Audiovisual Education Impact on Breast Cancer Screening Fear in Illiterate Women
Education
Breast Diseases+3
+ Breast Neoplasms
+ Neoplasms
Supportive Care Study
Summary
Study start date: September 15, 2024
Actual date on which the first participant was enrolled.This study aims to explore the impact of using audio-visual education and simulation techniques on breast cancer screening behaviors and reducing fear of breast cancer among illiterate women. The research is conducted in villages located more than 100 kilometers away from any healthcare facilities in the south of Turkey. It specifically targets women who cannot read or write, addressing a critical need for effective communication and education methods to enhance their understanding and engagement in breast cancer screening. By focusing on this population, the study seeks to potentially improve screening rates and reduce anxiety related to breast cancer, addressing a significant gap in healthcare access for these women. In this study, 120 women participated, divided equally into two groups: an intervention group and a control group. The intervention group received education through audio-visual methods and simulation techniques, while the control group did not receive this specific type of education. The study uses a randomized controlled trial method, ensuring that participants are randomly assigned to each group to accurately measure the effectiveness of the intervention. By comparing the outcomes between the two groups, researchers aim to determine if the audio-visual education method can decrease fear and increase participation in breast cancer screening. This approach not only looks at educational impact but also strives to create a model for improving health education in populations with limited literacy.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.160 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Supportive Care Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Female
Biological sex of participants that are eligible to enroll.From 40 to 69 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
Active ComparatorStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Burdur Mehmet Akif Ersoy University
Burdur, Turkey (Türkiye)Open Burdur Mehmet Akif Ersoy University in Google Maps