About this trial
This quasi-experimental study aims to determine whether a breast and cervical cancer awareness training program can increase participation in cancer screening among women with visual impairments. The study also aims to identify barriers to screening and improve knowledge about cancer risk factors and screening methods. The main questions this study will address are:
* Does the training increase the rate at which women with visual impairments attend cancer screening appointments? * Does the training improve participants' knowledge about breast and cervical cancer?
Participants will:
* Receive training on breast and cervical cancer risk factors and screening methods. * Learn how to apply to the Cancer Early Diagnosis, Screening, and Training Center. * Be encouraged to attend cancer screening during the study period. * Have knowledge and screening status assessed before the training, immediately after, and three months later.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Women with only a visual impairment (congenital or acquired)
Able to communicate, speak, and understand Turkish
Voluntarily agree to participate in the study
Over the age of 40
Disqualifiers
Diagnosed with breast or cervical cancer
Under the age of 40
Have not had sexual intercourse before
Have undergone screening for at least one of these two cancer types (breast or cervical) within the last year
Trial design
Parallel
Treatments tested in this trial
Cancer Screening Awareness Education for Visually Impaired Women
BehavioralThis intervention is an educational program designed to increase awareness among visually impaired women regarding breast cancer, cervical cancer, and colorectal cancer screenings. The training covers cancer risk factors, screening methods, the application process for Cancer Early Diagnosis, Screening and Training Centers (KETEM), communication methods, and recommended screening intervals. Following the training, participants will receive individual counseling to support them in scheduling screening appointments. A pre-test, post-test, and follow-up test will be administered during the intervention process.
Treatment groups
Trial outcomes
Primary outcomes
Change in Cancer Screening Uptake Rate
Change in the percentage of visually impaired women who undergo breast and cervical cancer screening at Cancer Early Diagnosis, Screening, and Training Centers (KETEM) after the educational intervention. * Scale: Not applicable (measured as percentage). * Range: 0% - 100%. * Interpretation: Higher percentages indicate a better outcome (higher screening participation).
Secondary outcomes
Change in Knowledge Scores
Change in scores regarding breast and cervical cancer risk factors and screening methods. * Scale Title: Cancer Screening Knowledge Scale (Öztürk \& Uyar, 2023). * Range: 0 - 25 points. * Interpretation: Higher scores indicate better knowledge. * Assessment Points: Pre-test (before education), post-test (immediately after education), follow-up test (3 months later).
Sponsors and contacts
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