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Recruiting NCT07044076

Translation and Validation of the MQOL Self-questionnaire Into French for Assessing Quality of Life in Patients With Meningiomas

Observational Quality of Life Meningioma

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Quality of life.
Who it may be relevant to
Registry conditions: Quality of Life, Meningioma. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Meningiomas, which account for about 40% of primary central nervous system tumors, have significant psychological and social impacts, even without treatment. Their effect on quality of life is often underestimated and poorly documented. There is one validated questionnaire (MQOL) but it has not yet been translated into French. The project involves two phases: first, translating and linguistically validating the MQOL into French; second, scientifically validating the questionnaire with 50 meningioma patients using established scales (EQ-5D, Karnofsky, FACT-Br) to ensure its reliability and internal consistency.

Interventions

  • Other Quality of life
    The four questionnaires (MQOL, EQ-5D, Karnofsky, and FACT-Br) will be sent to patients online using the secure online platform Redcap.

Primary outcome measures

  • meningioma-specific quality-of-life questionnaire [Time frame: 1 month]

Eligibility criteria

Inclusion criteria

  • Patient aged 18 years or older
  • Diagnosis of intracranial meningioma confirmed by imaging or surgery

Exclusion criteria

  • Pregnant or breastfeeding women (Article L1121-5)
  • Patients deprived of liberty by judicial or administrative decision, as well as individuals undergoing psychiatric care (Article L1121-6)
  • Patients not fluent in French or with poor understanding of the language
  • Inability to refuse participation in the study

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Study design

Observational model
Other

Study locations

France · 1 center
  • GHU Paris -Psychiatrie & Neurosciences — Paris

Identifiers

NCT: NCT07044076 · D25 - P003

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