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Hamstring ContracturesNCT04193683

The Effect Of Myofascial Release Technique On Respiratory Parameters in Subjects With Short Hamstring Muscle

A study testing Myofascial Release Technique in people with Hamstring Contractures, run by Bezmialem Vakif University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The aim of this study was to investigate the effect of myofascial release technique on rib cage mobility, respiratory function, respiratory muscle strength and endurance in patients with hamstring muscle shortness. Read more about this study

Who is it for?
Ages 18 to 40 yearsHealthy volunteers can take part
Conditions the study is for
Hamstring Contractures
What is being tested?
Myofascial Release Technique
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
30 participants
Where
1 siteTurkey (Türkiye)
Study dates
15 Dec 2019to 28 Feb 2020
Phase
Interventional
Are there results?
None posted in the registry

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 40 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • more than 15 degrees knee flexion angle during popliteal angle test,
  • no generalized joint laxity according to Beighton Criteria, and
  • no musculoskeletal problems of lower extremities.

Who cannot join

  • history of lower extremity and/or axial skeletal fracture;
  • recent muscle, tendon injury in lower extremity;
  • history of lumbal disc herniation, arthritic and/or inflammatory disease;
  • obesity, diabetes and/or metabolic syndrome;
  • history of surgery in the last month,
  • using muscle relaxant medication in the last month;
  • received manual therapy in the last month

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Bezmialem Vakıf University

    Istanbul

Other trials in Turkey (Türkiye)

About this study

Official title: The Effect Of Myofascial Release Technique On Respiratory Functions, Respiratory Muscle Strength and Endurance in Subjects With Short Hamstring Muscle

The aim of this study was to investigate the effect of myofascial release technique on rib cage mobility, respiratory function, respiratory muscle strength and endurance in patients with hamstring muscle shortness.

Read the detailed description

Hamstring flexibility is important to maintain activities such as walking and running in daily life. Hamstring muscle shortness, commonly seen in the community, is a risk factor for many musculoskeletal pathologies. Clinical observations have shown that the shortness of the Hamstring muscle causes spinal malalignment. This deterioration of the spine alignment may adversely affect the rib cage expansion. Moreover, considering that the optimal length of the muscles provides optimal contraction, it was found that the spinal malalignment adversely affected the effective contraction of the diaphragm by changing the position of diaphragm. A different view is that, because the fascia functions as a single tissue surrounding the entire body, a restriction in the hamstring muscle can also cause a restriction in distal muscles such as diaphragm through the fascia.

There are many treatment methods used to increase the flexibility of the hamstring muscle. One of these methods is the myofascial release technique. In this technique, which targets both muscle and fascia, applying light and prolonged pressure provides the myo-fascial complex to reach its optimal length, resulting in the optimal function of the muscle. In our best knowledge, no study has evaluated the effect of myofascial release technique on respiratory parameters in patients with hamstring muscle shortness.

Being tested
Myofascial Release Technique, Sham-Ultrasound
Keywords
Hamstring Muscle, Hamstring Shortness, Hamstring Stiffness, Myofascial Release Technique, Respiratory Functions, Respiratory Muscle Strength, Respiratory Muscle Endurance

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Myofascial Release TechniqueOther

    Myofascial release technique will bi applied bottom of the feet, back of the legs and hamstrings in both extremities. The practitioner will decide how long she should stay in a region according to the feeling of releasing in the tissue. The technique will be applied to a region at least 3 times.

  • Sham-UltrasoundOther

    Sham-ultrasound will be applied to back of legs and thighs in both extremities without pressure and all parameters of the ultrasound device except the timer will be closed.

Study groups in NCT04193683
Study groupRoleWhat they receive
Sham-UltrasoundSham comparatorIntervention will include one session sham-ultrasound application to both lower extremities of participant. The total time will be 15 minutes.
Receives: Other: Sham-Ultrasound
Myofascial Release Technique+Sham-UltrasoundExperimentalIn addition to one session sham-ultrasound, the intervention will include one session myofascial release technique to both lower extremities of participant. The total time will be 30 minutes.
Receives: Other: Myofascial Release Technique; Other: Sham-Ultrasound

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change from baseline subcostal region chest expansion test at 60 minutes

    Chest Circumference Measurement

    Measured: 60 minutes

  2. Change from baseline xiphoid region chest expansion test at 60 minutes

    Chest Circumference Measurement

    Measured: 60 minutes

  3. Change from baseline axillary region chest expansion test at 60 minutes

    Chest Circumference Measurement

    Measured: 60 minutes

Secondary outcomes (7)
  1. Change from baseline maximum inspiratory pressure (MIP) at 60 minutes

    Respiratory Muscle Strength Test

    Measured: 60 minutes

  2. Change from baseline maximum expiratory pressure (MEP) at 60 minutes

    Respiratory Muscle Strength Test

    Measured: 60 minutes

  3. Change from baseline Forced Vital Capacity (FVC) at 60 minutes

    Respiratory Function Test

    Measured: 60 minutes

  4. Change from baseline Forced Expiratory Volume in 1 second (FEV1) at 60 minutes

    Respiratory Function Test

    Measured: 60 minutes

  5. Change from baseline FEV1/FVC at 60 minutes

    Respiratory Function Test

    Measured: 60 minutes

  6. Change from baseline Peak Expiratory Flow (PEF) at 60 minutes

    Respiratory Function Test

    Measured: 60 minutes

  7. Change from baseline Forced Expiratory Flow 25-75% at 60 minutes

    Respiratory Function Test

    Measured: 60 minutes

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted10 Dec 2019
  2. Study start15 Dec 2019
  3. Primary completion18 Feb 2020
  4. Study completion28 Feb 2020

Resources

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
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
30 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04193683
Sponsor's protocol ID
bvubcinar01
Status last verified
Sep 2026
First submitted
3 Dec 2019
Last updated
22 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Myofascial Release Technique in people with Hamstring Contractures, run by Bezmialem Vakif University at 1 site in Turkey (Türkiye).

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 3 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: finished, as of the sponsor's last update on 22 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change from baseline subcostal region chest expansion test at 60 minutes (time frame: 60 minutes). The study lists 3 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 2026.

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