Motivation as a Strategy for Adherence to a Stretching Program for Basketball Players (MOTBAS)

November 25, 2022 updated by: CRISTINA ADILLÓN, University Rovira i Virgili

Motivation as a Strategy for Adherence to a Stretching Program for Basketball Players: a Pilot Study.

Background: Basketball is considered a medium-high injury sport, because of the mechanisms of injury, which can be acute, by repetition mechanisms or by overload. An effective way to avoid muscle overload injuries is to perform an extensibility workout such as an analytical active stretching program. The objective of this study is to achieve adherence to a stretching program by motivating young basketball players.

Methods: Randomized experimental clinical trial controlled by a single blind person. 21 child players between 11 and 12 years, divided into intervention group (IG) and control group (CG). IG carries out a supervised static stretching program at the end of training 3 days/week for 12 weeks and CG has normally developed the standard stretches of their Basketball Club. The extensibility of various muscle groups was valued in both groups. In addition, motivation was valued by Sport Motivation Scale.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

The inclusion criteria were: to be between 12 and 13 years of age (both included), to be an active player at the time of selection, to sign the informed consent form and failure to meet the exclusion criteria. The exclusion criteria were: to have an injury at the time of selection and psychological and/or psychiatric illnesses. The main outcomes were: the adherence to a stretching program (monitoring calendars), the extensibility of the posterior musculature (fingertip-to-floor test), the adductor extensibility (sideways leg splits test), the gastrocnemius and soleus extensibility (weight-bearing lunge test through the Leg Motion system), the hamstring extensibility (goniometer with the passive straight leg raise and it was considerated shortening if it doesn't reach >80 degrees of elevation, the extensibility of the quadriceps (Ely test by a goniometer), the extensibility of the psoas (modified Thomas test using a goniometer).

Study Type

Interventional

Enrollment (Actual)

21

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

      • Barcelona, Spain, 08018
        • Federación Catalana de Baloncesto

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

12 years to 13 years (CHILD)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • To be an active player at the time of selection, to sign the informed consent form, failure to meet the exclusion criteria.

Exclusion Criteria:

  • To have an injury at the time of selection, psychological and/or psychiatric illnesses.

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: PREVENTION
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Experimental group
The experimental group received a lecture session explaining what stretching is, its advantages and the importance of stretching in injury prevention. The specific intervention programme was to be performed at least 3 days/week (after training) for 12 weeks. These were static, active stretches of the muscles of the lower back, psoas iliacus, quadriceps, adductors, gluteus, hamstrings, and sural triceps. For each muscle group, the stretch was held for 60 seconds, divided into 3 repetitions of 20 seconds. Between each repetition, we did not return to the initial position but sought a new barrier to the stretch which would provoke the sensations described above. The total time dedicated to stretching was approximately 15 minutes per session.
The stretching programme was to be performed at least 3 days/week (after training) for 12 weeks. These were static, active stretches of the muscles of the lower back, psoas iliacus, quadriceps, adductors, gluteus, hamstrings, and sural triceps. The final stretching position was that which generated a sensation of moderate-intense tightness in the muscles, but without exceeding the pain threshold. For each muscle group, the stretch was held for 60 seconds, divided into 3 repetitions of 20 seconds. Between each repetition, we did not return to the initial position but sought a new barrier to the stretch which would provoke the sensations described above. The total time dedicated to stretching was approximately 15 minutes per session.
NO_INTERVENTION: Control group
The control group performed the initial and final assessments and continued to perform their team's standard/habitual stretches. To record whether they performed the stretches prescribed by the club, the researchers went to the end of the training unknown sessions and recorded whether the players performed them or not.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Extensibility of the posterior musculature (centimeters)
Time Frame: 1 year
This was measured with the "Fingertip-to-Floor Test"
1 year
Adductor extensibility (centimeters)
Time Frame: 1 year
It was measured with the Sideways Leg Splits test
1 year
Gastrocnemius and soleus extensibility (centimeters)
Time Frame: 1 year
The Leg Motion System was used.
1 year
Hamstring extensibility (degrees)
Time Frame: 1 year
The Passive Straight Leg Raise test was used, assessed qualitatively and quantitatively.
1 year
Extensibility of the quadriceps (degrees)
Time Frame: 1 year
This was measured with the Ely Test
1 year
Extensibility of the psoas (degrees)
Time Frame: 1 year
The Modified Thomas test was used, assessing the psoas qualitatively and quantitatively as well as indirectly the rectus femoris, the tensor fascia lata and the abductors.
1 year
Motivation
Time Frame: 1 year
It was assessed using the Sport Motivation Scale, validated in Spanish. This scale allows an objective assessment of the intrinsic, extrinsic and non-motivational factors of why children participate in their sport. In addition, the researchers added two questions related to motivation and stretching, to check whether the participants had correctly understood the importance of stretching.
1 year
Adherence to the programme (percentage)
Time Frame: 1 year
This was assessed by means of monitoring calendars. The purpose of these was for the athletes to place blue stickers on the days they did the stretches and red stickers on the days they did not do them, thus giving them visual biofeedback of their involvement with the stretches. Each calendar was valid for six weeks, so one was given out on the first week and the second one in the middle of the study, on the sixth week.
1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Age
Time Frame: 1 year
Years
1 year
Height
Time Frame: 1 year
Centimeters
1 year
Gender
Time Frame: 1 year
Female or male
1 year
Hypermobility
Time Frame: 1 year
The Beighton Criteria were used.
1 year

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)

September 1, 2019

Primary Completion (ACTUAL)

May 27, 2020

Study Completion (ACTUAL)

June 30, 2020

Study Registration Dates

First Submitted

August 8, 2022

First Submitted That Met QC Criteria

August 10, 2022

First Posted (ACTUAL)

August 12, 2022

Study Record Updates

Last Update Posted (ACTUAL)

November 30, 2022

Last Update Submitted That Met QC Criteria

November 25, 2022

Last Verified

November 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 123/2018_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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