MedPath

Virtual reality as a treatment for alcohol use disorder

Phase 2
Conditions
Middelgerelateerde en verslavingsstoornissen
alcohol addiction
Alcohol use disorder
Registration Number
NL-OMON51954
Lead Sponsor
Parnassia (Den Haag)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Not specified
Target Recruitment
10
Inclusion Criteria

Alcohol use disorder

Exclusion Criteria

Severe interfering psychiatric disorders (acute mood disorders, acute psychotic
disorders and neuropsychiatric disorders).

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>The main parameter is subjective craving. Subjective craving will be measured<br /><br>with questionnaires and participants will be asked to fill in the ASI, Mate<br /><br>CRIMI: verlangen and VAS before each treatment session. After the treatment<br /><br>session participants will be asked to fill in the VAS again. Three months after<br /><br>the last session participants will be asked to answer all the questionnaires<br /><br>mentioned above once more.</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>Secondary parameter will be physiological craving and self-efficacy, measured<br /><br>by self-report. The non-invasive physiological measures are heart rate<br /><br>variability and skin conductance, which will be measured with the Biopac<br /><br>software. Third, after each virtual reality session, participants will be asked<br /><br>to fill in the therapy evaluation scale to investigate how participants<br /><br>experienced the virtual reality cue exposure therapy. Also, alcohol relapse<br /><br>will be monitored through self-report and routine urine drug monitoring.</p><br>
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