Early Detection of Breast Cancer Among Syrian Women
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Mammogram.
- Who it may be relevant to
- Registry conditions: Breast Cancer Detection. Basic parameters: 18 years — 65 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Syria
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Early Detection of Breast Cancer Among Women in the Middle Region of Syria
Overview
The goal of this observational study is to evaluate breast cancer awareness, screening practices, and barriers to early detection among women in the middle region of Syria. The main questions it aims to answer are: 1. What is the level of awareness among women in this region regarding breast cancer symptoms and risk factors. 2. How do women practice breast self-examination and professional screenings. 3. What barriers prevent women from seeking early detection and treatment? Participants will complete a survey assessing their knowledge, behaviors, and challenges related to breast cancer screening. The findings will inform public health interventions to improve awareness and early detection practices.
Interventions
- Diagnostic test Mammogram
Each patient will undergo a mammogram and echo of the breast used to detect early signs of cancer, such as tumors or calcifications, before symptoms appear.
Primary outcome measures
- Number of Participants with early signs of breast cancer [Time frame: From Participant enrolment to the end of the study at 2 weeks]
Eligibility criteria
Women aged 18 years and older residing in the middle region of Syria.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Cohort
Study locations
Syria · 1 center
- Al-Hawash Private University — Homs
Identifiers
NCT: NCT07056686 · 01-05-2025