Personalized Recommendation System for Sport Activities

April 17, 2024 updated by: Juan López Barreiro, University of Vigo

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

Active, not recruiting

Conditions

Study Type

Interventional

Enrollment (Actual)

47

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

      • Pontevedra, Spain, 36005
        • University of Vigo
        • Contact:
        • 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

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:

  • 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

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: 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

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

April 15, 2024

Primary Completion (Estimated)

June 15, 2024

Study Completion (Estimated)

July 15, 2024

Study Registration Dates

First Submitted

December 27, 2023

First Submitted That Met QC Criteria

January 9, 2024

First Posted (Actual)

January 11, 2024

Study Record Updates

Last Update Posted (Actual)

April 18, 2024

Last Update Submitted That Met QC Criteria

April 17, 2024

Last Verified

April 1, 2024

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

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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