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Clinical Trial Summary

The main objective is to assess the feasibility of collecting and implementing a multidimensional evaluation in a sample of patients with a mild to severe traumatic brain injury (TBI) and their relatives, evaluated at 6 months (primary outcome), and at 12 then 18 months post-injury (secondary outcomes).


Clinical Trial Description

The study aims to assess the feasibility of collecting multidimensional outcomes of patients with traumatic brain injury, taking into account the patient-relative dyad. However, this multidimensional assessment may pose enormous problems of feasibility during the follow-up: loss of the patient's pathway, moderate acceptance by patients and relatives, difficulties of remote assessment sometimes carried out several times.... All these factors can affect the methodological quality of the evaluation of patient outcomes, with measurement and reporting biases influencing the results of biomedical trials. In order to improve the quality of clinical research in this field, it is therefore essential to fully appreciate the factors that facilitate or, on the contrary, hinder high-quality longitudinal follow-up. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06194071
Study type Observational
Source Nantes University Hospital
Contact Raphaël CINOTTI, Pr
Phone +33(0)240084731
Email raphael.cinotti@chu-nantes.fr
Status Recruiting
Phase
Start date November 11, 2023
Completion date May 2025

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