NCT07061041

Brief 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. 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
54

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jul 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 2, 2025

Completed
Same day until next milestone

Study Start

First participant enrolled

July 2, 2025

Completed
9 days until next milestone

First Posted

Study publicly available on registry

July 11, 2025

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 20, 2025

Completed
5 days until next milestone

Study Completion

Last participant's last visit for all outcomes

August 25, 2025

Completed
Last Updated

July 20, 2026

Status Verified

July 1, 2026

Enrollment Period

2 months

First QC Date

July 2, 2025

Last Update Submit

July 17, 2026

Conditions

Keywords

flexibilitystatic strechingminimal-dosehamstring flexibility

Outcome Measures

Primary Outcomes (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.

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

Study Arms (3)

Control group

NO INTERVENTION

Only tests were performed in the group, no intervention was introduced

Streching group

EXPERIMENTAL

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

Other: Streching group

Strength training group

EXPERIMENTAL

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.

Other: Strength training

Interventions

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.

Strength training group

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

Streching group

Eligibility Criteria

Age18 Years - 25 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Józef Piłsudski Academy of Physical Education in Warsaw

Warsaw, 00-968, Poland

Location

Related Publications (2)

  • 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.

    PMID: 20023343BACKGROUND
  • 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.

    PMID: 38943165BACKGROUND

MeSH Terms

Interventions

Resistance Training

Intervention Hierarchy (Ancestors)

Exercise TherapyRehabilitationAftercareContinuity of Patient CarePatient CareTherapeuticsPhysical Therapy ModalitiesPhysical Conditioning, HumanExerciseMotor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
The post-intervention measurements were conducted by an assessor who was trained in the testing procedure and blinded to group allocation, with no knowledge of whether participants belonged to the intervention or control groups.
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Laboratory Assistant

Study Record Dates

First Submitted

July 2, 2025

First Posted

July 11, 2025

Study Start

July 2, 2025

Primary Completion

August 20, 2025

Study Completion

August 25, 2025

Last Updated

July 20, 2026

Record last verified: 2026-07

Data Sharing

IPD Sharing
Will not share

Locations