- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06410573
The Effect Of Self-Breast Examination Training On The Belief Of Breast Health
May 10, 2024 updated by: KTO Karatay University
The Effect Of Self-Breast Examination Training Provided To Women Between 18 And 49 Years Of Age And Practice On The Belief Of Breast Health: A Randomized Controlled Study
The aim of the present research was to detect the effect of self-breast examination provided to women between 18 and 49 years of age and practice on the belief of women on their breast health.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The aim of this study was to investigate the effect of breast self-examination training and practice on breast health beliefs.
The study was a pretest-posttest randomized controlled experimental design.
Women in the experimental group of the study will be provided with the training prepared by the researcher.
The presentation used in the training will include information about breast cancer, breast cancer screening programs and breast self-examination.
In the presentation, the steps of breast self-examination were shown step by step using visual materials.
In addition to the slide presentation about breast cancer and breast self-examination, women will be trained on breast self-examination with a breast examination model using the "show first, then do it" training technique, and the accuracy will be confirmed by asking women to do it.
By using the model in breast examination, it will be determined what women do right and what they do wrong during the examination.
Data will be collected with Personal Information Form and Champion Health Belief Model Scale.
Study Type
Interventional
Enrollment (Actual)
98
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
-
-
Karatay
-
Konya, Karatay, Turkey
- KTO Karatay University
-
-
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
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Fertility process to continue
- No communication problems
- Not having a disease that will affect perception
Exclusion Criteria:
- Having been previously diagnosed with breast cancer or receiving breast cancer treatment
- Being diagnosed with a medical mental illness and receiving treatment for this reason
- Being under active treatment in hospital due to any problem
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: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Training on Breast Self-Examination
In the training, women will be divided into 5 groups and the training will be held in 5 separate sessions in one day.
A training program will be completed with 9 women.
All trainings will be conducted under the same conditions in the school's training room.
Before the training, women will be informed about the training and their permission and consent will be obtained.
The training prepared by the researcher will be presented to the women in the experimental group of the study.
The presentation used in the training will include information about breast cancer, breast cancer screening programs and breast self-examination.
|
In the training, women will be divided into 5 groups and the training will be held in 5 separate sessions in one day.
A training program will be completed with 9 women.
All trainings will be conducted under the same conditions in the school's training room.
Before the training, women will be informed about the training and their permission and consent will be obtained.
The training prepared by the researcher will be presented to the women in the experimental group of the study.
The presentation used in the training will include information about breast cancer, breast cancer screening programs and breast self-examination.
In the presentation, the steps of breast self-examination will be shown step by step using visual materials.
|
|
No Intervention: Control
1 week follow-up.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Breast Self-Examination Training and Breast Health Beliefs
Time Frame: 1 month will be followed
|
This outcome is assessed with the Champion Health Belief Model Scale.
A higher score on the scale indicates an increase in sensitivity and caring, a higher perception of benefits for the perception of benefits, and a higher perception of obstacles for the perception of obstacles.
|
1 month will be followed
|
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)
November 6, 2022
Primary Completion (Actual)
February 1, 2023
Study Completion (Actual)
March 1, 2023
Study Registration Dates
First Submitted
June 1, 2023
First Submitted That Met QC Criteria
May 10, 2024
First Posted (Actual)
May 13, 2024
Study Record Updates
Last Update Posted (Actual)
May 13, 2024
Last Update Submitted That Met QC Criteria
May 10, 2024
Last Verified
May 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- KaratayUH9
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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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