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Development and Feasibility of an Intervention to Increase Physical Activity Among Young Children

Primary Purpose

Childhood Obesity, Physical Activity

Status
Not yet recruiting
Phase
Not Applicable
Locations
Saudi Arabia
Study Type
Interventional
Intervention
I'm an Active Hero (IAAH) Intervention Program
Sponsored by
Queen's University, Belfast
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Childhood Obesity focused on measuring Feasibility, Physical activity, Young Children, Intervention,

Eligibility Criteria

3 Years - 5 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Children in the preschool years, ages 3 to 5, whose parents or guardians consent to their participation in the study An ambulatory individual who does not require physical assistance Children who able to follow verbal instructions Exclusion Criteria: Children older than 5 years old Children for whom parental/caregiver consent is not provided Children with a concurrent medical condition that affects their ability to physically walk a certain distance or with health issues that might influence their participation in the intervention

Sites / Locations

  • General Administration of Education in Taif-KSA

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

I'm an Active Hero (IAAH) Intervention program (intervention group)

Usual physical activities (control group)

Arm Description

Preschool where the intervention implement will be run.

No intervention will be delivered in the control group, and children were requested to continue their usual physical activities.

Outcomes

Primary Outcome Measures

Preschool Facilities that Agreed to Participate
The proportion of preschools that agreed to take part in the study.(Outcome related to trial feasibility)
Preschool Retention
The percentage of preschools which were retained throughout the study.(Outcome related to trial feasibility)
Participant Recruitment
The expected number of participants to be recruited in this study. (Outcome related to trial feasibility).
Participants Retention
The proportion of participants who will complete outcome assessments In either (intervention and control group).(Outcome related to trial feasibility).
Baseline Week ActiGraph Accelerometers-GT3X Return Rate at the End of the Baseline Week
Number of children who will return their ActiGraph accelerometers-GT3X at the end of baseline week on the scheduled day (all children wore the accelerometers simultaneously)
Return of ActiGraph Accelerometers-GT3X on Time by Post-baseline Week Participants
The number of participants who will return their ActiGraph accelerometers-GT3X to the researcher on the designated day, at end of post-baseline week.
Damaged or Lost ActiGraph Accelerometers-GT3X
Number of ActiGraph accelerometers-GT3X that may loss or damage during this study
Intervention Fidelity
Intervention fidelity will be undertaken using the teacher's logbook of the number of sessions conducted per week and structure followed in relation to classroom guides) and observing the delivery of interventions, including two sessions of physical activity and sedentary behaviour will be observed at intervention pre-school at the midpoint through the intervention. At the end of the intervention, teachers and parents will be asked to take part in focus group and /or questionnaires.(Outcome related to trial feasibility).
Acceptability : Intervention Acceptance
Intervention acceptance will be assessed via a post-intervention acceptance questionnaire and/or qualitative data from a post-intervention focus group.(outcome related to trial acceptability).

Secondary Outcome Measures

Change in Body Mass Index (BMI z-score) Measurement
Height (to 0.1cm) and weight (to 0.1kg) will be measured twice without socks or shoes, in indoor clothing. BMI will then derive, and z -scores created relative to UK1990 data.
Change in Participants Physical Activity from Baseline to Post-intervention
The children's preschool and home physical activity will be monitored objectively using the ActiGraph accelerometers-GT3X to be worn for four consecutive days at baseline and again for four consecutive days in week 11 of the trial. The unit of measurement will be the daily mean of time spent in light, and moderate-vigorous physical activity (LMVPA).
Change in Participants Sedentary Behaviour from Baseline to Post-intervention
The children's preschool and home sedentary behaviour will be measured objectively using the ActiGraph accelerometers-GT3X to be worn at baseline for Four consecutive days and in week 11 of the study again for four consecutive days

Full Information

First Posted
February 6, 2023
Last Updated
March 1, 2023
Sponsor
Queen's University, Belfast
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1. Study Identification

Unique Protocol Identification Number
NCT05754359
Brief Title
Development and Feasibility of an Intervention to Increase Physical Activity Among Young Children
Official Title
Feasibility of an Intervention to Promote Physical Activity in Preschool Children: A Cluster Randomised Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
March 2023 (Anticipated)
Primary Completion Date
September 2023 (Anticipated)
Study Completion Date
September 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Queen's University, Belfast

