Child Abuse and Neglect Awareness Training in Nursing Students
CANAT
Effect of Child Abuse and Neglect Awareness Training on Nursing Students: A Randomized Controlled Trial
2 other identifiers
interventional
120
1 country
1
Brief Summary
This randomized controlled study aims to evaluate the effect of a child abuse and neglect awareness training program on the knowledge and awareness levels of nursing students. Child abuse and neglect remain significant global public health issues, and healthcare professionals, particularly nurses, play a key role in early recognition and intervention. The study will be conducted among undergraduate nursing students at a university in Istanbul, Turkey. Participants will be randomly assigned to either an experimental group or a control group. Both groups will complete a pre-test to assess baseline knowledge levels. The experimental group will receive a structured training program on child abuse and neglect delivered by an expert nurse working at a Child Advocacy Center under the Ministry of Health, while the control group will not receive any intervention during the study period. One month after the intervention, both groups will complete a post-test to assess changes in knowledge and awareness levels. The primary outcome of the study is the difference in awareness test scores between the pre-test and post-test. The findings are expected to contribute to improving educational strategies and enhancing the competencies of future nurses in recognizing and managing child abuse and neglect cases.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Apr 2026
Shorter than P25 for not_applicable
1 active site
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 Start
First participant enrolled
April 1, 2026
CompletedFirst Submitted
Initial submission to the registry
April 2, 2026
CompletedFirst Posted
Study publicly available on registry
April 13, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 15, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
June 30, 2026
ExpectedApril 15, 2026
April 1, 2026
3 months
April 2, 2026
April 11, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Child Abuse and Neglect Awareness Score
The primary outcome is the change in awareness levels measured using the "Child Abuse and Neglect Awareness Scale (ÇİFÖ)". The scale was developed by Altan (2015) and consists of 20 items, including 11 negatively worded and 9 positively worded items. It is a 5-point Likert-type scale ranging from 1 (strongly disagree) to 5 (strongly agree). Total scores range from 20 to 100, with higher scores indicating greater awareness of child abuse and neglect. The scale will be administered before the intervention (pre-test) and one month after the intervention (post-test).
Baseline and 1 month after the intervention
Secondary Outcomes (1)
Between-Group Difference in Awareness Scores
1 month after intervention
Study Arms (2)
Experimental Group
EXPERIMENTALParticipants receive a structured child abuse and neglect awareness training delivered by an expert nurse.
Control Group
OTHERParticipants do not receive any training during the study period.
Interventions
A structured educational program delivered by an expert nurse working at a Child Advocacy Center, covering types, signs, legal aspects, and management of child abuse and neglect.
Participants in the control group will not receive any training or intervention during the study period. After completion of data collection, the training will be offered to the control group for ethical considerations.
Eligibility Criteria
You may qualify if:
- Being an undergraduate nursing student
- Being able to read and understand Turkish
- Willingness to participate in the study
- Providing written informed consent
You may not qualify if:
- Not completing the training program
- Not completing the pre-test or post-test
- Withdrawing from the study at any stage
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Istanbul Arel University
Istanbul, Turkey (Türkiye)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Masking Details
- This study is open-label as participants and investigators are aware of group assignments. No blinding is applied due to the nature of the educational intervention.
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor, Department of Nursing
Study Record Dates
First Submitted
April 2, 2026
First Posted
April 13, 2026
Study Start
April 1, 2026
Primary Completion
June 15, 2026
Study Completion (Estimated)
June 30, 2026
Last Updated
April 15, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share