Gamified Family-based Health Exercise Intervention to Improve Adherence to 24-h Movement Behaviors Recommendations in Children. (Move On)

February 28, 2025 updated by: Universidad Pública de Navarra

Gamified Exercise Intervention to Improve Children's Adherence to 24-hour Movement Recommendations in a Family-Based Health Setting: "3,2,1 Move on Crossover Study".

Physical inactivity is the fourth most important risk factor for mortality worldwide and it contributes to weight gain and obesity. On the contrary, it is established that regular physical activity is a prevention and managerial factor of these non-communicable diseases. Therefore, the goal of this study is to design and evaluate the effectiveness of a 12-week physical exercise and lifestyle improvement training program carried out in a family environment, through a web platform, and with "online" supervision. This platform will improve the physical conditioning and adherence to PE in a "family environment", and to promote good development of the child through physical activities and exercises that can be done as a family at home and/or outside.

Study Overview

Study Type

Interventional

Enrollment (Actual)

100

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

    • Navarra
      • Pamplona, Navarra, Spain, 31006
        • Navarrabiomed, Universidad Pública de Navarra

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

4 years to 5 years (Child)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Participants without any physical or mental disorders that would prevent them from completing the assessments tests or participating in the exercise intervention program
  • One parent/guardian must answer the questionnaires
  • Informed consent from the participants parent(s)/guardian(s)

Exclusion Criteria:

  • Participants with psychiatric disorders or chronic illness that limits their participation in physical activities
  • Participants who do not comply with the established procedures
  • Participants who do not understand the Spanish language

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: Crossover Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Gamified online exercise in a family environment
Strength training Resistance training Flexibility training Basic motor skills training Executive function training
Participants will complete a 2-days-a-week online training routine with their families: Each session will include a Warm-Up/Activation phase (3 minutes: light intensity continuous training), a Training phase (10-26 minutes: 6-12 repetitions, 20-40" of work, 10-20" recovery), and a Cool Down phase (3 minutes: static and dynamic exercises). The exercises will be different each week and will increase in length and intensity accordingly. The sessions will be supervised by the participants parent(s) and/or guardian(s).
Active Comparator: Standard care Non-supervised daily routines/activities
Non-supervised daily routines/activities
This group will be allocated to standard care and therefore no gamified online exercise training will be provided. They will continue to perform their daily routine/activities including their basic motor skills classes at school and their extracurricular sports and/or cultural activities.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in 24-h movement behaviors (accelerometers) sedentary time.
Time Frame: Baseline, 12 Week, and 24 Week
During their visit to Navarrabiomed, participants will receive a (GENEActiv, Activinsights, Kimbolton, UK) accelerometer that will objectively measure their 24-hour movement behaviors (physical activity, sedentary behaviors, and sleep). The participants will wear the accelerometer for seven consecutive days. Additionally, this accelerometer data will be supplemented with a diary to validate sleep time and (non)wear time.
Baseline, 12 Week, and 24 Week

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in body composition.
Time Frame: Baseline, 12 Week, and 24 Week
Body composition measured with bioelectrical impedance (fat mass and body mass).
Baseline, 12 Week, and 24 Week
Changes in muscle composition.
Time Frame: Baseline, 12 Week, and 24 Week
Muscle composition measured with ultrasound of the thigh/quadriceps/recto femoral.
Baseline, 12 Week, and 24 Week
Changes in health-related physical fitness.
Time Frame: Baseline, 12 Week, and 24 Week
Health-related physical fitness measured, among other tests from the PREFIT battery, with the 20-meter shuttle run test, the handgrip test and the 4x10 speed agility test.
Baseline, 12 Week, and 24 Week
Changes in Basic Motor Skills.
Time Frame: Baseline, 12 Week, and 24 Week
Measured with the MOBAK-KG Battery with tests such as the long jump or balance over an inverted beam. MOBAK-KG sum score ranging from 0 (lowest basic motor competencies) to 16 points (highest basic motor competencies).
Baseline, 12 Week, and 24 Week
Changes in 24-h movement behaviors (self-reported).
Time Frame: Baseline, 12 Week, and 24 Week
Self-report of physical activity levels and sedentary behaviors in youth will assessed by the Youth Activity Profile - Spain. In this questionnaire, a rating scale is used with a score from 1 to 5 in which, in the first two sections, "1" indicates low intensity and frequency of physical activity and "5" indicates high intensity and frequency of physical activity; while, in the third section, "1" indicates a low amount of sedentary behaviors and "5" an excess of them.
Baseline, 12 Week, and 24 Week
Changes in executive function.
Time Frame: Baseline, 12 Week, and 24 Week
Measured with "Early Tools" games (Years Toolbox YET-2017).
Baseline, 12 Week, and 24 Week
Changes in Child Self-Regulation & Behavior.
Time Frame: Baseline, 12 Week, and 24 Week
Measured with CSBQ (Child Self-Regulation & Behavior Questionnaire). Parents will be asked to think about their child's behavior during the past 6 months, and to choose whether each statement was: Not true (1), Somewhat true (2), Certainly true (3), or Can't say (4).
Baseline, 12 Week, and 24 Week
Changes in quality of life.
Time Frame: Baseline, 12 Week, and 24 Week
Kiddy-KINDL will be used to assess the health-related quality of life in children.
Baseline, 12 Week, and 24 Week

Collaborators and Investigators

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

Investigators

  • Study Chair: Alicia Mª Alonso Martínez, Ph.D, Universidad Pública de Navarra

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)

November 1, 2022

Primary Completion (Actual)

May 31, 2023

Study Completion (Actual)

December 31, 2023

Study Registration Dates

First Submitted

February 3, 2023

First Submitted That Met QC Criteria

February 14, 2023

First Posted (Actual)

February 23, 2023

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

February 28, 2025

Last Verified

February 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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