Breast and Cervical Cancer Awareness Training in Visually Impaired Women

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age40+
SponsorMarmara University

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 volunteers

Qualifiers

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

Design model

Parallel

Treatments tested in this trial

  • Cancer Screening Awareness Education for Visually Impaired Women

    Behavioral

    This 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

74 Participants
are divided into 2 treatment groups
Group A: Cancer Screening Awareness Education (Intervention Group)Experimental treatment 1 intervention
Group B: No Education (Control Group)No intervention 0 interventions

Trial outcomes

Primary outcomes

1

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).

Time frame
Post-test (immediately after the training), follow-up test (3 months later).

Secondary outcomes

1

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).

Time frame
Pre-test (before education), post-test (immediately after education), and follow-up test (3 months later)

Other outcomes

Sponsors and contacts

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