- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06248021
Ecological Footprint Awareness Program in 60-72 Months Children
February 7, 2024 updated by: Ayse Sezer Balci, Burdur Mehmet Akif Ersoy University
Effectiveness of Ecological Footprint Awareness Program in 60-72 Months Children: A Randomized Controlled Study
This study aimed to evaluate the effectiveness of an ecological footprint awareness training program for children aged 60-72 months.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This study was conducted using a cluster randomized controlled pretest-posttest experimental design.
It was carried out in four kindergartens located in a city center between April and June 2023.
Two of the kindergartens were assigned to the intervention group while the other two were assigned to the control group.
Data was collected using the Ecological Footprint Awareness Scale for Children (EFAS-C).
The training program was conducted with the children in the intervention group for four weeks, with a 40-minute session each week.
The program covered one topic each week, which included waste management, water and energy use, food consumption, and transportation.
The data was analyzed using descriptive statistics, paired groups t-test, and independent groups t-test, with a 95% confidence interval and p<.05 significance level.
Study Type
Interventional
Enrollment (Actual)
66
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
-
-
-
Burdur, Turkey
- Burdur Mehmet Akif Ersoy University
-
-
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
- Child
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- enrolled in the schools where the study was conducted
- Approved by their family to participate in the study,
- 60-72 months old
Exclusion Criteria:
- participation in less than 2/3 of the intervention protocol
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: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Ecological Footprint Awareness Program Group
The program was conducted for four weeks, one day each week, for 40 minutes.
Each week, a different topic was addressed such as waste evaluation, water and energy usage, food consumption, and transportation.
The program was created in line with expert opinions and literature.
|
The program was conducted for four weeks, one day each week, for 40 minutes.
Each week, a different topic was addressed such as waste evaluation, water and energy usage, food consumption, and transportation.
The program was created in line with expert opinions and literature.
The sessions were based on the principles of the Social Cognitive Learning Theory, developed by Bandura, which includes mutual determinism, symbolization, anticipatory capacity, vicarious learning, self-regulation capacity, and self-judgment capacity.
During each session, various techniques such as animation, drawing, storytelling, memory cards, and games were employed.
To ensure the program's content was appropriate for children's development, the opinions of two experts from the child development department of the university were obtained.
|
No Intervention: Control Group
No intervention was applied to the group
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Ecological Footprint Awareness Scale for 60-72 Month-old Children scores
Time Frame: four weeks
|
ıt contains five themes, including 'Water and energy use,' 'Waste utilization,' 'Food consumption,' and 'Transportation'.
It contains a total of 19 items, which are asked through a game and story structure.
he scale is divided into two sections: a game section and a story section.
In the game section, children are shown pictures and asked how the characters should behave.
In the story section, children are told a story and asked which character is behaving in an environmentally friendly way.
Children who answer correctly receive a score of "1", while those who answer incorrectly receive a score of "0".
The total score is used to measure environmental awareness.
The KR-20 coefficient for internal consistency reliability of the EKAY-O was calculated as 0.66.
|
four weeks
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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)
April 2, 2023
Primary Completion (Actual)
June 19, 2023
Study Completion (Actual)
July 24, 2023
Study Registration Dates
First Submitted
January 24, 2024
First Submitted That Met QC Criteria
February 7, 2024
First Posted (Actual)
February 8, 2024
Study Record Updates
Last Update Posted (Actual)
February 8, 2024
Last Update Submitted That Met QC Criteria
February 7, 2024
Last Verified
February 1, 2024
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- ERSOYU-SBF-ASB-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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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