Psychometric Validation of the MQOL-FR and Descriptive Assessment of Quality of Life in Patients With Meningiomas

Starting soon

Conditions studied: Intracranial Meningioma, Meningioma, Health-related Quality of Life

In brief

This non-interventional study aims to validate the French version of a meningioma-specific quality-of-life questionnaire (MQOL-FR) and to describe health-related quality of life in adults diagnosed with an intracranial meningioma. Participants will be invited to complete online questionnaires through a secure REDCap link. After reading the study information and recording their non-opposition, participants will complete: (1) MQOL-FR (meningioma-specific), (2) EQ-5D-5L (generic health-related quality of life), and (3) FACT-Br (brain tumor-specific quality of life). The questionnaire session takes approximately 30-45 minutes and can be completed in more than one sitting using a REDCap access code. There is no additional visit and no change in usual care. The study will recruit adults (≥18 years) with a meningioma diagnosis based on imaging and/or confirmed by surgery, through the GHU Paris-Sainte-Anne neurosurgery clinic and through patient/community networks. The goal is to obtain 100 fully completed MQOL-FR questionnaires suitable for psychometric analyses.

Key facts

Study ID

NCT07376473

Run by

Centre Hospitalier St Anne

People needed

238

Starts

2026-02-02

Expected to finish

2026-09-02

Last updated by the study team

2026-02-03

Who can join

Age: 18 and older, up to 60. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Inclusion Criteria:
• Age ≥ 18 years
• Diagnosis of intracranial meningioma on imaging and/or confirmed by surgery

You may not qualify if…

• Pregnant or breastfeeding
• Individuals deprived of liberty by judicial/administrative decision or under compulsory psychiatric care
• Insufficient French language proficiency/comprehension
• Unable to complete the questionnaires independently
• Unable to express non-opposition to participation

Full record on ClinicalTrials.gov

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