Social Media-Based Education on Cancer Screening Awareness in Women: A Randomized Controlled Trial
The Effect of Social Media-Based Education on Women's Knowledge, Attitudes, and Health Literacy Regarding Cancer Screenings: A Randomized Controlled Trial
1 other identifier
interventional
132
1 country
1
Brief Summary
This randomized controlled study evaluated a social media-based educational program for women who had not previously participated in breast, cervical, or colorectal cancer screening. A total of 132 women aged 30-70 years were assigned to either a social media-based education group or a standard online education group. The social media-based program was structured according to the Social Ecological Model and delivered through closed WhatsApp and Instagram groups. The standard education group received two online educational sessions via Zoom. The study evaluated three primary outcomes: knowledge regarding cancer screenings, attitudes toward cancer screening, and self-reported digital health literacy. These outcomes were measured before the assigned educational program and four weeks after its completion. The study did not measure actual participation in cancer screening.
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 Jun 2025
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
First Submitted
Initial submission to the registry
April 15, 2025
CompletedFirst Posted
Study publicly available on registry
April 23, 2025
CompletedStudy Start
First participant enrolled
June 3, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2025
CompletedJuly 28, 2026
July 1, 2026
7 months
April 15, 2025
July 26, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Change in Cancer Screening Knowledge Score
Cancer screening knowledge was assessed using the 25-item Cancer Screening Knowledge Scale developed in Turkish. Items are answered as correct, incorrect, or "I do not know." Correct responses are scored as 1, and incorrect or "I do not know" responses are scored as 0. The total score ranges from 0 to 25, with higher scores indicating greater knowledge regarding breast, cervical, and colorectal cancer screenings.
Baseline and 4 weeks after completion of the assigned educational program
Change in Attitudes Toward Cancer Screening
Attitudes toward cancer screening were assessed using the 24-item Cancer Screening Attitude Scale developed in Turkish. Items are rated on a five-point Likert scale. The total score ranges from 24 to 120, with higher scores indicating a more positive attitude toward cancer screening.
Baseline and 4 weeks after completion of the assigned educational program
Change in Digital Health Literacy Level
Self-reported digital health literacy was assessed using the validated Turkish version of the 18-item Digital Health Literacy Instrument. The instrument includes six dimensions: information searching, evaluating reliability, determining relevance, navigating, adding self-generated content, and protecting privacy. Total and dimension scores are calculated as mean scores ranging from 1 to 4, with higher scores indicating higher self-reported digital health literacy.
Baseline and 4 weeks after completion of the assigned educational program
Study Arms (2)
Social Media-Based Education Group
EXPERIMENTALParticipants in this group received a Social Ecological Model-based educational program via closed WhatsApp and Instagram groups. During the eight-week program, 53 visual educational posters addressing breast, cervical, and colorectal cancer screenings and digital health literacy were shared. After completion of the scheduled poster-sharing period, four short reinforcement videos were also provided. A total of 57 educational materials were delivered.
Standard Education Group
ACTIVE COMPARATORParticipants in this group received two standard online educational sessions via Zoom, delivered one week apart. Each session lasted approximately 45-60 minutes and used a standardized slide presentation. The sessions covered breast, cervical, and colorectal cancer screenings, digital health literacy, and the use of digital health services.
Interventions
Participants received two standardized online educational sessions via Zoom, delivered one week apart. Each session lasted approximately 45-60 minutes. The sessions covered breast, cervical, and colorectal cancer screenings, preventive health information, digital health literacy, and the use of digital health services such as e-Nabız and MHRS. Participants were allowed to ask questions during the sessions; however, they did not receive the daily social media posts, repeated digital content, or continuous group interaction provided to the experimental group.
The intervention consisted of a Social Ecological Model-based educational program delivered through closed WhatsApp and Instagram groups. Fifty-three visual educational posters were shared during the eight-week program. The materials addressed breast, cervical, and colorectal cancer epidemiology, risk factors, symptoms, screening methods, healthy lifestyle behaviors, access to screening services, and digital health literacy. After the scheduled poster-sharing period, four approximately one-minute reinforcement videos covering breast cancer, cervical cancer, colorectal cancer, and digital health literacy were shared. The intervention therefore comprised a total of 57 educational materials.
Eligibility Criteria
You may qualify if:
- Female
- Aged 30-70 years
- Applied to Medipol Mega University Hospital in Istanbul between June and August 2025
- Had not previously undergone breast, cervical, or colorectal cancer screening
- Actively used both WhatsApp and Instagram
- Had access to a digital device and internet connection that enabled participation in the educational program
- Voluntarily agreed to participate and provided written informed consent
You may not qualify if:
- Previous diagnosis of any type of cancer
- Previous participation in any breast, cervical, or colorectal cancer screening procedure
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Emine Erginlead
- Saglik Bilimleri Universitesicollaborator
Study Sites (1)
Medipol Mega University Hospital
Istanbul, 34214, Turkey (Türkiye)
Study Officials
- PRINCIPAL INVESTIGATOR
Şerife Çınar, PhD Candidate, Midwife
Medipol University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Associate professor
Study Record Dates
First Submitted
April 15, 2025
First Posted
April 23, 2025
Study Start
June 3, 2025
Primary Completion
December 31, 2025
Study Completion
December 31, 2025
Last Updated
July 28, 2026
Record last verified: 2026-07
Data Sharing
- IPD Sharing
- Will not share
No prospective plan was established for sharing individual participant data. The study contains potentially identifiable participant information, and public IPD sharing was not incorporated into the study's original data-management procedures. Study findings will be reported in aggregate form.