- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07061041
- Original Trial
Comparison of the Effects of Static Stretching and Full Range of Motion Strength Training on Posterior Band Flexibility
July 17, 2026 updated by: Michał Kaczorowski, Józef Piłsudski University of Physical Education
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.
Study Overview
Status
Completed
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
54
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
-
-
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Warsaw, Poland, 00-968
- Józef Piłsudski Academy of Physical Education in Warsaw
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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:
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.
Exclusion Criteria:
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.
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: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control group
Only tests were performed in the group, no intervention was introduced
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Experimental: Streching group
The group performed one training session per week consisting of 2 sets of 60 seconds of static stretching
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The group performed one training session per week consisting of 2 sets of 60 seconds of static stretching
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Experimental: Strength training group
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.
|
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.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Flexibility
Time Frame: From registration to completion of the study, the duration is up to 8 weeks
|
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.
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From registration to completion of the study, the duration is up to 8 weeks
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General 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.
- 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.
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)
July 2, 2025
Primary Completion (Actual)
August 20, 2025
Study Completion (Actual)
August 25, 2025
Study Registration Dates
First Submitted
July 2, 2025
First Submitted That Met QC Criteria
July 2, 2025
First Posted (Actual)
July 11, 2025
Study Record Updates
Last Update Posted (Actual)
July 20, 2026
Last Update Submitted That Met QC Criteria
July 17, 2026
Last Verified
July 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SKE.0030.59.2025
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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.