Web-Based Education Program and Educational Booklet Developed on Cervıcal Cancer
The Effect of a Web-Based Education Program and Educational Booklet Developed on Cervıcal Cancer on Women's Prevention Methods
1 other identifier
interventional
128
1 country
1
Brief Summary
Cervical cancer is the fourth most common cancer type among women worldwide and ranks ninth in Turkey, making it the second most common gynecological cancer. The prevention of cancer heavily relies on identifying risk factors, implementing preventive measures, and early diagnosis. Cervical cancer is associated with high-risk Human Papilloma Virus (HPV) infections, transmitted primarily through sexual contact, accounting for 99.7% of cases. Risk-enhancing factors include early sexual activity, poor hygiene, low socioeconomic status, and immunosuppressive conditions. The World Health Organization (WHO) launched the "Cervical Cancer Elimination Program" to address this public health issue, aiming for 90% of girls to be vaccinated against HPV by age 15, 70% of women aged 35-45 to be screened, and 90% of women diagnosed with cancer to have access to treatment by 2030. The low participation rate in cervical cancer screening programs in Turkey highlights the urgent need to increase public awareness. Web-based education is an effective tool for promoting health behaviors and increasing awareness. Its cost-effectiveness, ability to reach large audiences, and easy accessibility make it a valuable resource in healthcare. Studies in the literature demonstrate that web-based and video-based education significantly enhance cervical cancer awareness and encourage pap smear test uptake. This study developed a web-based education program and an educational booklet on cervical cancer, based on the Health Belief Model, to evaluate their impact on women's knowledge, attitudes, and behaviors. The study aims to contribute to the dissemination of cervical cancer prevention methods and enrich the existing literature.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started May 2024
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 29, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 31, 2024
CompletedFirst Submitted
Initial submission to the registry
November 21, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
November 21, 2024
CompletedFirst Posted
Study publicly available on registry
November 26, 2024
CompletedNovember 26, 2024
November 1, 2024
3 months
November 21, 2024
November 25, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
The Effect of a Web-Based Education Program and Educational Booklet Developed on Cervical Cancer on Women's Prevention Methods
To develop a web-based education program and an educational booklet on cervical cancer, and to assess the effectiveness of this program and booklet in improving women's knowledge, attitudes, and behaviors regarding cervical cancer prevention. The evaluation will be based on pre- and post-intervention surveys measuring changes in participants' understanding of cervical cancer, their attitudes toward screening and prevention, and their behaviors related to cervical cancer prevention practices.
1.5 year
Study Arms (1)
Web-Based Education Group
EXPERIMENTALWeb-Based Education Group
Interventions
The Effect of a Web-Based Education Program and Educational Booklet Developed on Cervıcal Cancer on Women's Prevention Methods
Eligibility Criteria
You may qualify if:
- Being between the ages of 30-65,
- Having never had a cervical cancer screening before,
- Having received training on cervical cancer,
- There is no obstacle to answering the questions physically, mathematically or spiritually,
- Having internet access,
- Being able to use a computer and/or tablet effectively,
- Academicians working in health programs,
- Healthy female academics who did not agree to participate in the research,
- Being able to use a computer
You may not qualify if:
- The emergence of any health problem that prevents the person from continuing the research,
- Not completing any of the required forms,
- Those who give up participating in the study at any stage of the study
- Do not visit 80% of the tabs in the web training program,
- Those who have never read the training booklet will be excluded.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Istanbul University - Cerrahpasa
Avcılar, 34320, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Ebru Sen
Istanbul University - Cerrahpasa
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Phd Student - Lecturer
Study Record Dates
First Submitted
November 21, 2024
First Posted
November 26, 2024
Study Start
May 29, 2024
Primary Completion
August 31, 2024
Study Completion
November 21, 2024
Last Updated
November 26, 2024
Record last verified: 2024-11