Early Detection of Breast Cancer Among Syrian Women

NCT07056686 | Enrolling By Invitation DMC

• 1 other identifier: 01-05-2025
• Study Type: observational
• Target: 1,000
• Locations: 1 country
• Sites: 1

Brief Summary

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. 1.What is the level of awareness among women in this region regarding breast cancer symptoms and risk factors.
2. 2.How do women practice breast self-examination and professional screenings.
3. 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.

Conditions

Breast Cancer Detection

Outcome Measures

Primary Outcomes (1)

• Number of Participants with early signs of breast cancer

  From Participant enrolment to the end of the study at 2 weeks

Interventions

Mammogram DIAGNOSTIC_TEST

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.

Eligibility Criteria

• Age: 18 Years - 65 Years
• Sex: female
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Probability Sample

Study Population

Women in the middle reagon between 18-65 years old

Women aged 18 years and older residing in the middle region of Syria.

Contact the study team to discuss eligibility requirements. They can help determine if this study is right for you.

Sponsors & Collaborators

• Al-Hawash Private University: lead

Study Sites (1)

Al-Hawash Private University

Homs, 0000, Syria

Location

MeSH Terms

Interventions

Mammography

Intervention Hierarchy (Ancestors)

Radiography; Diagnostic Imaging; Diagnostic Techniques and Procedures; Diagnosis

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: CROSS SECTIONAL
• Target Duration: 12 Months
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: June 29, 2025
• First Posted: July 9, 2025
• Study Start: May 17, 2025
• Primary Completion: May 31, 2025
• Study Completion: July 30, 2025
• Last Updated: July 18, 2025

Record last verified: 2025-07

Data Sharing

• IPD Sharing: Will not share

Locations

SY (1)