Women on Breast Cancer Health Belıefs and Screenıng Behavıors
NCT ID: NCT05677737
Last Updated: 2023-07-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
165 participants
INTERVENTIONAL
2022-08-15
2023-07-15
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effect of Education on Breast Cancer Fear and Health Beliefs
NCT06543147
The Effect of Breast Cancer Screening Training
NCT05723237
The Effect of Health Education on Breast Cancer
NCT06022900
A Quasi-Experimental Study to Improve Breast Cancer Awareness Among University Students
NCT07118969
The Effect of Animation-Based Education on Menopausal Women's Attitudes, Behaviors, and Screening Test Participation Regarding Breast Cancer
NCT07042737
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
PREVENTION
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Experimental
In the study, the women in the experimental group will be trained every two weeks for 6 weeks.
Education
Educational program; It will be applied to the individuals in the experimental group for an average of 40 minutes in a time period they are suitable through the online platform prepared for the individuals in the experimental group in a three-month period. The literature will be scanned and appropriate educational materials will be created, and videos will be used to support education.
Educational program During the first interview, the individuals in the experimental group will be introduced to the online platform, their entrance will be provided, they will be informed about how to follow the trainings, and sample applications will be made.
Six main topics will be covered in the training program and will be completed every two weeks in three months.
Control
No intervention will be applied to the control group.
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Education
Educational program; It will be applied to the individuals in the experimental group for an average of 40 minutes in a time period they are suitable through the online platform prepared for the individuals in the experimental group in a three-month period. The literature will be scanned and appropriate educational materials will be created, and videos will be used to support education.
Educational program During the first interview, the individuals in the experimental group will be introduced to the online platform, their entrance will be provided, they will be informed about how to follow the trainings, and sample applications will be made.
Six main topics will be covered in the training program and will be completed every two weeks in three months.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Being literate,
* Computer can be used,
* Internet is accessible,
* Not getting breast cancer before,
Exclusion Criteria
* Having a history of breast cancer in first degree relatives
* Those who did not attend all of the online trainings in the experimental group
18 Years
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Ataturk University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
NİHAN TÜRKOĞLU
Assist Prof.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Aslı Sis Çelik, Assoc. Prof.
Role: STUDY_CHAIR
Ataturk University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Ataturk Unıversity
Erzurum, Yakutiye, Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
nihan25
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.