- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07589712
Acute Effects of Proprioceptive Neuromuscular Facilitation on Hamstring-to-Quadriceps Strength Ratio (Acute Effects)
Acute Effects of Proprioceptive Neuromuscular Facilitation and Static Stretching on Hamstring-to-Quadriceps Strength Ratio in Healthy Young Men
Study Overview
Status
Intervention / Treatment
Detailed Description
The present study investigated the acute effects of two commonly used stretching modalities-proprioceptive neuromuscular facilitation (PNF) and static stretching-on isokinetic muscle strength and hamstring-to-quadriceps (H/Q) ratios in physically active healthy young males. The study employed a randomized crossover design with repeated measures, allowing each participant to complete both experimental conditions under standardized laboratory settings.
Participants attended three sessions: a familiarization session followed by two experimental sessions separated by at least 48 hours. Each experimental session included a standardized warm-up, followed by either PNF or static stretching intervention, and subsequent isokinetic strength testing. Peak torque values for quadriceps (concentric) and hamstrings (concentric and eccentric) were measured using an isokinetic dynamometer at 60°/s. Traditional and functional H/Q ratios were calculated.
The primary aim was to determine whether these stretching modalities produce acute alterations in muscle strength and H/Q ratios. The study also examined whether the type of ratio (traditional vs. functional) significantly influences outcomes. Findings contribute to understanding the neuromuscular implications of stretching in warm-up protocols.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
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Trabzon, Ordu, Giresun, Rize, Artvin, Gümüşhane
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Gümüşhane, Trabzon, Ordu, Giresun, Rize, Artvin, Gümüşhane, Turkey (Türkiye), 29600
- Gumushane Univetsity
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age between 18 - 25 years, healthy male individuals
- Physically active (≥3 days/week, ≥30 min/day)
Exclusion Criteria:
- Musculoskeletal injury in the last 6 months
- Any neurological or orthopedic disorder
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: PNF Stretching
Participants performed four repetitions of PNF stretching consisting of a 6-second isometric hamstring contraction at approximately 60% of maximal voluntary contraction followed by a 30-second passive stretch.
Rest intervals were standardized.
|
Participants performed four repetitions of PNF stretching consisting of a 6-second isometric hamstring contraction at approximately 60% of maximal voluntary contraction followed by a 30-second passive stretch.
Rest intervals were standardized.
Participants performed four repetitions of static hamstring stretching, each lasting 30 seconds, with 30-second rest intervals between repetitions.
|
|
Experimental: Static Stretching
Participants performed four repetitions of static hamstring stretching, each lasting 30 seconds, with 30-second rest intervals between repetitions
|
Participants performed four repetitions of PNF stretching consisting of a 6-second isometric hamstring contraction at approximately 60% of maximal voluntary contraction followed by a 30-second passive stretch.
Rest intervals were standardized.
Participants performed four repetitions of static hamstring stretching, each lasting 30 seconds, with 30-second rest intervals between repetitions.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Hamstring-to-Quadriceps (H/Q) Ratio
Time Frame: Immediately after intervention
|
Both traditional (Hcon/Qcon) and functional (Hecc/Qcon) ratios were calculated using isokinetic peak torque values.
|
Immediately after intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Quadriceps Concentric Peak Torque
Time Frame: Immediately post-intervention
|
Quadriceps Concentric Peak Torque
|
Immediately post-intervention
|
|
Hamstring Concentric Peak Torque
Time Frame: Immediately post-intervention
|
Hamstring Concentric Peak Torque
|
Immediately post-intervention
|
|
Hamstring Eccentric Peak Torque
Time Frame: Immediately post-intervention
|
Hamstring Eccentric Peak Torque
|
Immediately post-intervention
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2025/169
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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