NCT06981416

Brief Summary

Childhood home accidents are a significant health problem in our country and the world. Home accidents are more common in children aged 1-5, and cause temporary and permanent disabilities in deaths. In the project proposal, it is planned to conduct a randomized controlled trial to determine the effects of digital and classical home accident and first aid training given to mothers in the risk group with children aged 1-3 in line with the Planned Behavior Theory (PDT) on home accident safety precautions and first aid self-efficacy. In the study, the features of the education model that will provide original value and original contribution are that it is digitally based (animated video) education, which will allow individuals to receive training at their own pace and in accordance with their needs due to its individualizable feature. This will encourage mothers to participate more at the appropriate time and actively participate in the training. It is a more cost-effective and time-saving application compared to other teaching materials. In addition, it is original in that the group to be trained is mothers in the risk group. It is different from other studies on 'home accidents' in that it is planned in line with the PDT, randomized controlled, and the outputs will be measured with repeated measurements. The implementation of this project will consist of four main stages. In the first stage, the creation of the educational content, preparation of digital and classical educational materials in line with expert opinions and their evaluation by expert opinions. In the second stage, the final version will be arranged in line with the preliminary application. In the third stage, the implementation of the initiative and the collection of data. In the fourth stage, the statistical analysis of the data. The total duration of the project will be divided into approximately 3 months in the first stage, 1 month in the second, 7 months in the third and the last stage in the 1-month stage. In order for the project to be carried out healthily and effectively, the project manager and the doctoral student specialist nurse will take part. Since the project is original, if it is successful, there is a high probability that a doctoral thesis will be formed. It is highly likely that a researcher with a doctorate title will be formed upon completion of the project. The importance of the digital education method is very clear and its active use in nursing education will positively contribute to the development of child and family health. It is highly probable that the training model to be created will be recommended for use in secondary and tertiary healthcare institutions, including primary healthcare.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
108

participants targeted

Target at P50-P75 for not_applicable

Timeline
1mo left

Started Jun 2025

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress90%
Jun 2025Jun 2026

First Submitted

Initial submission to the registry

April 21, 2025

Completed
29 days until next milestone

First Posted

Study publicly available on registry

May 20, 2025

Completed
26 days until next milestone

Study Start

First participant enrolled

June 15, 2025

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 15, 2025

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 15, 2026

Expected
Last Updated

May 20, 2025

Status Verified

May 1, 2025

Enrollment Period

6 months

First QC Date

April 21, 2025

Last Update Submit

May 13, 2025

Conditions

Keywords

Drowning, Child, Fall, Electric Shock, Home accidents, First Aid, Burn, Poisoning,

Outcome Measures

Primary Outcomes (2)

  • Scale for Identifying Mothers' Safety Measures Against Home Accidents in 6-Year-Old Children

    The scale was developed by Çınar and Görak (2003). The scale defines the precautions taken by mothers with children between the ages of 0-6 to protect themselves from home accidents. The scale consists of 40 items, 34 of which are positively expressed and 6 of which are negatively expressed. The scale is a five-point Likert-type scale, with 34 questions containing positive expressions being scored as always 5 points, often 4 points, sometimes 3 points, rarely 2 points, and never 1 point. Propositions containing negative expressions are items 6, 9, 23, 26, 30, and 40, and the scoring is done in reverse. The minimum scale score is 40, and the maximum scale score is 200 points. As the score obtained from the scale increases, the level of precautions taken by parents increases. The Croncbach alpha internal consistency coefficient value is 0.82

    before the educational (pre-test), after the educational (post-test) and after the education 3 months (follow-up)

  • Self-Efficacy of First Aid Scale for Home Accidents

    he original scale name is "Self-Efficacy of First Aid Scale For Home Accidents" and was developed by Wei and colleagues in 2013 (Wei et al 2013). The scale was adapted to Turkish by Altundağ, Turan and Şafak (2020). The Self-Efficacy of First Aid Scale for Home Accidents consists of 12 items that include interventions that the mother can implement in the event of home accidents. The scale expressions are five-point Likert-type and are indicated as completely agree (100%), completely disagree (0). Higher scores indicate better self-efficacy in first aid. The Cronbach's alpha value of the scale was found to be 0.89

    before the educational (pre-test), after the educational (post-test) and after the education 3 months (follow-up)

Study Arms (3)

intervention group (Dijital education)

EXPERIMENTAL

The mothers in this group will be given an educational animation video based on the "Planned Behavior Theory" as a single session asl digital training.

Behavioral: Digital education group

intervention group (classical education)

EXPERIMENTAL

The mothers in this group will receive classical education in the form of a flow chart, with educational content prepared according to the "Planned Behavior Theory".

Behavioral: classical education group

Control Group

NO INTERVENTION

No intervention

Interventions

Digital training for home accidents and first aid based on the Theory of Planned Behavior (PBT) and the pre-test, post-test and follow-up results will be evaluated.

Also known as: intervention1
intervention group (Dijital education)

The training content prepared according to the "Planned Behavior Theory" will be given as classical training in the form of a flow chart.

Also known as: intervention2
intervention group (classical education)

Eligibility Criteria

AgeUp to 55 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsMothers will be included in the study.
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Being a mother with a 1-3 year old child,
  • Having a low socioeconomic status (income below the poverty line) https://www.who.int/data/gho/indicator-metadata-registry/imr-details/4744 ,
  • Being the primary caregiver is the mother,
  • The mother is literate,
  • The mother is willing to participate in the study.

You may not qualify if:

  • The child has a mental or physical disability,
  • The mother is a health worker,
  • The mother has been diagnosed with a mental or psychiatric illness

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Selcuk University

Konya, Konya, 42250, Turkey (Türkiye)

Location

MeSH Terms

Conditions

DrowningBurnsPoisoning

Condition Hierarchy (Ancestors)

DeathPathologic ProcessesPathological Conditions, Signs and SymptomsWounds and InjuriesChemically-Induced Disorders

Central Study Contacts

Fatma Tas Arslan, Prof

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

April 21, 2025

First Posted

May 20, 2025

Study Start

June 15, 2025

Primary Completion

December 15, 2025

Study Completion (Estimated)

June 15, 2026

Last Updated

May 20, 2025

Record last verified: 2025-05

Data Sharing

IPD Sharing
Will not share

Locations