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Clinical Trials in Turkey / NCT06898229
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Effect of Audiovisual Education on Breast Cancer

NCT06898229 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2024-09-15
Last updated
2025-03-27

Condition(s) studied

Breast Cancer

Investigational drug(s) / intervention(s)

Education

Education: The intervention program aimed to increase participation in breast cancer screenings and reduce fear among illiterate women. The three-month training was structured in three phases. In the first month, awareness was raised through visual-audio materials about breast cancer, risk factors, and the importance of early diagnosis. In the second month, practical training was provided on breast self-examination (BSE), and clinical breast examination (CBE) and mammography procedures were introduced. In the final month, group discussions and success stories supported behavioral change, reinforcing knowledge. The program's effectiveness was evaluated through pre-test and post-test comparisons.

Study summary

This study was conducted as a double-blind randomised controlled trial to determine the effect of education using audio-visual methods and simulation techniques on breast cancer screening and breast cancer fears in illiterate women. The study was conducted in the villages of a district in the south of Turkey with a distance of over 100 km to health institutions. The sample size of the study was calculated with the G\*Power 3.1 programme based on the mean breast cancer fear scores (22.42±8.30 for those without family history and 28.14±6.23 for those with family history) in a study, with a 95% confidence interval, 5% margin of error, 0.92 effect size and 95% power. As a result of this analysis, the minimum sample size required was determined as 64 people in total. However, a total of 120 women were included in the study in order to increase the power of the research, to prevent possible data loss and to make the results more reliable. Participants were divided into intervention (n=60) and control (n=60) groups by simple random sampling method.

Eligibility

Sex
FEMALE
Min age
40 Years
Max age
69 Years
Healthy volunteers
Accepted
Inclusion Criteria: 1. Being between the ages of 40-69 (Republic of Turkey Ministry of Health, 2020a). 2. Being a woman living in rural areas. 3. Being an illiterate woman. 4. Not being diagnosed with breast cancer. 5. Not being pregnant, breastfeeding or puerperant. 6. Accepting to participate in the study. 7. Absence of a mental illness. 8. No communication barriers Exclusion Criteria: 1. Not having completed the given training sessions 2. Having had problems with breast cancer before. 3. Having breast conserving surgery for any reason.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Burdur Mehmet Akif Ersoy University Burdur Turkey (Türkiye)

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06898229 on ClinicalTrials.gov ↗ ← All trials in Turkey