The Effect of Screen to Move Program in Preschool Children

Sponsor
Marmara University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05805592
Collaborator
(none)
100
2
15.3

Study Details

Study Description

Brief Summary

The aim of this study is to determine the effect of the developed program on screen usage time and physical activity for pre-school children.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Screen-to-Move-Program (STEP)
N/A

Detailed Description

The "Screen-to-Move-Program" (STEP), developed on the basis of Social Cognitive Theory (SCT), is aimed to reduce screen usage time and increase physical activity in pre-school children. In this study, it was aimed to increase children's physical activity and decrease screen usage times with a 6 session intervention program based on SCT, which includes children and parents. The effectiveness of the program will be evaluated with the pre-test, post-test and 3rd month follow-up test.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
This study is a parallel group randomized controlled study.This study is a parallel group randomized controlled study.
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
The Effect of Screen to Move Program (STEP) on Screen Use Time and Physical Activity in Preschool Children
Anticipated Study Start Date :
Apr 20, 2023
Anticipated Primary Completion Date :
Sep 25, 2023
Anticipated Study Completion Date :
Jul 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention Group

It is planned as 6 sessions, 1 session per week for children and parents. The program will be introduced to children and parents under the call with "Screen-to-Move-Program (STEP)". The symbol of the program has been created and this symbol will be hung on the classroom door. Sessions for children include story, picture, video demonstration and active playing activities. A more clear, simple and understandable language will be used for children, and reinforcements will be used. For parents; There will be 6 training sessions in the form of presentations. At the same time as the children's activities, information notes will be sent to the parents outlining the expectations. Before the intervention, after the intervention and in the 3rd month, children's screen use time, daily physical activity time, sleep time, parents' knowledge, behavior, attitude and self-efficacy about their children's screen use time will be evaluated.

Behavioral: Screen-to-Move-Program (STEP)
It is planned as 6 sessions, 1 session per week for children and parents. The program will be introduced to children and parents under the call with "Screen-to-Move-Program (STEP)".

No Intervention: Control Group

Screen use time, daily physical activity time, sleep time, parents' knowledge, behavior, attitude and self-efficacy about children's screen use time will be evaluated simultaneously from the control group with the intervention group. After the 3rd month follow-up test, the STEP will be applied to the children and parents in the control group.

Outcome Measures

Primary Outcome Measures

  1. Decreasing screen time of children in the experimental group [Change in screen usage time within 3 months]

    Children's screen usage time will be evaluated with questions. "How long (…hours…..minutes) on average did your child use any device with an electronic screen, such as a smartphone, tablet, video game, or watch television, movies, video games in a day?". Daily screen usage time will be evaluated in minutes. A maximum of 60 minutes of screen time is recommended for pre-school children (World Health Organization, 2019).

  2. Increasing physical activity level of children in the experimental group [Change in physical activity level within 3 months]

    Children's physical activity levels; Item 1: "How long is your child active on average in a day? (e.g. walking slowly, making the bed etc.)" and Item 2:"How long does your child do physical activity in a day, on average, until he is out of breath?" (walking fast, cycling, running, playing ball games, swimming, dancing, etc.) will be evaluated based on parent self-report. The total daily (Item1 + Item2) physical activity time will be evaluated in minutes. A minimum of 180 minutes of physical activity is recommended for pre-school children (World Health Organization, 2019).

  3. Increasing number of steps for the children in the experimental group [Change in number of steps within 3 months]

    Pre-school children's daily step count will be measured with the OMRON HJ-109-E pedometer. In our study, the number of steps for children aged 3-5 will be evaluated as 11,500 steps, which is stated to correspond to the 180 minutes physical activity target recommended by the World Health Organization for children aged 3-5 (De Craemer et al., 2015; World Health Organization, 2019).

Secondary Outcome Measures

  1. Increasing knowledge score of parents in the experimental group [Change in knowledge score of parents within 3 months]

    The information form was created by researchers in line with the literature (World Health Organization, 2019). The form contains information about the PA, screen usage time and sleep duration of the children of parents who have children between the ages of 2-5 and consists of 14 questions. For each item, the correct option is scored as 1, and the incorrect and I don't know option is scored as 0. The total score obtained by collecting the items varies between 0-14 points. A high score indicates a high level of knowledge.

  2. Increase in the attitude score of the parents in the experimental group [Change in parents' attitudes within 3 months]

    Parents' attitudes towards their children's screen time were evaluated with an eight-item questionnaire developed by Zimmerman et al. in 2007. The questionnaire is in a five-point Likert type, ranging from strongly agree (1) to strongly disagree (5). High scores on the survey reflect more positive attitudes. The questionnaire has been used in many studies before and has a high reliability with the cronbach alpha value of .84 (Carson & Janssen, 2012; Mansor et al., 2021; Raj et al., 2022).

  3. Increasing self-efficacy score of parents in the experimental group [Change in self-efficacy score of parents within 3 months]

    Self-efficacy will be measured separately to reduce screen time and increase physical activity. Parents' self-efficacy in reducing their children's screen time: "How confident are you that you can say no to your child's request to participate in screen time (TV/computer/tablet/video games)?" It will be assessed on a 5-point scale ranging from 'not at all sure' to 'very sure' (Carson & Janssen, 2012). The parent's self-efficacy in influencing the child's physical activity reflects the parent's level of confidence in situations related to the child's physical activity. The questionnaire developed in 2010 has a single factor structure and high reliability (α= 0.88). The eight-question survey (For example: How confident are you that your child will do physical activity even if you do not have much time) is a five-point Likert type ranging from I do not trust myself (1) to I am very confident (5). High scores on the questionnaire reflect higher self-efficacy (Smith et al., 2010).

Eligibility Criteria

Criteria

Ages Eligible for Study:
36 Months to 60 Months
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. Children aged 36-60 months and their parents.

  2. Children without any physical and mantel disability

Exclusion Criteria:

1.The data of parents who fill in the data collection forms incompletely will be excluded from the analysis

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Marmara University

Investigators

  • Study Chair: Ayse Ergun, Prof, Marmara University
  • Principal Investigator: Tuba Bay Kula, MSc, RN, Marmara University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Tuba Bay Kula, Principal Investigator, Marmara University
ClinicalTrials.gov Identifier:
NCT05805592
Other Study ID Numbers:
  • 19092293
First Posted:
Apr 10, 2023
Last Update Posted:
Apr 10, 2023
Last Verified:
Mar 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Tuba Bay Kula, Principal Investigator, Marmara University

Study Results

No Results Posted as of Apr 10, 2023