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Quality of Life in Traumatic Brain Injury Patients

G

General Administration of Military Health, Tunisia

Status

Enrolling

Conditions

All Adult Patients Admitted to theHMPIT ICU for Management of Head Trauma

Treatments

Other: quality of life

Study type

Observational

Funder types

NETWORK

Identifiers

Details and patient eligibility

About

The aim of this study is to describe the quality of life of CT patients in our study, at least 6 months after the occurrence of the trauma. This assessment is related to the patient's degree of sequelae, using the GOSE scale.

Full description

The assessment of patients quality of life would appear to be a particularly relevant tool in the ongoing drive to improve the quality of care. Thus, we should no longer simply assess how patients "should feel", based on objective biomedical criteria, but how they actually "perceive" themselves, based on subjective criteria.

This is particularly true in the case of traumatic brain injury , which is a high-incidence pathology with significant morbidity and mortality consequences that can lead to permanent sequelae . While research over the past 30 years has focused on the neuropsychological and functional outcomes of this event, less is known about the views of head injury survivors and their families on their quality of life, subjective well-being and related factors.

The aim of this study is to describe the quality of life of CT patients at least 6 months after the trauma. This assessment is related to the patient's degree of sequelae, using the Glasgow Outcome Scale Extended GOSE.

Enrollment

100 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

All adult patients (age 18 or over) admitted to the HMPIT intensive care unit for management of head trauma (isolated or as part of a polytrauma).

Exclusion criteria

Patients lost to follow-up after discharge. Incomplete ICU medical records. Patients or their families who refused to participate in the study.

Trial design

100 participants in 1 patient group

A bras actif
Treatment:
Other: quality of life

Trial contacts and locations

2

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Central trial contact

Aicha REBAI, FR

Data sourced from clinicaltrials.gov

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