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Trial Title: The Effect of Web-Assisted Peer Education for Early Diagnosis of Breast Cancer on Health Beliefs, Knowledge Levels and Breast Self-Examination in University Students

NCT ID: NCT06112158

Condition: University Students
Breast Self-examination
Health Education

Conditions: Official terms:
Breast Neoplasms

Conditions: Keywords:
Breast self-examination
Health Education
University students
Breast cancer

Study type: Interventional

Study phase: N/A

Overall status: Recruiting

Study design:

Allocation: Randomized

Intervention model: Parallel Assignment

Intervention model description: Two groups with randomized controlled trial

Primary purpose: Screening

Masking: Single (Participant)

Masking description: Web-supported and face-to-face training on breast cancer information and screening will be provided to the experimental group.and outcome assessments will be performed by a investigator who was blinded to group allocation.

Intervention:

Intervention type: Behavioral
Intervention name: Education Intervention
Description: The BSE training program for the early diagnosis of breast cancer will be offered to students in two ways: face-to-face and via web support. Content of training Session 1: Topics such as the structure of the breast, the definition of breast cancer, its prevalence, risk factors and symptoms Session 2: Teaching the importance of early diagnosis in breast cancer, the importance and benefits of BSE, the technique of performing BSE, the obstacles to the application of BSE. Session 3: Teaching the risk factors that cause breast cancer. Session 4: Discussion of case reports of patients diagnosed with breast cancer. Supporting education with web support
Arm group label: Education Intervention

Summary: The aim of this study was to examine the effect of web-supported peer education on health beliefs, knowledge levels and breast self-examination in university students.

Detailed description: In line with the general purpose of the study, an experimental design will be used in the study. The population of this study consists of female students of Ankara Medipol University. Considering that there may be dropouts from the study in line with the determined sample size, 200 students (intervention; n=100, control; n=100) who were excluded from the exclusion criteria and who agreed to participate in the study were planned to constitute the study group. Hypotheses of the Research Between the experimental group and the control group, which received peer education on breast cancer and Breast Self-Examination (BSE); H1a1: There is a difference in terms of the sensitivity subscale score average. H1b1: There is a difference in terms of the mean score of the seriousness/importance subscale. H1c1: There is a difference in terms of the average score of the benefit perception subscale. H1d1: There is a difference in terms of the average score of the obstacle perception subscale. H1e1: There is a difference in terms of the mean score of the trust subscale. H1f1: There is a difference in terms of the health motivation subscale score average. H2a1: There is a difference in terms of the average knowledge score. H3a1: There is a difference in terms of performing breast self-examination.

Criteria for eligibility:
Criteria:
Inclusion Criteria: - Young women who do not have any diagnosis of cancer or breast cancer - who have no communication barriers - who are not pregnant or breastfeeding - who volunteer to participate in the study Exclusion Criteria: - Participants with a previous cancer diagnosis - CHCMM training and who were absent for more than two sessions in the intervention group

Gender: Female

Minimum age: N/A

Maximum age: N/A

Healthy volunteers: Accepts Healthy Volunteers

Locations:

Facility:
Name: Ankara Medipol Unıversty

Address:
City: Ankara
Zip: 06000
Country: Turkey

Status: Recruiting

Contact:
Last name: Esra Özer, Asisst. Prof.

Phone: +905433630475
Email: esra.ozer@ankaramedipol.edu.tr

Investigator:
Last name: Yeşim Çetinkaya, Lecturer
Email: Sub-Investigator

Start date: March 13, 2024

Completion date: June 30, 2024

Lead sponsor:
Agency: Esra ÖZER
Agency class: Other

Collaborator:
Agency: Ankara Medipol University
Agency class: Other

Source: Ankara Medipol University

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT06112158

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