Clinical trial Recruiting at 1 site Observational

Glioblastoma in Réunion: an epidemiological and socio-anthropological look at patients and care

Official title: Diffuse Gliomas in Reunion Island: Establishment of an Epidemiological, Clinical-biological and Socio-anthropological Cohorte

Run by Centre Hospitalier Universitaire de la Réunion · NCT07865195 · Data updated 2026-11-12

A large group of adults with diffuse gliomas in Réunion is being studied to understand how biology, culture, and health care pathways affect diagnosis and treatment.

More Glioblastoma trials

Quick facts

Study typeObservational
SexAll
Enrollment214 (estimated)
SponsorCentre Hospitalier Universitaire de la Réunion
Academic / other
Drugs / interventionsradiation
Locations1 site (Saint-Pierre)
StatusRecruiting
StartedApril 7, 2025
Main results expectedApril 7, 2028
Study endsNovember 7, 2028
Registry record updatedOctober 8, 2026
Trial IDNCT07865195 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (18+) residing in Réunion with a histological diagnosis of incident diffuse glioma since January 1, 2018, who are able and willing to participate.

Probably not a fit

Participants may not directly benefit personally; the study aims to improve understanding and care strategies for future patients.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a mixed-methods study that combines retrospective and prospective data collection on adults with incident diffuse gliomas diagnosed since 2018 in Réunion. The project uses epidemiological data plus qualitative interviews to explore socio-cultural factors, care pathways, and patient experiences. Data will come from medical records and direct interviews with patients and healthcare professionals, aiming to map population characteristics, treatment patterns, and gaps in care. The study is led by the Centre Hospitalier Universitaire de la Réunion and involves collaboration with local clinicians and researchers. No interventional procedures are involved; the focus is observational and descriptive.

Why it matters

Potential benefit: Findings could clarify regional care gaps and inform efforts to tailor glioma care pathways on Réunion Island.

How similar studies have gone: Similar observational cohorts have provided valuable epidemiological and socio-anthropological insights in other regions; this study adapts that approach to Réunion’s context.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

Quantitative study (retrospective and prospective components):

Patients aged 18 and over:

* With a histological diagnosis of incident diffuse glioma since January 1, 2018
* Residing in Réunion at the time of diagnosis,
* Having been informed about the study procedures
* Having agreed to participate in the study

Socio-anthropological study (prospective component):

Patients:

* Meeting the inclusion criteria for the prospective quantitative study and agreeing to participate in the qualitative component,
* Speaking French. • Able to participate in a face-to-face interview

Healthcare Professional:

* Professionals involved in the care of patients with brain tumors (medical, paramedical, social care, support care, etc.) who have agreed to participate in the study
* The healthcare professionals concerned will be general practitioners, neurosurgeons, neurologists, radiation oncologists, medical oncologists, home healthcare physicians, palliative care physicians, pathologists, nurses responsible for diagnosis and follow-up, psychologists, social workers, and dietitians.

Exclusion Criteria:

Regarding the quantitative study:

Patient:

Refusing to participate in the quantitative study Having a recurrent diffuse glioma Person deprived of their liberty and judgment by judicial or administrative decision, and person subject to a legal protection measure: guardianship or curatorship, under judicial protection, under legal guardianship, etc.)

Regarding the socio-anthropological study:

Patient:

Refusing to participate in the qualitative study Does not speak French Having serious somatic or mental health problems incompatible with the interview Healthcare professionals: Refusing to participate in the study

Where it's running

  • Mélanie BEGORRE
    Saint-Pierre, Reunion
    Recruiting

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.