- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04463186
Time Based Effects of Different Duration Stretching on Calf Muscle Strength
July 8, 2020 updated by: Masood Khan, King Saud University
Time-based Effects of Different Duration Stretching on Calf Muscle Strength
Stretching is reported to decrease muscle strength and thus suggested to be avoided prior to athletic events but with conflicting reports.
This time course study aimed to assess acute effects of static stretching of different durations on isometric maximum voluntary contraction force of calf muscle.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Stretching is reported to decrease muscle strength and thus suggested to be avoided prior to athletic events but with conflicting reports.
This time course study aimed to assess acute effects of static stretching of different durations on isometric maximum voluntary contraction force of calf muscle.
Pretest posttest experimental design was used.
14 subjects participated in three experimental trials: Static stretching for 2 minutes (SS2), static stretching for 4 minutes (SS4), and static stretching for 8 minutes (SS8).
Strength was measured before (pre), immediately after (post), and at 10- and 20- minutes post stretching.
Each static stretching (SS) trial involved varied repetitions of 30-seconds self-stretches and 20-seconds relax periods.
Study Type
Interventional
Enrollment (Actual)
14
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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Riyadh, Saudi Arabia, 11433
- King Saud University
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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
24 years to 30 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Subjects performed active foot dorsiflexion in long sitting position with back supported against wall and those having not more than 20-degree range of motion were selected
- Used to engage in 1 to 5 hours of physical activity per week
Exclusion Criteria:
- Subjects having any current injury or limits in range of motion specific to lower limb joints
- Current neuromuscular disease
- Competitive athletes were excluded from the study
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: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Experimental
subjects participated in three experimental trials: Static stretching for 2 minutes (SS2), static stretching for 4 minutes (SS4), and static stretching for 8 minutes (SS8).
Strength was measured before (pre), immediately after (post), and at 10- and 20- minutes post stretching.
|
Static stretching for 2 minutes (SS2), static stretching for 4 minutes (SS4), and static stretching for 8 minutes (SS8).
Each static stretching (SS) trial involved varied repetitions of 30-seconds self-stretches and 20-seconds relax periods.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in Isometric Maximum Voluntary Contraction Force
Time Frame: MVCF at baseline and 0, 10, 20-min post stretching
|
Isometric Maximum Voluntary Contraction Force was measured using strain Gauge.
|
MVCF at baseline and 0, 10, 20-min post stretching
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
January 30, 2019
Primary Completion (Actual)
August 13, 2019
Study Completion (Actual)
August 29, 2019
Study Registration Dates
First Submitted
July 5, 2020
First Submitted That Met QC Criteria
July 8, 2020
First Posted (Actual)
July 9, 2020
Study Record Updates
Last Update Posted (Actual)
July 9, 2020
Last Update Submitted That Met QC Criteria
July 8, 2020
Last Verified
July 1, 2020
More Information
Terms related to this study
Other Study ID Numbers
- RRC-2019-05
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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