- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04453644
Effects of Stretching on Strength of Proximal and Distal Group of Muscles - A Comparative Study
Study Overview
Detailed Description
OBJECTIVE: To compare the effects of 2, 4, and 8 min of static stretching (SS) on isometric maximum voluntary contraction (MVCF) force between proximal (Hamstrings) and distal group (Calf) of muscles.
DESIGN: Two-group pretest-posttest experimental design. METHODS: Each subject visited the Rehabilitation center on three days: On day-I for static stretching for 2 minutes (SS2), day-II for 4 minutes (SS4), and day-III for 8 minutes (SS8). Isometric Maximum Voluntary Contraction Force (MVCF) measurement was done prior (Pre), 0-min, 10-min, and 20-min post-intervention (i.e. stretching). Each visit was separated by a gap of at least 3-4 days. On each visit, each subject underwent (a). Pre-intervention evaluation, (b). Intervention, (c). Post-intervention evaluation. Subjects performed stretching exercises under the supervision of expert Physical Therapist. The outcome assessor who was kept blind to study protocol did all measurements.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Riyadh, Saudi Arabia, 11433
- King Saud University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
For group A: subjects performed active knee extension test and those lacking at least 20 degrees of active knee extension range, with hip in 90 degree of flexion were selected. For group B (Calf): Subjects performed active foot dorsiflexion in long sitting position with back supported against the wall and those having not more than 20-degree range of motion were selected.
Selected subjects used to engage in 1-5 hours of regular physical activity per week (recreationally active) that does not involve stretching exercise
Exclusion Criteria:
Subjects reporting any current or ongoing neuromuscular disease, injury specific to lower limb joints, any apparent limit in knee or ankle ROM and competitive/professional athletes were excluded from study.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Group A (Hamstrings)
Hamstring stretching would be done then isometric strength would be measured.
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On day-I: Static Stretching done for 2 minutes (SS2), on day-II: Static Stretching done for 4 minutes (SS4), and on day-III: Static Stretching done for 8 minutes (SS8).
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Experimental: Group B (Calf)
Calf stretching would be done then isometric strength would be measured.
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On day-I: Static Stretching done for 2 minutes (SS2), on day-II: Static Stretching done for 4 minutes (SS4), and on day-III: Static Stretching done for 8 minutes (SS8).
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in isometric maximum voluntary contraction force before and after stretching
Time Frame: MVCF was measured immediately (0 min), 10-min and 20 min post intervention on 3 different days, with each day separated by gap of 3-4 days.
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Change in isometric muscle strength measured before and after stretching using strain gauge on 3 different days
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MVCF was measured immediately (0 min), 10-min and 20 min post intervention on 3 different days, with each day separated by gap of 3-4 days.
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Collaborators and Investigators
Sponsor
Publications and helpful links
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
Other Study ID Numbers
- RRC-2019-06
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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