- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06200350
Personalized Recommendation System for Sport Activities
Personalized Recommendation System of Specific Challenges for Sport Activities: Practical Approach to Football
The goal of this clinical trial is to test and compare the effects of a tailored algorithm recommendation of sport activities concreted in challenges to improve some critical performance dimensions.
Q1: Improving participant performance is achieved by using personalized sports activity recommendation using an algorithm and tracking compliance using a decentralized application (dApp)? Q2: Are participants satisfied with the performance and simplicity of the dApp used?
Participants will be asked to do specific activities recommended by the developed recommender system. The activities to be carried out will be conditioned by the profile obtained from each participant at the beginning of the intervention. They will consist of reinforcement activities for the dimensions with the lowest scores.
Researchers will compare a experimental group and a control group to see if the dimensions assessed at the beginning of the intervention were improved.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Pontevedra, Spain, 36005
- University of Vigo
-
Contact:
- Juan López-Barreiro, BsC
- Phone Number: 610669712
- Email: juan.lopez.barreiro@uvigo.gal
-
Principal Investigator:
- Juan López-Barreiro, BsC
-
Principal Investigator:
- Jose Luis García-Soidán, PhD
-
Principal Investigator:
- Luis Álvarez-Sabucedo, PhD
-
Principal Investigator:
- Juan-Manuel Santos-Gago, PhD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Amateur football players.
- Aged between 14 and 18 years old.
- Without any injury.
- The ones who can attend the assessing sessions and fill in the informed consent form.
Exclusion Criteria:
- Aged different from the indicated above.
- Injured.
- Missing one of the assessing sessions.
- Not performing the proposed training twice, or not registering two or more training sessions.
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: Experimental group
This group will carry out the tailored training proposed by de recommender system, and followed and encouraged by the blockchain dApp.
|
Tailored training based on the profile of each participant.
|
Active Comparator: Control group
This group will continue with the traditional training planned.
|
They will continue with the traditional training.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Score of the system usability at the end of the intervention
Time Frame: At the end of the intervention (8 weeks)
|
System Usability Scale is a scale from 0 to 100 points to assess the usability of the system used in the intervention.
|
At the end of the intervention (8 weeks)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Squat Jump (SJ)
Time Frame: At baseline and after 8 weeks
|
Lower body capacity assessed using the SJ
|
At baseline and after 8 weeks
|
Abdominal planck (AP)
Time Frame: At baseline and after 8 weeks
|
Core capacity assessed using the abdominal plank lasting time
|
At baseline and after 8 weeks
|
Push ups (PU)
Time Frame: At baseline and after 8 weeks
|
Upper body capacity assessed using the number of pushups performed in one minute
|
At baseline and after 8 weeks
|
Cooper Test (GE)
Time Frame: At baseline and after 8 weeks
|
General endurance assessed using the Cooper Test
|
At baseline and after 8 weeks
|
15m sprint (SE-15)
Time Frame: At baseline and after 8 weeks
|
Special endurance assessed using the 15m sprint
|
At baseline and after 8 weeks
|
Countermovement Jump (CMJ)
Time Frame: At baseline and after 8 weeks
|
Special endurance assessed using the CMJ
|
At baseline and after 8 weeks
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Sociodemographic outcomes
Time Frame: At baseline
|
Body weight, height, age and gender.
|
At baseline
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
- 09-181223
- ED481A-2021/350 (Other Grant/Funding Number: Xunta de Galicia)
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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