Personalized Recommendation System for Sport Activities

Health Behavior Clinical Trial

Official title:

Personalized Recommendation System of Specific Challenges for Sport Activities: Practical Approach to Football

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT06200350
• Other study ID #: 09-181223
• Secondary ID: ED481A-2021/350
• Status: Active, not recruiting
• Phase: N/A
• Start date: April 15, 2024
• Est. completion date: July 15, 2024

Study information

• Verified date: April 2024
• Source: University of Vigo
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 47
• Est. completion date: July 15, 2024
• Est. primary completion date: June 15, 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 14 Years to 18 Years

Eligibility

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.

Related Conditions & MeSH terms

• Health Behavior

Intervention

Other:
• Experimental group
Tailored training based on the profile of each participant.
• Control group
They will continue with the traditional training.

Locations

Country	Name	City	State
Spain	University of Vigo	Pontevedra

Sponsors (1)

Lead Sponsor	Collaborator
University of Vigo

Country where clinical trial is conducted

Spain, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Sociodemographic outcomes	Body weight, height, age and gender.	At baseline
Primary	Score of the system usability at the end of the intervention	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	Squat Jump (SJ)	Lower body capacity assessed using the SJ	At baseline and after 8 weeks
Secondary	Abdominal planck (AP)	Core capacity assessed using the abdominal plank lasting time	At baseline and after 8 weeks
Secondary	Push ups (PU)	Upper body capacity assessed using the number of pushups performed in one minute	At baseline and after 8 weeks
Secondary	Cooper Test (GE)	General endurance assessed using the Cooper Test	At baseline and after 8 weeks
Secondary	15m sprint (SE-15)	Special endurance assessed using the 15m sprint	At baseline and after 8 weeks
Secondary	Countermovement Jump (CMJ)	Special endurance assessed using the CMJ	At baseline and after 8 weeks