- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07648186
Preventive Exercise Program for Adolescent Futsal Players. (INSPIRE)
June 9, 2026 updated by: Laura Ramírez Pérez, University of Malaga
Effect of a Preventive Exercise Progam on Lower-limb Injuries in Adolescent Futsal Players: a Randomized Controlled Trial.
The main aim of this study is to analyse the effect of a preventive exercise program (INSPIRE: Indoor Sports Injury Prevention) on the lower-limb injuries in adolescent futsal players.
For this purpose, 26 adolescent futsal players will be recruited, and after baseline evaluation, they will be randomized either the standard care, that will undergo the standard strengthening program developed each year in their team, or the experimental group, that will undergo the INSPIRE program, based on three stages (motor control, strength and endurance, and propioception and neural workout).
Both groups will develop a 8-week intervention.
Regarding the evaluation, the participants will have three evaluations: baseline, 4 weeks, and 8 weeks, and they will complete validated questionnaries (Overuse Injury Questionnaire, and Return to Play Score), together with functional tests (Y-Balance Test), strength testing using a dynamometer, and motor control testing using force plates.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
26
Phase
- Not Applicable
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
- Child
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Male futsal players.
- Age between 15 and 18 years.
- Players who have a confirmed team for all the season.
- Signed informed consent.
Exclusion Criteria:
- Cultural, ethical or language barrier.
- Goalkeepers.
- Participants with other diseases.
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 Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Standard Care Group
Standard strengthening program developed in Spanish futsal teams
|
Standard Strengthening Program
|
|
Experimental: INSPIRE (Indoor Sports Injury Prevention)
Exercise program based in three stages: 1. Motor control and motor relearning: based on basic movement patterns and muscle chains, together with selective activation of muscles such as gluteus, aductors, hamstrings, quadricepts, gastrocnemius, and peroneus, using closed kinetic chain exercises.
2. Strength and endurance: based on strengthening the aforementioned muscles, using pushing and reception exercises, together with long efforts.
3. Propioception and neural workout: based on the training on propioception in stable and unstable surfaces, together with exercise of acceleration, decceleration, direction changes, and dual tasks.
|
INSPIRE PROGRAM.
Exercise program based in three stages: 1. Motor control and motor relearning: based on basic movement patterns and muscle chains, together with selective activation of muscles such as gluteus, aductors, hamstrings, quadricepts, gastrocnemius, and peroneus, using closed kinetic chain exercises.
2. Strength and endurance: based on strengthening the aforementioned muscles, using pushing and reception exercises, together with long efforts.
3. Propioception and neural workout: based on the training on propioception in stable and unstable surfaces, together with exercise of acceleration, decceleration, direction changes, and dual tasks.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
OSTRC
Time Frame: Baseline, 4 weeks, 8 weeks
|
Overuse Injury Questionnaire
|
Baseline, 4 weeks, 8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
RTP
Time Frame: Baseline, 4 weeks, 8 weeks
|
Return to Play Questionnaire
|
Baseline, 4 weeks, 8 weeks
|
|
Y-Balance Test
Time Frame: Baseline, 4 weeks, 8 weeks
|
Y-Balance Test distance composite score, and asimmetry
|
Baseline, 4 weeks, 8 weeks
|
|
STRENGTH
Time Frame: Baseline, 4 weeks, 8 weeks
|
Peak force, time to peak force, rate of force development, percentage of force losing, and assimmetry using a dynamometer
|
Baseline, 4 weeks, 8 weeks
|
|
MOTOR CONTROL
Time Frame: Baseline, 4 weeks, 8 weeks
|
Ground reaction force, and centre of pressure displacement during jumps using force plates
|
Baseline, 4 weeks, 8 weeks
|
|
INJURIES
Time Frame: Baseline, 4 weeks, 8 weeks
|
Number of injuries, severity, recurrence rate, injury burden
|
Baseline, 4 weeks, 8 weeks
|
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 (Estimated)
September 1, 2026
Primary Completion (Estimated)
April 15, 2027
Study Completion (Estimated)
June 15, 2027
Study Registration Dates
First Submitted
June 9, 2026
First Submitted That Met QC Criteria
June 9, 2026
First Posted (Actual)
June 15, 2026
Study Record Updates
Last Update Posted (Actual)
June 15, 2026
Last Update Submitted That Met QC Criteria
June 9, 2026
Last Verified
June 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 170/2026
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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