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Alcohol Use Disorder (AUD)EVIMETALNCT07593664

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

A study testing Multiple Errand Test (MET) and Virtual MET in people with Alcohol Use Disorder (AUD), run by Hôpital le Vinatier at 2 sites in France.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 to 65 yearsHealthy volunteers can take part
Conditions the study is for
Alcohol Use Disorder (AUD)
What is being tested?
Multiple Errand Test (MET) and Virtual MET
Could I receive a placebo?
No, everyone receives an active treatment
How many people
90 participants
Where
2 sitesFrance
Study dates
May 2026to Jun 2028
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • 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

Who cannot join

  • 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)
Show all 12Show fewer
  • 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)

Trial locations and contacts

2 sites in 1 country. Contact the study team or a site near you to ask about taking part.

France2 sites
  • CH Le Vinatier

    Bron, 69500

  • Hôpital de la Croix Rousse

    Lyon, 69004

    Louis-Ferdinand LESPINE, PhD, 0033437915514, Louis-ferdinand.LESPINE@ch-le-vinatier.fr

Other trials in France

About this study

Official title: 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:

Read more
  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.

Read the detailed description

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
Being tested
Multiple Errand Test (MET), Virtual MET
Keywords
Multiple Errands Test, Executive functions, Virtual reality, Alcohol Use Disorder
Medical subject headings
Alcoholism

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Multiple Errand Test (MET)Behavioural

    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).

  • Virtual METBehavioural

    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) .

Study groups in NCT07593664
Study groupRoleWhat they receive
AUD group with executive function deficitExperimentalGroup of patients with alcohol use disorder and a deficit in executive functions as assessed by the Frontal Assessment Battery
Receives: Behavioral: Multiple Errand Test (MET); Behavioral: Virtual MET
AUD group without executive function deficitActive comparatorGroup of patients with alcohol use disorder but without a deficit in executive functions as assessed by the Frontal Assessment Battery
Receives: Behavioral: Multiple Errand Test (MET); Behavioral: Virtual MET
Control groupActive comparatorGroup of healthy volunteers
Receives: Behavioral: Multiple Errand Test (MET); Behavioral: Virtual MET

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Total number of errors on the test

    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

    Measured: Baseline

Secondary outcomes (4)
  1. Inefficiencies on the test

    Inefficiencies on the MET/V-MET : a more effective action could have been made Can be infinite

    Measured: Baseline

  2. Rule breaks on the test

    Rule breaks on the MET / V-MET : a specific rule is broken

    Measured: Baseline

  3. Interpretation failures on the test

    Interpretation failures on the MET/V-MET : the task is misunderstood or misinterpreted

    Measured: Baseline

  4. Task failures on the test

    Task failures on the MET / V-MET : task not carried out or not completely completed

    Measured: Baseline

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 May 2026
  2. Study startMay 2026 (estimated)
  3. Primary completionJun 2028 (estimated)
  4. Study completionJun 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Non-randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
90 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07593664
Sponsor's protocol ID
2025-A00421-48
Acronym
EVIMETAL
Status last verified
May 2026
First submitted
12 May 2026
Last updated
20 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: 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.

Questions about this trial

What is this clinical trial studying?

A study testing Multiple Errand Test (MET) and Virtual MET in people with Alcohol Use Disorder (AUD), run by Hôpital le Vinatier at 2 sites in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 8 inclusion and 12 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 20 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Louis-Ferdinand LESPINE, PhD (+33437915155, Louis-ferdinand.LESPINE@ch-le-vinatier.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Total number of errors on the test (time frame: Baseline). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 May 2026; AzTrials last refreshed its copy on 26 Oct 2026.

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