Effectiveness of The Diagnostic Training on The Signs and Rısks of Child Abuse and Neglect Given By The Tell-What You Have Learned Method

NCT ID: NCT07106099

Last Updated: 2025-08-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

86 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-01-01

Study Completion Date

2024-06-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The research, planned in an experimental design with a pretest-posttest control group, was conducted with second-year students studying at the Department of Midwifery (n=86). The students participating in the study were divided into intervention (n: 43) and control (n: 43) groups by simple random sampling. Training in identifying the symptoms and risks of child abuse and neglect was given to the intervention group students with the explain method, while the control group was given classical training. In collecting data; 'Introductory Information Form', 'Identification Scale for Symptoms and Risks of Child Abuse and Neglect', and 'Child Abuse and Neglect Awareness Scale' were used. Data were collected before the application and at the 4th week after the application.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The implementation phase of the research was carried out in the classroom of the Midwifery Department at the Faculty of Health Sciences of a public university. During the training sessions, all student activities were observed by the researchers.

Second-year midwifery students (n=86) were randomly assigned by the researchers to the intervention group (n=43) and the control group (n=43) using the website https://www.randomizer.org/. An introductory information form was administered to all participants, and a briefing session was held before the implementation. In this session, detailed information about the procedures to be carried out in the study was provided, and a question-and-answer session was conducted. Students were informed about the training plan's flowchart, content, process, and environment. It was explained that the intervention group (n=43) would be trained on identifying signs and risks of child abuse and neglect using the "teach-back method," while the control group (n=43) would receive traditional education on the same topic.

Before the training, as a pretest, the "Scale for Identifying Signs and Risks of Child Abuse and Neglect" and the "Child Abuse and Neglect Awareness Scale" were administered to all participants. All groups were given a 2-hour theoretical session on child abuse and neglect via a PowerPoint presentation. During the session, students' questions were addressed. At the end of the training, all students were asked to leave the classroom. Subsequently, intervention group students were brought back individually and asked to explain the training content in their own words. After their explanations, they were asked additional questions such as "Is there anything you would like to add?" and "Can you provide examples related to the topic?" to encourage further elaboration.

Four weeks after the training, all participants were administered the same scales as a posttest: the "Scale for Identifying Signs and Risks of Child Abuse and Neglect" and the "Child Abuse and Neglect Awareness Scale."

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Child Abuse Neglect

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

SINGLE

Investigators

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

control group (n:43)

Students in the control group will be given 2 hours of training on diagnosing the symptoms and risks of child abuse and neglect using the classical method.

Group Type NO_INTERVENTION

No interventions assigned to this group

intervention group (n:43)

Students in the intervention group will be given training on identifying the symptoms and risks of child abuse and neglect using the tell-what-you-learned method.

Group Type EXPERIMENTAL

Training given with the tell-what-you-learned method

Intervention Type BEHAVIORAL

Students in the intervention group will be given training on diagnosing the symptoms and risks of child abuse and neglect, given by the tell-what-you-learned method, and will be given a practice in which its effectiveness will be evaluated.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Training given with the tell-what-you-learned method

Students in the intervention group will be given training on diagnosing the symptoms and risks of child abuse and neglect, given by the tell-what-you-learned method, and will be given a practice in which its effectiveness will be evaluated.

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Being a second-year student at the University of Health Sciences, Hamidiye Faculty of Health Sciences, Department of Midwifery
* Volunteering to participate in research

Exclusion Criteria

* Students who do not meet the sample selection criteria
* Not being willing to participate in the study
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Saglik Bilimleri Universitesi

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

YASEMİN AYDIN KARTAL

Associate Professor Dr.

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Yasemin AYDIN KARTAL, Doç. Dr.

Role: PRINCIPAL_INVESTIGATOR

[email protected]

Büşra HIZLIOL, Arş. Gör.

Role: STUDY_CHAIR

[email protected]

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Sağlık Bilimleri Üniversitesi

Istanbul, , Turkey (Türkiye)

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

SBÜ-AYDINKARTAL-009

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.