Characterisation of MNEsic Involvement in Patients With Obesity.

NCT07796932 — Not yet recruiting, 150 participants, University Hospital, Bordeaux

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RegistryNCT07796932, acronym MNEMOB
StatusNot yet recruiting
Study typeObservational
Enrollment150 (Estimated)
SponsorUniversity Hospital, Bordeaux (Other)
ConditionsObesity (Disorder)
InterventionsRMI and Questionnaires (Other)
Datesstart 2027-01-01 (estimated), primary completion 2030-02-01 (estimated), completion 2030-02-01 (estimated), first posted 2026-09-01, last updated 2026-09-01

Related Papers Related Patents Related Grants Related Experts
All trials for Obesity (Disorder) All trials of RMI and Questionnaires

-Summary

The aim of the study is therefore to characterise memory impairment in a middle-aged population with obesity and to clarify the role of inflammation in obesity-related memory impairment.

The hypothesise that, as in an elderly population, neurological and memory impairment in a population of middle-aged obese individuals is heterogeneous, with varying levels of memory impairment characterised by neuropsychological test results. This heterogeneity in neuropsychological tests may be linked to markers of inflammation and brain imaging biomarkers identified previously in the litterature.

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+Arms and interventions

ArmTypeInterventionsDescription
Magnetic Resonance Imaging, CANTAB questionnairesOther: RMI and Questionnaires
  • RMI and Questionnaires (Other): Magnetic resonance imaging (MRI) will collect anatomical information (3D T1 weighted images) to compute the volumes of the hypothalamus, hippocampus and the other brain parcels. Executive functions using the CANTAB tests and validated questionnaires will be performed.

+Outcome measures

Primary outcomes

  • Memory function characteristic [37 months after inclusion day]: The main objective is to characterise memory function in a population of middle-aged individuals suffering from obesity using the CANTAB Paired Associates Learning (PAL) test.

+Eligibility

Sex: All, ages: 30 Years to 50 Years

Inclusion Criteria:

* Patients suffering from obesity with a BMI between 30 and 45 kg/m²
* Patients aged between 30 and 50 receiving educational care during the week at the CSO (Endocrinology, Diabetology and Nutrition Department) of the Bordeaux University Hospital.
* Right-handed patients
* Persons affiliated with or beneficiaries of a social security scheme.
* Free, informed and express consent

Exclusion Criteria:

* Patients currently undergoing treatment with neuroleptics or who have stopped treatment within the last 3 months.
* Pregnant or breastfeeding patients
* Known current or past neurological disease
* Proven depressive syndrome treated
* Patients with type 1 or type 2 diabetes
* Uncontrolled dysthyroidism
* MMS< 25
* Patients with proven genetic obesity
* Contraindication to MRI
* Chronic use of NSAIDs or corticosteroids
* Loss of 5% of body weight in the 3 months prior to the study
* Acute infection
* Persons deprived of their liberty by judicial or administrative decision
* Adults subject to legal protection measures (guardianship, curatorship, judicial protection)

+Investigators

  • Daniela COTA, Pr, Study director, INSERM u1215