Effects of Stretching on Strength of Proximal and Distal Group of Muscles - A Comparative Study

June 28, 2020 updated by: Masood Khan, King Saud University
Muscular flexibility is believed to prevent injuries and improve movement therefore most coaches include stretching exercises in their pre-competition and pre-exercise warm-up routines. One question arises here, should sports persons avoid stretching exercises prior to sporting events thereby exposing themselves to musculoskeletal injuries, or should they continue stretching exercises prior to sporting events and risk losing the maximal performance? The aim of this study is 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.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

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

Interventional

Enrollment (Actual)

28

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

      • Riyadh, Saudi Arabia, 11433
        • King Saud University

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

22 years to 30 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

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

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: 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.
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).
Experimental: Group B (Calf)
Calf stretching would be done then isometric strength would be measured.
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).

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.
Change in isometric muscle strength measured before and after stretching using strain gauge on 3 different days
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.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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 23, 2019

Primary Completion (Actual)

July 17, 2019

Study Completion (Actual)

September 5, 2019

Study Registration Dates

First Submitted

June 24, 2020

First Submitted That Met QC Criteria

June 28, 2020

First Posted (Actual)

July 1, 2020

Study Record Updates

Last Update Posted (Actual)

July 1, 2020

Last Update Submitted That Met QC Criteria

June 28, 2020

Last Verified

June 1, 2020

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)?

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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