- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06469346
Comparison of Eccentric Exercise and Static Stretching on Muscle Flexibility (COEESS)
Comparison Between Eccentric Exercise and Static Stretching on Hamstring Muscle Flexibility in Healthy Young
Background: Muscle flexibility is a fundamental physical quality for body development, daily life and sports activities, and also for maintaining muscle quality during aging. Limited flexibility leads to an increased prevalence of musculoskeletal injury in general population and longer return to sports activities.
Among the existent strategies to increase muscle flexibility in sports training and physical rehabilitation, static stretching is commonly used by health and physical activity professionals. Its effectiveness in increasing flexibility has been widely demonstrated; however its effects on muscle strength and power remains controversial.
Therefore, eccentric resistance exercise has been proposed as an effective intervention for increasing muscle flexibility through structural changes on muscle architecture (pennation angle and fascicle length) with the additional benefit of resistance training on muscle strength and power. Nonetheless, its unknown if the increase in muscle flexibility through eccentric resistance exercise could be similar to what has been previously demonstrated with static stretching.
Study Overview
Status
Detailed Description
Hypothesis: The increase in hamstring flexibility after 6 weeks of eccentric resistance training in young males would be similar compared to 6 weeks static stretching training in the same population.
Goals: The primary aim of the study is to compare the effectiveness of 6 weeks eccentric resistance training vs 6 weeks static stretching training on hamstring flexibility in young males.
Specific Goals: Determine the effect of 6 weeks excentric exercise training and 6 weeks static stretching training on unilateral maximal isometric voluntary strength between both groups
To compare the effect of 6 weeks excentric exercise training and 6 weeks static stretching training in structural changes on muscle architecture (pennation angle, fascicle length and muscle thickness).
Methodology:
Study design: Forty two young males between 18 and 35 years will be divided into three groups: hamstring eccentric resistance training group (EEG, n=14), hamstring static stretching group (SSG, n=14) and control group (CG, n=14). Volunteers of eccentric resistance training group will be subjected to 6 weeks of Nordic hamstring exercise (3x/wk), while volunteers of static stretching group will be subjected to 6 weeks of hamstring passive static stretching (3x/wk). Control group will not attend any type of intervention. Before and after 6 weeks of training, Knee Extension Angle and Sit and Reach test will be performed for measuring hamstring flexibility. Unilateral Hamstring Isometric Maximal Voluntary Strength will be determined by load cell force transducer, and pennation angle, fascicle length and muscle thickness of Long Head Biceps Femoris will be conducted through muscle ultrasonography
Study parameters/endpoint:
The main study endpoint is the increase in hamstring flexibility assessed with Knee Extension Angle and Sit and Reach Test.
Secondary endpoints include Unilateral Hamstring Isometric Maximal Voluntary Strength (IMVS) and Architectural changes in Long Head Biceps Femoris muscle.
Other parameters include age, body weight, body height, body mass index (BMI), level of physical activity.
Expected results: With the proposed project, the investigators expect that eccentric exercise training will increase hamstring muscle flexibility at similar level compared with static stretching training. The findings will define the potential of eccentric exercise training on muscle flexibility in healthy participants. These results could expand the benefits of this type of exercise training focused on being included in populations with limited mobility such as elderly and injured populations
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Cautín
-
Temuco, Cautín, Chile, 4780000
- Universidad de La Frontera
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Masculine University students between 18 and 35 years old
- Physically Inactive considering physical activity recommendations from World Health Organization
- Bilateral hamstring muscle stiffness defined as <160° in passive Knee Extension Angle Test
- Body Max Index 18,5 < BMI < 24,9 kg/m2
Exclusion Criteria:
- Lower back and lower limb (hip, thigh, knee, ankle) musculoskeletal injury in the last 12 months.
- Hamstring injury (strain, tendinopathy, tendon avulsion) previously during the period of life
- Dietary anabolic supplements consumption
- Musculoskeletal, cardiovascular, respiratory o similar health condition that limits participation on physical activity programs
- Regular resistance training (2 or more times per week, carrying out progressive training) in the previous 6 months
- Smoker (1 cigarette per day)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Eccentric Exercise Group (EEG)
These participants will be subjected to 6 weeks of Nordic hamstring eccentric exercise (3 times per week)
|
Warm up: stationary bycicle at 50 watts and 60 bpm Mobility exercises for hip and knee joint Nordic eccentric exercise protocol:
|
|
Experimental: Static Stretching Group (SSG)
These participants will be subjected to 6 weeks of passive static stretching on hamstring muscle (3 times per week)
|
Warm up: stationary bycicle at 50 watts and 60 bpm Mobility exercises for hip and knee joint
|
|
Other: Control Group
These participants will not be under any type of treatment during the intervention protocol
|
No intervention
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knee Extension Angle
Time Frame: Before and after 6 weeks of training
|
The degree changes in passive knee extension will be assessed using Passive Knee Extension Angle Test after intervention
|
Before and after 6 weeks of training
|
|
Sit-and-Reach
Time Frame: Before and after 6 weeks of training
|
The distance (in centimeters) of change on functional posterior chain flexibility will be obtained in Sit-and-Reach Test after intervention
|
Before and after 6 weeks of training
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Maximal Isometric Voluntary Strength
Time Frame: Before and after 6 weeks of training
|
Change in unilateral isometric hamstring strength will be evaluated with load cell force transducer after intervention
|
Before and after 6 weeks of training
|
|
Long Head Biceps Femoris Pennation Angle
Time Frame: Before and after 6 weeks of training
|
Change in pennation angle will be measured using muscular ultrasound after intervention
|
Before and after 6 weeks of training
|
|
Long Head Biceps Femoris Fascicle Length
Time Frame: Before and after 6 weeks of training
|
Change in fascicle length will be measured using muscular ultrasound after intervention
|
Before and after 6 weeks of training
|
|
Long Head Biceps Femoris Muscle Thickness
Time Frame: Before and after 6 weeks of training
|
Change in muscle thickness will be measured using muscular ultrasound after intervention
|
Before and after 6 weeks of training
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Gabriel N Marzuca-Nassr, Universidad de La Frontera
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Other Study ID Numbers
- MGTFNG-2024
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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