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Hamstring Muscle Shortness and Elastographic ExaminationNCT04118231

Effects of Dry Needling, Static Stretching and IASTM in People With Hamstring Muscle Shortness

A study testing Dry needling, IASTM and Static stretching in people with Hamstring Muscle Shortness and Elastographic Examination, run by Gazi University at 2 sites 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

This randomized controlled trial compared the effects of dry needling, static stretching and instrument-assisted soft tissue mobilization (IASTM), each applied three times per week for four weeks, with a no-intervention control group in adults with hamstring muscle shortness. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
What is being tested?
Dry needling, IASTM and Static stretching
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
2 sitesTurkey (Türkiye)
Study dates
1 Dec 2022to 2 May 2023
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 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Age 18 years or older
  • Hamstring tightness, defined as passive hip flexion range of motion < 65° on the straight leg raise test without neurological signs
  • No diagnosed chronic condition
  • Voluntary participation and signed informed consent

Who cannot join

  • Intense exercise within the previous 24 hours
  • History of lower-extremity trauma or surgery
  • History of hamstring injury
  • Low back or sciatic pain or numbness
  • Ankle instability
  • Neurological signs during the straight leg raise test
  • Lower-extremity hyperalgesia
  • Pregnancy

Trial locations and contacts

2 sites in 1 country.

Turkey (Türkiye)2 sites
  • Gazi University

    Ankara, 06500

  • Gökhan maraş

    Ankara, 06500

Other trials in Turkey (Türkiye)

About this study

Official title: Comparison of the Effects of Dry Needling, Static Stretching and Instrument Assisted Soft Tissue Mobilization Techniques on Function, Performance and Muscle Structure in People With Hamstring Muscle Shortness

This randomized controlled trial compared the effects of dry needling, static stretching and instrument-assisted soft tissue mobilization (IASTM), each applied three times per week for four weeks, with a no-intervention control group in adults with hamstring muscle shortness. Outcomes included joint range of motion, muscle strength, performance and muscle structure, and hamstring stiffness assessed with ultrasound shear-wave elastography.

Read the detailed description

Randomized, parallel-group, four-arm trial in adults with hamstring tightness (passive hip flexion < 65° on the straight leg raise test). Sixty participants were randomized using block randomization to IASTM, dry needling, static stretching or a no-intervention control group (15 per group). Interventions were applied to the dominant-limb hamstrings three times per week for four weeks (12 sessions); dry needling was performed by a physiotherapist under the supervision of a physical medicine and rehabilitation specialist. Outcomes were assessed at baseline and three days after the 12th session. Data collection was postponed because of the COVID-19 pandemic and took place after approval by the Gazi University Faculty of Medicine Clinical Research Ethics Committee (07.11.2022, No. 812).

Being tested
Dry needling, IASTM, Static stretching
Keywords
Hamstring Shortness, Dry Needling, Elastography

What participants receive

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

  • Dry needlingOther

    Dry needling of the hamstring muscles at three standardized sites near the motor points (two over the biceps femoris, one over the semitendinosus/semimembranosus) using sterile, single-use stainless-steel needles and a fast in-and-out technique, approximately one minute per site.

  • IASTMOther

    Instrument-assisted soft tissue mobilization of the hamstring muscle group with a stainless-steel instrument, applied with distal-to-proximal sweeping strokes for 5 minutes per session.

  • Static stretchingOther

    Manual passive static stretching of the hamstrings in supine with the knee extended: five 30-second stretches separated by 30-second rest periods (5 minutes per session).

Study groups in NCT04118231
Study groupRoleWhat they receive
Dry needlingExperimentalDry needling of the hamstring muscles at three standardized sites near the motor points (two over the biceps femoris, one over the semitendinosus/semimembranosus) using sterile, single-use stainless-steel needles and a fast in-and-out technique, approximately one minute per site. Performed by a physiotherapist under the supervision of a physical medicine and rehabilitation specialist.
Receives: Other: Dry needling
Control groupNo interventionNo intervention; outcomes assessed at the same time points as the intervention groups.
IASTMExperimentalIASTM applied to the dominant-limb hamstrings, 3 sessions per week for 4 weeks (12 sessions).
Receives: Other: IASTM
Static stretchingExperimentalStatic stretching applied to the dominant-limb hamstrings, 3 sessions per week for 4 weeks (12 sessions).
Receives: Other: Static stretching

What is being measured

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

  1. Range of motion

    The amount of hip flexion will be measured using a digital inclinometer.

    Measured: Baseline and 3 days after the 12th session (week 4)

  2. Muscle Strength

    Muscle strength will be assessed in newton using a digital hand dinanometer.

    Measured: Baseline and 3 days after the 12th session (week 4)

  3. Vertical jump

    The amount of vertical jump will be calculated from the value of cm by the tape measure fixed to the wall.

    Measured: Baseline and 3 days after the 12th session (week 4)

  4. Muscle stiffness

    Muscle stiffness will be evaluated by an expert radiologist using ultrasound elastography.

    Measured: Baseline and 3 days after the 12th session (week 4)

Timeline

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

  1. First posted8 Oct 2019
  2. Study start1 Dec 2022
  3. Primary completion1 May 2023
  4. Study completion2 May 2023

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
Model description
Four-arm parallel-group randomized trial with 1:1:1:1 allocation (block randomization).
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
60 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04118231
Sponsor's protocol ID
2019-114
Status last verified
Oct 2026
First submitted
3 Oct 2019
Last updated
16 Oct 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 Dry needling, IASTM and Static stretching in people with Hamstring Muscle Shortness and Elastographic Examination, run by Gazi University at 2 sites 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 4 inclusion and 8 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 16 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites 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. 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?

Range of motion (time frame: Baseline and 3 days after the 12th session (week 4)). The study lists 4 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 16 Oct 2026.

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