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of this study is to develop, implement, and evaluate a novel intervention to increase physical activity and reduce sedentary behaviour among pre-school children, with the ultimate goal of reducing obesity among this age group. This study will provide evidence-based recommendations for reducing the prevalence of obesity among preschool-aged children, and the suggestions will help improve the physical activity intervention programme in preschoolers.
Detailed Description
The pre-school-based I'm an Active Hero (IAAH) intervention with family involvement was developed in accordance with the Medical Research Council (MRC) framework for developing and evaluating complex interventions. The development phase consists of locating and synthesising existing evidence (such as what is already known about existing interventions) and finding and developing theories (e.g., developing a theoretical understanding of the expected process of behaviour change). The IAAH-intervention components are theory- and evidence-based; they were developed based on a comprehensive identification and evaluation of current and past community, preschool, and family-based physical activity and lifestyle change interventions, as well as recommendations from a recent systematic review and review of reviews. Additionally, the IAAH-intervention component was informed by conducting a systematic review to identify promising intervention components, including behaviour change techniques, that are associated with interventions that were able to increase PA in the preschool age group. In addition to conducting a qualitative study with teachers and patients/guardians, investigators will also consult them on the intervention's content and duration. Investigators would consider the suggestions and ideas from the preschool practitioners' and parent/guardian focus group meetings, which will establish the meaning of PA for the two distinct stakeholder groups, their influences on this, and considerations for a future intervention. The Template for Intervention Description and Replication (TIDieR) framework was also used to set up the intervention component. The design of the intervention will employ systematic review and qualitative phases to inform the quantitative, feasibility phase, followed by a further qualitative phase (stakeholders will be involved in the further refinement of the intervention to add richness and depth). Findings from the systematic review and qualitative work will inform the development of the IAAH intervention. Intervention: This will be a feasibility study of a two-arm cluster-randomised controlled trial (RCT) and will consist of an intervention group and a control group with two data collection time points (i.e., baseline and post-intervention) to test the feasibility and efficacy of a 10-week "I'm an Active Hero (IAAH)" programme intervention with the aim of improving physical activity and decreasing sedentary behaviour of preschool children aged between 3 and 5 years in Taif City, Saudi Arabia. Process evaluation: This will be a qualitative study including interviews and/or questionnaires with stakeholders (pre-school principals, teachers, classroom assistants, and parents/guardians) to determine the acceptability of the intervention from the participants' perspectives.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Childhood Obesity, Physical Activity
Keywords
Feasibility, Physical activity, Young Children, Intervention,

