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FlexibilityNCT07061041

Comparison of the Effects of Static Stretching and Full Range of Motion Strength Training on Posterior Band Flexibility

A study testing Strength training and Streching group in people with Flexibility and Strength Training Effects, run by Józef Piłsudski University of Physical Education at 1 site in Poland.

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 study will be conducted in 2025. The methods used in the study are non-invasive methods. One study group will perform 2 series of static stretching of the posterior band once a week. The stretching time in each series will be 60s, and the duration of the intervention will be 6 weeks. Read more about this study

Who is it for?
Ages 18 to 25 yearsHealthy volunteers can take part
What is being tested?
Strength training and Streching group
Could I receive a placebo?
No, everyone receives an active treatment
How many people
54 participants
Where
1 sitePoland
Study dates
2 Jul 2025to 25 Aug 2025
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 25 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Participants were required to be ≥18 years of age and free from musculoskeletal injuries or surgical procedures involving the lower extremities or trunk within the previous six months.

Who cannot join

  • Participants were excluded if they were <18 years of age or had sustained a musculoskeletal injury or undergone surgery involving the lower extremities or trunk within the previous six months.

Trial locations and contacts

1 site in 1 country.

Poland1 site
  • Józef Piłsudski Academy of Physical Education in Warsaw

    Warsaw, 00-968

Other trials in Poland

About this study

The study will be conducted in 2025. The methods used in the study are non-invasive methods. One study group will perform 2 series of static stretching of the posterior band once a week. The stretching time in each series will be 60s, and the duration of the intervention will be 6 weeks. The test subjects will maintain a maximum prone position with their knee joints straight for a specified period of time during the stretching. The second study group will perform full range of motion strength training in the form of 3 series of 10 repetitions of the Romanian Deadlift (RDL) once a week, with the intervention duration also being 6 weeks. Prior to the start of the study, participants will undergo a toe-to-floor test to assess posterior band flexibility. The test will be repeated again after the intervention.

Being tested
Strength training, Streching group
Keywords
flexibility, static streching, minimal-dose, hamstring flexibility

What participants receive

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

  • Strength trainingOther

    The group will perform one workout per week consisting of 3 series of the "Romanian deadlift" exercise of 10 repetitions. Each repetition will be performed at a specific pace - 3s in eccentric contraction and 1s in concentric contraction. The aforementioned exercise, the Romanian deadlift, will be performed by the subjects on a platform (elevation) in order to achieve maximum range of motion.

  • Streching groupOther

    The group performed one training session per week consisting of 2 sets of 60 seconds of static stretching

Study groups in NCT07061041
Study groupRoleWhat they receive
Control groupNo interventionOnly tests were performed in the group, no intervention was introduced
Streching groupExperimentalThe group performed one training session per week consisting of 2 sets of 60 seconds of static stretching
Receives: Other: Streching group
Strength training groupExperimentalThe group will perform one workout per week consisting of 3 series of the "Romanian deadlift" exercise of 10 repetitions. Each repetition will be performed at a specific pace - 3s in eccentric contraction and 1s in concentric contraction. The aforementioned exercise, the Romanian deadlift, will be performed by the subjects on a platform (elevation) in order to achieve maximum range of motion.
Receives: Other: Strength training

What is being measured

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

  1. Flexibility

    Flexibility was assessed using a modified stand-and-reach test. The participants stood with their feet shoulder-width apart and knees fully extended, then performed a forward bend, reaching as far as possible while maintaining straight legs. To measure the extent of their reach, a custom-built box was used. The box had the following dimensions: a length of 40 cm, a width of 45 cm, and a height of 35 cm. Each participant performed two trials, and the mean value was used for statistical analysis.. The same test was repeated after the 6-week intervention period to determine any improvements in flexibility.

    Measured: From registration to completion of the study, the duration is up to 8 weeks

Timeline

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

  1. First posted11 Jul 2025
  2. Study start2 Jul 2025
  3. Primary completion20 Aug 2025
  4. Study completion25 Aug 2025

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
Other
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
54 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07061041
Sponsor's protocol ID
SKE.0030.59.2025
Status last verified
Jul 2026
First submitted
2 Jul 2025
Last updated
20 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Shadmehr A, Hadian MR, Naiemi SS, Jalaie S. Hamstring flexibility in young women following passive stretch and muscle energy technique. J Back Musculoskelet Rehabil. 2009;22(3):143-8. doi: 10.3233/BMR-2009-0227.

    PubMed 20023343
  • Rosenfeldt M, Stien N, Behm DG, Saeterbakken AH, Andersen V. Comparison of resistance training vs static stretching on flexibility and maximal strength in healthy physically active adults, a randomized controlled trial. BMC Sports Sci Med Rehabil. 2024 Jun 28;16(1):142. doi: 10.1186/s13102-024-00934-1.

    PubMed 38943165

Questions about this trial

What is this clinical trial studying?

A study testing Strength training and Streching group in people with Flexibility and Strength Training Effects, run by Józef Piłsudski University of Physical Education at 1 site in Poland.

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 1 inclusion and 1 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 20 Jul 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 Poland. 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?

Flexibility (time frame: From registration to completion of the study, the duration is up to 8 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07061041, which also lists 2 linked publications.

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 20 Jul 2026.

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