Actively Recruiting
Implementing a Systemic Screening for Tuberculosis Disease in High-risk Groups in the Barcelona Area
Led by Fundació Institut Germans Trias i Pujol · Updated on 2024-11-29
3000
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
F
Fundació Institut Germans Trias i Pujol
Lead Sponsor
C
Catalan Public Health Agency
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are conducting a screening study to identify people at high risk of active pulmonary tuberculosis (TB) in the Barcelona area. The study focuses on vulnerable groups such as war refugees, migrants, and individuals living in socio-economically deprived neighborhoods. The goal is to detect TB symptoms early and refer those who screen positive for further medical evaluation. Participants who qualify and provide verbal consent will first attend an educational talk about TB. They will then be interviewed and screened for symptoms like cough, blood in sputum, fever, weight loss, night sweats, and chills lasting more than two weeks. Those who show symptoms will be referred to a hospital for additional examinations, including chest X-rays and laboratory tests. During the study, researchers will track how many individuals screen positive for TB symptoms and how many are ultimately diagnosed. They will also analyze the cost-effectiveness and time spent during the screening process. The study aims to improve early detection and management of TB in high-risk populations through this observational approach.
CONDITIONS
Brief Title
A Systemic Screening for TB Disease in High-risk Groups in Barcelona
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Belonging to a population at high risk for tuberculosis (TB)
You will not qualify if you...
- Not belonging to a population at high risk for tuberculosis (TB)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 1 month
Participants who screen positive for TB symptoms undergo diagnostic testing including a chest X-ray and laboratory tests to confirm the presence of tuberculosis.
1 to 2 visits depending on diagnostic procedures
Duration - Not specified
Participants diagnosed with TB may be monitored over time as part of observational follow-up.
Additional visits as needed
Trial Site Locations
Total: 1 location
1
IGTP
Badalona, Spain, 08916
Actively Recruiting
Research Team
C
Cristina Vilaplana, MD, PhD
N
Nino Gogichadze, MD, MsC
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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