- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06633549
The Effect of Home Accidents Prevention Training Given to Mothers of Mentally Disabled Children
October 13, 2024 updated by: Zeynep Erkut, Maltepe University
Investigation of the Effect of Home Accidents Prevention Training Given to Mothers of Mentally Disabled Children Aged 0-6: A Randomized Controlled Trial
The aim of this research is to examine the effect of education for home accidents given to mothers with mentally disabled children in the age group of 0-6.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This study was conducted to examine the effects of education on home accidents given to mothers of mentally disabled children aged 0-6.
The sample of the study consisted of 83 mothers of mentally disabled children aged 0-6 registered in four special education centers in Kocaeli province between May 2023 and June 2024 (education group: 40 mothers; control group: 43 mothers).
Research data were collected using the Information Form and the Scale for Diagnosing Mothers' Safety Precautions for Home Accidents in 0-6 Year Old Children.
The mothers in the education and control groups were informed about the study, their written consent was obtained, and they were asked to fill out information forms.
The mothers in the education group were given a single, 45-minute face-to-face education on preventing home accidents.
The Mothers' Safety Measures for Home Accidents in Children aged 0-6 were administered the Scale before and one month after the training.
The mothers in the control group did not receive any training; the Scale for Identifying Mothers' Safety Precautions for Home Accidents in Children Aged 0-6 was administered during the first interview and again one month later.
Study Type
Interventional
Enrollment (Actual)
83
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
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-
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Istanbul, Turkey
- Maltepe University
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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
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Mothers with mentally disabled children aged 0-6
- Mothers who agree to participate in the research
- Mothers who agree to be contacted after 1 month for the post-test
- Mothers who know and speak Turkish at the native level
Exclusion Criteria:
- Mothers with mentally disabled children over the age of 6
- Mothers who do not agree to participate in the study
- Mothers who do not agree to be contacted after 1 month for the post-test
- Mothers with mental disabilities
- Mothers who do not know or speak Turkish at the native level
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: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Educated
Educated Group
|
Mothers in the education group who participated in the study were informed about the research and their written consent was obtained.
Mothers filled out the 'Information Form' then completed the 'Diagnostic Scale of the Mother's Safety Measures for Home Accidents in Children Aged 0-6 Years'.
Mothers were helped when filling out the form and their questions were answered.
The training program was organized so that there would be a maximum of 5 mothers in each group.
The trainings were conducted face-to-face with a PowerPoint presentation and lasted about 40-45 minutes.
Question-answer and discussion methods were used during the training.
After the training, the mothers were asked to fill out the same scale again one month later.
One month after the training, the mothers were interviewed face-to-face and the scale was filled in again and the changes they made at home were recorded.
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Other: Uneducated
Uneducated Group (Control)
|
Mothers in the control group were informed about the research and the 'Informed Consent Form' was signed.
The mothers filled out the 'Information Form' and this process took about 15-20 minutes.
Mothers were helped when filling out the form and their questions were answered.
In addition, mothers were asked to complete the 'Diagnostic Scale of the Mother's Safety Measures for Home Accidents in Children Aged 0-6' by introducing.
A month later, they were informed that they had to fill out this scale again.
A month later, the mothers were interviewed face-to-face and allowed to fill out the scale again.
After the last test, the mothers in the control group were given 'Home Accidents and Prevention Training for Children in the 0-6 Age Group' and the output of the training presentation was distributed.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The Scale for Diagnosing the Safety Measures of the Mother for Household Accidents in Children Aged 0-6
Time Frame: Before the training and one month after the training.
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The scale developed by Çınar and colleagues evaluates the safety precautions taken by mothers of children aged 0-6 to protect their children from home accidents (burns, falls, poisoning, sharp-edged injuries, foreign object aspiration, drowning, electric shocks).
The Scale for Identifying Mothers' Safety Precautions for Home Accidents in Children Aged 0-6 consists of a total of 40 items, with 34 positive and 6 negative statements.
Each item is scored between 1-5 on the five-point Likert-type scale.
While the items containing positive statements always receive 5 points, often 4 points, sometimes 3 points, rarely 2 points, and never 1 point, the items containing negative statements receive 6, 9, 23, 26, 30, and 40 never 5 points, rarely 4 points, sometimes 3 points, often 2 points, and always 1 point.
The minimum score of the scale is 40 and the maximum score is 200.
The Croncbach alpha internal consistency coefficient value is 0.82.
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Before the training and one month after the training.
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
May 1, 2023
Primary Completion (Actual)
June 1, 2024
Study Completion (Actual)
June 1, 2024
Study Registration Dates
First Submitted
October 7, 2024
First Submitted That Met QC Criteria
October 7, 2024
First Posted (Actual)
October 9, 2024
Study Record Updates
Last Update Posted (Actual)
October 16, 2024
Last Update Submitted That Met QC Criteria
October 13, 2024
Last Verified
October 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- 2022/21-07
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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