The Influence of Acute Static Stretching on the Ankle Joint-position Sense of Soccer Players

April 7, 2024 updated by: University Fernando Pessoa

The Influence of Acute Static Stretching on the Ankle Joint-position Sense of Soccer Players: a Randomized Controlled Trial

The aim of this study isto investigate the influence of acute static stretching on the ankle joint position sense of soccer players.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

This crossover randomized controlled trial will include semi-professional soccer players. All participants will perform 3 conditions: two experimental conditions, of static stretching of the gastrocnemius and tibialis anterior muscles, for 30 seconds or 90 seconds; and a control condition (rest). Ankle joint position sense of the dominant limb will be assessed before and immediately after the conditions for the range of 20º of plantar flexion by active repositioning, and using a video camera. Absolute, relative and variable angular errors will be calculated.

Study Type

Interventional

Enrollment (Actual)

19

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 Contact

Study Locations

      • Porto, Portugal, 4200-253
        • Escola Superior de Saúde Fernando Pessoa

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • male soccer players from the senior level
  • aged between 18 and 30 years old
  • with normal plantar flexion range of motion
  • without history of lower limb injuries in the last 6 months

Exclusion Criteria:

  • those with cardiorespiratory, vestibular or neurological diseases
  • with bone or joint deformities in the lower limb
  • cerebral concussion in the last 3 months
  • history of lower limb surgery
  • those with positive ankle integrity tests (anterior drawer test, talus tilt test and external rotation stress test)

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: Health Services Research
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control Condition
5-minute rest
Active Comparator: Static Stretching of 30 seconds Condition
Static stretching of the gastrocnemius and tibialis anterior muscles for 30 seconds

The static stretching protocol will include the following muscle groups of the dominant lower limb:

  • Gastrocnemius - Participants will assume a bipedal position facing a wall. Then, the leg that is not being stretched will be placed forward, with the knee in semi-flexion, and the leg that is being stretched, behind, with the knee in full extension. Instructions will be given in order to keep the calcaneus on the floor;
  • Tibialis anterior - Participants will be facing a wall, with the entire foot in touch with the ground and toes pointing forward. Then, they will secure themselves to a handrail and project the hips back.

These stretchings will be held in a position where the participants refer discomfort, and will be maintained for 30 seconds or 90 seconds according to the condition.

Active Comparator: Static Stretching of 90 seconds Condition
Static stretching of the gastrocnemius and tibialis anterior muscles for 90 seconds

The static stretching protocol will include the following muscle groups of the dominant lower limb:

  • Gastrocnemius - Participants will assume a bipedal position facing a wall. Then, the leg that is not being stretched will be placed forward, with the knee in semi-flexion, and the leg that is being stretched, behind, with the knee in full extension. Instructions will be given in order to keep the calcaneus on the floor;
  • Tibialis anterior - Participants will be facing a wall, with the entire foot in touch with the ground and toes pointing forward. Then, they will secure themselves to a handrail and project the hips back.

These stretchings will be held in a position where the participants refer discomfort, and will be maintained for 30 seconds or 90 seconds according to the condition.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Absolute angular error
Time Frame: Change from Baseline (Before) to Immediately after interventions or control (After)
The absolute value of the difference between the target range and the achieved range
Change from Baseline (Before) to Immediately after interventions or control (After)
Relative angular error
Time Frame: Change from Baseline (Before) to Immediately after interventions or control (After)
The arithmetic difference between the target range and the range achieved
Change from Baseline (Before) to Immediately after interventions or control (After)
Variable angular error
Time Frame: Change from Baseline (Before) to Immediately after interventions or control (After)
The standard deviation of the 3 repositionings
Change from Baseline (Before) to Immediately after interventions or control (After)

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Joana Azevedo, PhD, Escola Superior de Saúde Fernando Pessoa

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)

February 12, 2024

Primary Completion (Actual)

March 13, 2024

Study Completion (Actual)

March 29, 2024

Study Registration Dates

First Submitted

March 13, 2024

First Submitted That Met QC Criteria

March 13, 2024

First Posted (Actual)

March 20, 2024

Study Record Updates

Last Update Posted (Actual)

April 9, 2024

Last Update Submitted That Met QC Criteria

April 7, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • ESS/FSA-397/23-2

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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