Optimisation of Functional MRI-based Neurofeedback for Alcohol Use Disorders
- Conditions
- Alcohol Abuse
- Interventions
- Other: Neurofeedback
- Registration Number
- NCT02406456
- Lead Sponsor
- Cardiff University
- Brief Summary
Participants will undergo a single session of functional magnetic resonance imaging (fMRI)-based neurofeedback (approximately 1 hour). The investigators will assess their ability to regulate motivational networks of the brain during the exposure to alcohol cues and evaluate immediate effects on craving and cognitive bias for alcohol by administering a questionnaire and a Stroop task before and after the session.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 15
- History of alcohol use disorder or current alcohol consumption above 21 units (1 unit = 8g) of alcohol per week (male participants) or above 14 units of alcohol per week (female participants)
- MRI safety exclusion criteria
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Neurofeedback Neurofeedback -
- Primary Outcome Measures
Name Time Method Neurofeedback success (brain activation difference during neurofeedback and baseline blocks) 1 day This measure will be based on the analysis of participants' fMRI (functional magnetic resonance imaging) data, reflecting brain activation, during exposure to alcohol cues. Neurofeedback success will be defined as significant difference between activation levels (expressed as beta weights of a linear regression model) during the regulation periods compared to baseline. The significance will be determined by a t-test.
- Secondary Outcome Measures
Name Time Method Alcohol Stroop task as a measure of cognitive bias 1 day Measure of cognitive bias
Drinking Urges Questionnaire as a measure of alcohol craving 1 day Measure of alcohol craving
Trial Locations
- Locations (1)
School of Medicine, Cardiff University
🇬🇧Cardiff, Wales, United Kingdom