MedTrace Logo

Validation of an Ecological Organization and Problem Solving Test (TEM-PRO) in Vocational Rehabilitation

NCT04087486 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 40

Last updated 2022-11-01

No results posted yet for this study

Summary

Standard neuropsychological evaluations after severe TBI (traumatic brain injury) often minimizes the executive deficits, these latter are known to seriously impair return to work. Therefore, we developed an ecological organization and problem-solving test in a vocational setting called the TEM-PRO. The test consists of 4 activities of variable complexity, collection and redaction of information and demands to follow well defined rules.

Conditions

  • TBI (Traumatic Brain Injury)

Interventions

DIAGNOSTIC_TEST

Implementation of a behavioural test for patients with TBI

The following data will be collected: (1) sociodemographic variables (2); clinical and psychological data; (3) functional tests (neuropsychological testing, TEM version CRR and TEM-PRO). On day one, patients will undergo standard neuropsychological tests and questionnaires listed hereafter, which are commonly used in the clinical practice at the CRR. * The Patient Competency Rating Scale (PCRS) * TEM (Multiple errands test) * GREFEX * 5 POINTS TEST * TAP 2.3 * Behavioral Assessment of the Dysexecutives Syndrome (BADS) On day two, the patients will perform the TEM-PRO test ambulatory in our vocation rehabilitation unit. "Predictors" variables will be collected before testing: Sociodemographic: age, sex, education, marital status, mother language, time since TBI, severity of the TBI (moderate or severe), type of lesion (contusion, diffuse axonal injury grade 1-3, ischemic or other complications), history of TBI, stroke or meningitis.

Sponsors & Collaborators

  • Clinique Romande de Readaptation

    lead NETWORK

Principal Investigators

  • Andreas Mühl, MD · Clinique romande de réadaptation

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-01-01
Primary Completion
2022-07-31
Completion
2023-03-30

Countries

  • Switzerland

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04087486 on ClinicalTrials.gov