Ireland
--:--IST
Active, not recruiting Observational

Individual Factors Associated With Care Pathways Delays in Breast Cancer in Hauts-de-France.

NCT07475325 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2026-04-20
Last updated
2026-05-12

Condition(s) studied

Breast CancerInvasive Breast Carcinoma

Study summary

Women in the Hauts-de-France region show higher breast cancer mortality despite no overall higher incidence, suggesting differences in the care pathway. This multicenter study will describe the overall time from the first warning sign to initiation of the first treatment, and will break down this delay into three consecutive intervals (symptoms to mammography, mammography to biopsy, biopsy to first treatment). Participants will complete a one-time questionnaire (up to 1 hour, with assistance if needed), and clinical data will be extracted in a standardized way from medical records (key dates and tumor characteristics). A random sample of 10% of incident breast cancer cases identified by each hospital information department will be used to ensure balanced geographic representation across 38 centers. The study will also explore how individual and contextual factors (psychological, behavioral, socio-demographic, access to care, communication) are associated with each time interval, and exploratory analyses will assess links with severity (metastases and prognostic score).

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Female, age ≥ 18 years. * Confirmed invasive breast carcinoma. * Diagnosis in 2024 (and/or \< 12 months at inclusion depending on center organization). * Affiliated with the French social security system. * Resident of Hauts-de-France since diagnosis. * Information provided and non-opposition documented (MR-003). Exclusion Criteria: * Male breast cancer. * Other histologies (phyllodes tumor, sarcoma, lymphoma). * Pure ductal carcinoma in situ (in situ only). * Personal history of breast cancer (including in situ). * Non-French-speaking. * Person deprived of liberty.

Primary outcome measure(s)

  • Total time from first warning sign to initiation of first treatment. — One-time assessment using patient-reported dates and medical record dates at inclusion (single questionnaire session + record extraction). Questionnaire time : around 1 hour

Trial sites (34)

FacilityCityRegionStatus
Clinique Ste Isabelle Abbeville France
CHU Amiens Amiens France
Clinique Victor Pauchet Amiens France
Centre Marie Curie Arras France
Hôpital privé Les Bonnettes Arras France
CH Beauvais Beauvais France
Centre Pierre Curie Beuvry France
CH Bethune Béthune France
CH Boulogne Boulogne France
CH Calais Calais France
CH Chauny Chauny France
Centre de Radiothérapie de Compiègne Compiègne France
Polyclinique St Côme Compiègne France
CH Compiègne Compiègne France
Clinique de Flandre Coudekerque-Branche France
Centre de Radiothérapie de Creil Creil France
Centre Leonard de Vinci Dechy France
Polyclinique de la Clarence Divion France
Institut Andrée Dutreix Dunkirk France
CH Dunkerque Dunkirk France
Polyclinique d'Hénin-Beaumont Hénin-Beaumont France
CH Lens Lens France
Centre Oscar Lambret Lille France
Hôpital privé Le Bois Lille France
Hôpital St Vincent Lille France
CHU Lille Lille France
Centre Gray Maubeuge France
CH Roubaix Roubaix France
CH St Quentin Saint-Quentin France
CH Soissons Soissons France
Clinique de la Victoire Tourcoing France
CH Tourcoing Tourcoing France
Clinique des dentellières Valenciennes France
CH Valenciennes Valenciennes France
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07475325 on ClinicalTrials.gov ↗ ← All trials in France