Study Stopped
lack of enrollment
Interventional Study Collecting Quantitative and Qualitative Data About Patient With Non Treated Cancer
DEREDIA
Determinants of the Consultation Delay in Cancers of the Upper Aero Digestive Tract
2 other identifiers
interventional
90
1 country
6
Brief Summary
This study aims to determine the impact of sociocognitive and emotional factors on the time of the initial consult
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Dec 2012
Longer than P75 for not_applicable
6 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 19, 2012
CompletedFirst Posted
Study publicly available on registry
July 23, 2012
CompletedStudy Start
First participant enrolled
December 1, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2014
CompletedStudy Completion
Last participant's last visit for all outcomes
February 1, 2017
CompletedMarch 13, 2026
March 1, 2026
1.8 years
July 19, 2012
March 12, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
time of first consultation
median time between date of symptoms appearance and date of first consultation
baseline
Secondary Outcomes (1)
identify variables associated with time of consultation
baseline
Study Arms (2)
questionnaires
ACTIVE COMPARATOR4 questionnaires to answer at baseline 45 minutes approx.
interview
EXPERIMENTALsemi directive interview 105 patients
Interventions
Eligibility Criteria
You may qualify if:
- age ≥ 18 years
- oral cavity cancer, oropharynx cancer, hypopharynx cancer, larynx cancer
- non treated cancer
- patient informed of his diagnosis
- speak fluent french
- patient covered by health insurance
- signed informed consent
- no speech troubles
- patient consents being recorded
You may not qualify if:
- history of cancer
- psychological history
- patient under guardianship
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (6)
Centre Hospitalier
Boulogne-sur-Mer, 62 231, France
Oscar Lambret Center
Lille, 59 020, France
Centre Hospitalier Régional et Universitaire - Hopital HURIEZ
Lille, 59 037, France
La Louviere Hospital
Lille, 59 042, France
Gray Center
Maubeuge, 59 600, France
Centre Médical Spécialisé du Littoral
Saint-Martin-Boulogne, 62280, France
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Veronique CHRISTOPHE, MDPhD
Lille 3 University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 19, 2012
First Posted
July 23, 2012
Study Start
December 1, 2012
Primary Completion
October 1, 2014
Study Completion
February 1, 2017
Last Updated
March 13, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share