New Relapse Model in Psychiatry
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Auto-questionnaires, hetero-questionnaires and Evoked-potentials.
- Who it may be relevant to
- Registry conditions: Alcohol Use Disorder. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Belgium
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Creation of a Visualization Tool With Integrated Clinical Data to Support Clinical Intervention and Empowerment of Inpatients in Psychiatry : Basis for the Development of a Predictive Model of Relapse
Overview
The goal of this clinical trial is to learn about risk factors of relapse in patients with alcohol use disorder. The main questions it aims to answer are : * Among patients with Alcohol Use Disorder, are there clusters of patients with the same characteristics and the same outcome ? * Which are the risk factors of relapse that are the most predictive ? Do they vary according to cluster? * Can a feedback-measurment-system (eg : a feedback of the tests' results) be usefull in a detoxification unit ? Participants will : * Complete auto-questionnaires * Pass hetero-evaluations * Undergo an electrophysiological battery
Interventions
- Other Auto-questionnaires, hetero-questionnaires and Evoked-potentials
Evaluations of risk factors of relapse by questionnaires, evaluation of evoked-potentials
Primary outcome measures
- Relapse or abstinence after detoxification [Time frame: Throughout the entire study, approximately during 48 months]
Secondary outcome measures (1)
- Satisfaction of the feedback-measurment-system for clinicians and patients [Time frame: Throughout the entire study, approximately during 48 months]
Eligibility criteria
Inclusion criteria
- To suffer from AUD
- To be hospitalized
- To speak French fluently
- To be able to give their consent (medically and legally).
Exclusion criteria
- To suffer from severe perceptive disabilities (auditory, visual)
- To suffer from severe cognitive impairment
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Other
Study locations
Belgium · 1 center
- Cliniques Universitaires Saint-Luc — Brussels
Identifiers
NCT: NCT06244641 · 2023/09MAI/22