Simple Simulation Based Breast Cancer Awareness Training

NCT ID: NCT06528808

Last Updated: 2024-07-30

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

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-09-01

Study Completion Date

2024-10-30

Brief Summary

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It was planned to determine the effect of simple simulation-based breast cancer awareness training on women's breast cancer knowledge and fear levels. The research population will consist of female service personnel working in institutions within the University of Health Sciences (SBÜ) (N: 670). In order to determine the sample size in this research, which was planned as a quasi-experimental with a pre- and post-test design and a control group; The data showed a normal distribution, the standard deviation of the population was estimated to be 1, and the effect size (difference) was estimated to be 0.8. It was calculated that if two independent n₁=40, n₂=40 samples were taken for the analysis to be carried out, at a 5% significance level, the maximum power value of the research would be 0.942182. Both groups will be given theoretical training about breast cancer awareness, and women in the intervention group will practice breast cancer awareness with a simple valid simulator. All groups will be informed before the applications. The training content will be supported by distributing a 5-page training booklet created from breast health and cancer awareness content to the participants. "Comprehensive Breast Cancer Knowledge Test", "Breast Cancer Fear Scale" and "Breast Cancer Awareness Scale" will be applied as a pre-test after the information.

Detailed Description

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Conditions

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Breast Cancer Awareness Training

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Quasi-experimental randomized controlled trial
Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Participants

Study Groups

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İntervention group (n:40)

Women in the intervention group will undergo a simulator breast cancer awareness application in simple reality.

Group Type EXPERIMENTAL

Simple reality simulator application

Intervention Type OTHER

Women in the intervention group will be given an application aimed at breast cancer awareness with a simple valid simulator.

Control group (n:40)

Control group women will receive 2 hours of theoretical training.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Simple reality simulator application

Women in the intervention group will be given an application aimed at breast cancer awareness with a simple valid simulator.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Volunteering to participate in the research.
* To work as female service personnel in institutions within the University of Health Sciences.

Exclusion Criteria

\- Not participating in all applications of simulation teaching.
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Saglik Bilimleri Universitesi

OTHER

Sponsor Role lead

Responsible Party

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YASEMİN AYDIN KARTAL

Assoc. Prof. Dr.

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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University of Health Sciences

Istanbul, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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SBÜ-AYDINKARTAL-007

Identifier Type: -

Identifier Source: org_study_id

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