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Evaluation of a Virtual Reality-based Version of the Multiple Errands Test in Alcohol Use Disorder (EVIMETAL)

18. maj 2026 opdateret af: Hôpital le Vinatier

Evaluation of a Virtual Reality-based Version of the Multiple Errands Test for the Assessment of Executive Functions in Alcohol Use Disorder

The goal of this study is to validate the virtual version of the Multiple Errands Test (V-MET) as a tool for assessing executive functions in patients with alcohol use disorder (AUD).

More specifically, the project aims to:

  1. evaluate if the performance in the virtual version of the test is related to the performance in the original test in patients with AUD.
  2. establish whether the virtual version of the test is sensitive enough to detect patients with or without an executive function deficit.

All participants will perform the original version (in a real-life supermarket) and the virtual version of the test (in a virtual reality environment).

Performance in the two versions of the test will be compared. Participants will also complete a battery of neuropsychological tests and questionnaires.

Studieoversigt

Detaljeret beskrivelse

The project aims to validate the virtual version of the Multiple Errands Test (V-MET) as a tool for assessing executive function in patients with alcohol use disorder (AUD), in comparison to the original test (MET), by:

  1. establishing the ecological validity of the V-MET: a high correlation between performance on the MET and performance on the V-MET (total number of errors) in patients with TUAL and executive dysfunction.
  2. establishing the sensitivity of the V-MET (to executive dysfunction): significant difference between V-MET performance in patients with an AUD and executive dysfunction versus (a) patients without executive dysfunction and (b) "healthy" volunteers

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

90

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Undersøgelse Kontakt Backup

Studiesteder

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ja

Beskrivelse

Inclusion Criteria:

  • written consent
  • Normal or corrected vision and hearing
  • Membership or entitlement to a social security plan
  • spoken and written French
  • third party liability insurance

for patients only :

  • at least 6 criteria for AUD based on the Diagnostic and statistical manual of mental disorders
  • At the end of withdrawal: treatment with a diazepam equivalent of ≤ 20 mg/day

Exclusion Criteria:

  • under tutorship/ judicial protection
  • Sensory or motor impairment (impeding the use of virtual reality and/or mobility)
  • Severe neurological disorder (such as dementia or Korsakoff's syndrome)
  • Photosensitive epilepsy (contraindication for the use of virtual reality)
  • Any other condition deemed incompatible with the study, at the investigator's discretion
  • Montreal Cognitive Assessment (MoCA) score < 10 (severe cognitive impairment)
  • Breastfeeding or pregnant women
  • Familiarity with the supermarket visited during the MET test

For controls only :

  • History of alcohol use disorder
  • score ≥ 8 on the Alcohol Use Disorders Identification Test
  • Score on the Frontal Assessment Battery < 16 (or < 15 if education is below secondary level)

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Andet
  • Tildeling: Ikke-randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: AUD group with executive function deficit
Group of patients with alcohol use disorder and a deficit in executive functions as assessed by the Frontal Assessment Battery
The test takes place in a real supermarket. Participants must complete a list of tasks (e.g., purchasing certain items, collecting some information) while adhering to rules (e.g., not visiting the same place twice, etc).

The test takes place in a virtual supermarket, developed on the C2Neuro app by C2CARE®.

Participants must complete a similar list of tasks to the MET (e.g., purchasing certain items, collecting some information) and adhere to similar to rules (e.g., not visiting the same place twice, etc) .

Aktiv komparator: AUD group without executive function deficit
Group of patients with alcohol use disorder but without a deficit in executive functions as assessed by the Frontal Assessment Battery
The test takes place in a real supermarket. Participants must complete a list of tasks (e.g., purchasing certain items, collecting some information) while adhering to rules (e.g., not visiting the same place twice, etc).

The test takes place in a virtual supermarket, developed on the C2Neuro app by C2CARE®.

Participants must complete a similar list of tasks to the MET (e.g., purchasing certain items, collecting some information) and adhere to similar to rules (e.g., not visiting the same place twice, etc) .

Aktiv komparator: Control group
Group of healthy volunteers
The test takes place in a real supermarket. Participants must complete a list of tasks (e.g., purchasing certain items, collecting some information) while adhering to rules (e.g., not visiting the same place twice, etc).

The test takes place in a virtual supermarket, developed on the C2Neuro app by C2CARE®.

Participants must complete a similar list of tasks to the MET (e.g., purchasing certain items, collecting some information) and adhere to similar to rules (e.g., not visiting the same place twice, etc) .

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Total number of errors on the test
Tidsramme: Baseline

Total number of errors on the MET and the V-MET.

Errors include:

  • Inefficiencies (a more effective action could have been made)
  • Rule breaks: a specific rule is broken
  • Interpretation failure (the task is misunderstood or misinterpreted)
  • Task failure: not carried out or not completely completed
Baseline

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Inefficiencies on the test
Tidsramme: Baseline
Inefficiencies on the MET/V-MET : a more effective action could have been made Can be infinite
Baseline
Rule breaks on the test
Tidsramme: Baseline
Rule breaks on the MET / V-MET : a specific rule is broken
Baseline
Task failures on the test
Tidsramme: Baseline
Task failures on the MET / V-MET : task not carried out or not completely completed
Baseline
Interpretation failures on the test
Tidsramme: Baseline
Interpretation failures on the MET/V-MET : the task is misunderstood or misinterpreted
Baseline

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Ledende efterforsker: Christophe ICARD, MD, CH le Vinatier

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

1. maj 2026

Primær færdiggørelse (Anslået)

1. juni 2028

Studieafslutning (Anslået)

1. juni 2028

Datoer for studieregistrering

Først indsendt

12. maj 2026

Først indsendt, der opfyldte QC-kriterier

12. maj 2026

Først opslået (Faktiske)

18. maj 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

20. maj 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

18. maj 2026

Sidst verificeret

1. maj 2026

Mere information

Begreber relateret til denne undersøgelse

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

JA

IPD-planbeskrivelse

Individual participant data (IPD) underlying the results reported in this study might be shared, including de-identified demographic data, baseline characteristics, outcome measures, and variables necessary to reproduce the analyses. All data will be fully anonymized to protect participant confidentiality. A data dictionary and relevant metadata might also be provided to facilitate interpretation and reuse.

The analytic code will be provided at the time of publication of the primary study results. De-identified IPD will be shared via an open science repository such as Open Science Framework and may also be made available upon request.

IPD-delingstidsramme

Data and supporting documents will be available beginning at the time of publication of the primary results

IPD-delingsadgangskriterier

Data will be made openly available

IPD-deling Understøttende informationstype

  • ANALYTIC_CODE

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