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
I'm an Active Hero (IAAH) Intervention program (intervention group)
Arm Type
Experimental
Arm Description
Preschool where the intervention implement will be run.
Arm Title
Usual physical activities (control group)
Arm Type
No Intervention
Arm Description
No intervention will be delivered in the control group, and children were requested to continue their usual physical activities.
Intervention Type
Behavioral
Intervention Name(s)
I'm an Active Hero (IAAH) Intervention Program
Intervention Description
The "I'm an Active Hero (IAAH)" programme is a 10-week intervention aimed at increasing physical activity and decreasing sedentary behaviour in preschool-aged (aged 3-5 years) children. It is anticipated to begin in February 2023 to May 2023. Assessments will be conducted at baseline and immediately following the intervention. The IAAH-intervention will be implemented by the preschool teachers, who will have two teacher training sessions with the main researcher (myself). The IAAH-intervention involves environmental modifications (a classroom) to create areas with sufficient space for active play; classroom sessions these will be implemented for 10 weeks (a minimum of one hour per week); and parent involvement, such as the provision of parental-child interaction homework activities and written information (tip cards, posters, and newsletters). for parents on how to encourage their children to be active.
Primary Outcome Measure Information:
Title
Preschool Facilities that Agreed to Participate
Description
The proportion of preschools that agreed to take part in the study.(Outcome related to trial feasibility)
Time Frame
10 weeks
Title
Preschool Retention
Description
The percentage of preschools which were retained throughout the study.(Outcome related to trial feasibility)
Time Frame
10 weeks post baseline
Title
Participant Recruitment
Description
The expected number of participants to be recruited in this study. (Outcome related to trial feasibility).
Time Frame
10 weeks
Title
Participants Retention
Description
The proportion of participants who will complete outcome assessments In either (intervention and control group).(Outcome related to trial feasibility).
Time Frame
10 weeks post baseline
Title
Baseline Week ActiGraph Accelerometers-GT3X Return Rate at the End of the Baseline Week
Description
Number of children who will return their ActiGraph accelerometers-GT3X at the end of baseline week on the scheduled day (all children wore the accelerometers simultaneously)
Time Frame
1 week
Title
Return of ActiGraph Accelerometers-GT3X on Time by Post-baseline Week Participants
Description
The number of participants who will return their ActiGraph accelerometers-GT3X to the researcher on the designated day, at end of post-baseline week.
Time Frame
10 weeks after baseline
Title
Damaged or Lost ActiGraph Accelerometers-GT3X
Description
Number of ActiGraph accelerometers-GT3X that may loss or damage during this study
Time Frame
11 weeks (1 week at baseline and 10 weeks after baseline
Title
Intervention Fidelity
Description
Intervention fidelity will be undertaken using the teacher's logbook of the number of sessions conducted per week and structure followed in relation to classroom guides) and observing the delivery of interventions, including two sessions of physical activity and sedentary behaviour will be observed at intervention pre-school at the midpoint through the intervention. At the end of the intervention, teachers and parents will be asked to take part in focus group and /or questionnaires.(Outcome related to trial feasibility).
Time Frame
10 weeks
Title
Acceptability : Intervention Acceptance
Description
Intervention acceptance will be assessed via a post-intervention acceptance questionnaire and/or qualitative data from a post-intervention focus group.(outcome related to trial acceptability).
Time Frame
1 week after the end of the intervention
Secondary Outcome Measure Information:
Title
Change in Body Mass Index (BMI z-score) Measurement
Description
Height (to 0.1cm) and weight (to 0.1kg) will be measured twice without socks or shoes, in indoor clothing. BMI will then derive, and z -scores created relative to UK1990 data.
Time Frame
Baseline and 10 weeks post-intervention
Title
Change in Participants Physical Activity from Baseline to Post-intervention
Description
The children's preschool and home physical activity will be monitored objectively using the ActiGraph accelerometers-GT3X to be worn for four consecutive days at baseline and again for four consecutive days in week 11 of the trial. The unit of measurement will be the daily mean of time spent in light, and moderate-vigorous physical activity (LMVPA).
Time Frame
Baseline and 10 weeks post-intervention
Title
Change in Participants Sedentary Behaviour from Baseline to Post-intervention
Description
The children's preschool and home sedentary behaviour will be measured objectively using the ActiGraph accelerometers-GT3X to be worn at baseline for Four consecutive days and in week 11 of the study again for four consecutive days
Time Frame
Baseline and 10 weeks post-intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
5 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Children in the preschool years, ages 3 to 5, whose parents or guardians consent to their participation in the study An ambulatory individual who does not require physical assistance Children who able to follow verbal instructions Exclusion Criteria: Children older than 5 years old Children for whom parental/caregiver consent is not provided Children with a concurrent medical condition that affects their ability to physically walk a certain distance or with health issues that might influence their participation in the intervention
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Neil Heron, PhD
Phone
+44 (0)28 9097 6056
Email
N.Heron@qub.ac.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Neil Heron, PhD
Organizational Affiliation
Queen's University, Belfast
Official's Role
Principal Investigator
Facility Information:
Facility Name
General Administration of Education in Taif-KSA
City
Taif
State/Province
Maccha
ZIP/Postal Code
26523
Country
Saudi Arabia
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mosfer ALwalah
Phone
009667272020
Ext
2112
Email
malwalah01@qub.ac.sa

12. IPD Sharing Statement

Plan to Share IPD
No

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Development and Feasibility of an Intervention to Increase Physical Activity Among Young Children

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