Y Balance Test
Time frame: at the beginning of the study and 4 weeks after the start
The Y-shaped dynamic balance test is both economical and easy to perform compared to other balance tests and is an effective test for determining balance asymmetry. The Y-shaped balance test assesses individuals' dynamic balance in the anterior, posteromedial, and posterolateral directions. Before starting the test, the Y-shaped directions are determined. The average of the three distances is taken, and the ratio of the absolute distance to leg length is recorded.
T Drill Test
Time frame: at the beginning of the study and 4 weeks after the start
Four cones are required for the course. Participants begin at cone "A" at the start command. They run straight to cone "B" and touch it with their right hand. They then sidestep to cone "C" and touch it with their left hand. They then sidestep to cone "D" and touch it with their right hand. Finally, they sidestep to cone "B" and touch it with their left hand. They then run back to cone "A" and stop the stopwatch as soon as they reach cone "A." The time is recorded in seconds. They run three times, resting between each repetition, and their best time is recorded.
Illinois Agility Test
Time frame: at the beginning of the study and 4 weeks after the start
The Illinois test is administered to measure agility levels by considering individuals' ability to change direction. Before the test, participants are provided with the necessary information, and the course is explained in detail. Before starting the test, participants are given the opportunity to complete 3-4 trials at a slow pace. The test course is 5 meters wide and 10 meters long, with cones arranged 3.3 meters apart in the center. This test consists of a 40-meter straight run and a 20-meter slalom run between cones, with 180-degree turns every 10 meters. After a full rest, the test is administered twice, and the best result is recorded in seconds.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 22 Sep 2025.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Merve Yılmaz Menek, PhD study director
Medipol University
Questions about this trial
What is this clinical trial studying?
A study testing Manual myofascial release group, Graston group and Home based exercise group in people with Myofacial Pain, run by Medipol University.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 22 Sep 2025. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact AYÇA NUR KILINÇ, Msc (+905549904004, aycaa.kilinc@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
V-Sit-Reach Test (time frame: at the beginning of the study and 4 weeks after the start). The study lists 5 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Sep 2025.