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Clinical Trial Summary

The overall objective is to assess the acceptability and feasibility of offering personalized breast cancer (BC) screening.

The specific objectives are: 1) To design an information system; 2) To evaluate the barriers and facilitators of the coordination of health care services and the screening program; 3) To develop a proof of concept of personalized screening; and 4) To evaluate cost-effectiveness.

Methodology:

1. Prototype information system with basal and longitudinal variables relevant to a personalized screening system;

2. Qualitative study with focus groups and survey. The attitude and acceptability on a sample of 210 health professionals will be assessed;

3. Prospective observational study, for proof of concept. Participants will be professionals working in Primary Care, Population Breast Screening Program, or Hospital Breast Unit. It will include 385 women, aged 40-50 from the city of Lleida. Various indicators of acceptability and feasibility will be assessed in women and health professionals;

4. Probabilistic analytical models will be used to evaluate cost-effectiveness.

The present protocol addresses the specific objective number 3, the proof of concept of personalised screening.

Expected results: The investigators expect to provide valuable and necessary information for the design of personalized screening.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03791008
Study type Interventional
Source Institut de Recerca Biomèdica de Lleida
Contact Montserrat Rue, PhD
Phone +34659412636
Email montse.rue@gmail.com
Status Recruiting
Phase N/A
Start date January 30, 2019
Completion date December 2020

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