- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07164729
- Original Trial
Dynamic vs. PNF Quadriceps Stretching in Cyclists
November 26, 2025 updated by: Çiçek Günday, Istinye University
Comparison of the Effects of Dynamic and PNF Stretching Applied to the Quadriceps Muscle Group on Muscle Performance, Muscle Strength, and Joint Range of Motion in Professional Cyclists
Following an initial assessment, 30 professional cyclists will be divided into two groups (1:1).
PNF stretching will be applied to the Quadriceps muscles of the participants in Group A, while Group B will perform dynamic stretching on the Quadriceps muscles.
After the interventions, all participants will undergo a second assessment.
The study aims to compare the immediate effects of these two different types of stretching on muscle performance, strength and joint range of motion.
Participants will attend a single day for both the assessments and the intervention sessions.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
30
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
-
-
-
Istanbul, Turkey (Türkiye)
- Istinye University Physiotherapy and Rehabilitation Application and Research Center (ISUFIZYOTEM)
-
-
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:
- Being a professional cyclist (training intensively at least 4-5 times per week and having a minimum of 5-10 years of cycling experience).
- Voluntary participation in the study.
- No recent history of sports-related injury.
Exclusion Criteria:
- Presence of neurological, orthopedic, or cardiovascular diseases.
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: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: PNF Stretching
|
Dynamic stretching of the quadriceps will be performed using walking lunges.
This exercise dynamically stretches the quadriceps and hip flexors while also improving balance and coordination.
During the exercise, participants stand upright, step one leg forward, and lower their body by bending the knee.
They then step forward with the other leg to complete the movement.
Ten steps will be performed for each leg.
|
|
Experimental: Dynamic Stretching
|
The "Hold-Relax" technique will be applied.
Hold-Relax PNF stretching is based on the principle of isometric contraction of the muscle followed by passive stretching.
This technique is effective for increasing muscle flexibility and reducing muscle tension.
The medial and lateral parts of the quadriceps will be stretched by Flexion-Adduction-External Rotation and Flexion-Abduction-Internal Rotation patterns3.
During the exercise, participants will lie prone with the knee flexed.
They will be asked to attempt knee extension while the movement is resisted by the physiotherapist.
The contraction will be maintained for 10 seconds, after which the participant will be instructed to relax.
Following relaxation, the knee flexion angle will be increased.
Ten repetitions will be performed for each leg.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Vertical Jump Test
Time Frame: Through study completion, an average of 1 month
|
The vertical jump test is performed by instructing an athlete to jump as high as possible from a standing position.
Typically, the athlete will first stand and reach upward to mark the highest point they can touch while standing.
Then, they will jump as high as possible, and the jump height will be recorded.
The difference between the standing reach and jump height is calculated as the vertical jump distance.
|
Through study completion, an average of 1 month
|
|
Anaerobic Power Step Test
Time Frame: Through study completion, an average of 1 month
|
It involves stepping up and down on a platform of a specified height.
The participant will step rapidly and rhythmically on the platform for 30 and 60 seconds, aiming to complete as many steps as possible.
The total number of steps will be recorded at the end of the test.
Proper form and rhythmic stepping will be emphasized during the test; the athlete must place the entire foot on the platform and achieve full extension with each step.
The data obtained from this test will be used to assess the athlete's anaerobic capacity and lower-body explosive power
|
Through study completion, an average of 1 month
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Lower Extremity Muscle Strength
Time Frame: Through study completion, an average of 1 month
|
Lower extremity muscle strength will be measured using the Lafayette Hand-Held Dynamometer (HHD).
During its application, the Lafayette HHD measures the force generated during the muscle's maximal isometric contraction.
Knee flexion, knee extension, hip flexion and hip extension muscle strength will be measured.
The measurement will be repeated three times.
|
Through study completion, an average of 1 month
|
|
Lower Extremity Joint Range of Motion
Time Frame: Through study completion, an average of 1 month
|
Lower extremity joint range of motion will be assessed using a goniometer.
The joint range of motion measurements will include hip flexion, extension, abduction, adduction, internal and external rotation, as well as knee flexion and extension.
|
Through study completion, an average of 1 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Çiçek Günday, Asst. Prof., Istinye University
- Study Chair: Arda Akça, Physiotherapist, Istinye University
- Study Chair: Elif Berfin Bulut, Physiotherapist, Istinye University
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)
September 1, 2025
Primary Completion (Actual)
October 27, 2025
Study Completion (Actual)
October 27, 2025
Study Registration Dates
First Submitted
September 2, 2025
First Submitted That Met QC Criteria
September 2, 2025
First Posted (Estimated)
September 10, 2025
Study Record Updates
Last Update Posted (Estimated)
December 3, 2025
Last Update Submitted That Met QC Criteria
November 26, 2025
Last Verified
November 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 02092025
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.
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