- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05741879
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
Status
Completed
Intervention / Treatment
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.
Sponsor
Collaborators
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- PI_2021/111
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.
Clinical Trials on Obesity, Childhood
-
Universiteit LeidenWageningen University; Nutricia, Inc.; Danone ResearchCompletedChildhood Obesity | Childhood Overweight | Vegetable Acceptance in Early ChildhoodNetherlands
-
Cornell UniversityCompletedChildhood Obesity Prevention
-
Universidad de SonoraCentro de Investigación en Alimentación y Desarrollo A.C.; Instituto Nacional...Not yet recruitingChildhood Obesity Pevention
-
Tehran University of Medical SciencesUnknownChildhood Obesity PreventionIran, Islamic Republic of
-
Universidad Autonoma de Nuevo LeonUniversidad de la SabanaCompletedPrevention Childhood ObesityMexico
-
Oregon State UniversityCompletedChildhood Obesity Prevention
-
The Miriam HospitalHassenfeld Child Health Innovation InstituteCompletedChildhood Obesity PreventionUnited States
-
Fundacion para la Formacion e Investigacion Sanitarias...UnknownChildhood Obesity PreventionSpain
-
Tampere UniversitySeinajoki Central Hospital; Tampere University Hospital; Foundation for Paediatric... and other collaboratorsCompleted
-
Harokopio UniversityCompletedPrevention of Childhood ObesityGreece
Clinical Trials on Gamified exercise training
-
Northeast Normal UniversityEnrolling by invitationSensory Integration DysfunctionChina
-
Lokman Hekim UniversityCompletedHealth Education | Adolescent Health | Gamification | Menstrual Hygiene | Genital Hygiene BehaviorsTurkey (Türkiye)
-
University of Texas at AustinCompleted
-
Northeast Normal UniversityCompleted
-
Northeastern UniversityOregon Health and Science University; University of California, RiversideRecruiting
-
Pernille Louise KjeldsenUniversity of Aarhus; Innovation Fund Denmark; Brain+ ApS; Eurostars EUREKANot yet recruitingMild Cognitive ImpairmentDenmark
-
Universitat de LleidaUniversity of Maryland, Baltimore; University of TurkuRecruiting
-
Ondokuz Mayıs UniversityCompletedNursing Education | Patient Safety | Medication SafetyTurkey (Türkiye)
-
Mehmet Akif Ersoy UniversityMassachusetts College of Pharmacy and Health Science; University of Massachusetts...Not yet recruitingPressure Ulcer Prevention | Pressure InjuriesUnited States
-
Chinese University of Hong KongRecruitingAnxiety | Resilience | Depressive SymptomHong Kong