Actively Recruiting
Towards Neurobehavioral Profiles and Models of Adaptive Stress Responses and Resilience in Individuals With Alcohol Use Disorder
Led by Central Institute of Mental Health, Mannheim · Updated on 2025-04-29
100
Participants Needed
2
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating how people with alcohol use disorder (AUD) respond to stress over time and what makes some stress responses adaptive or non-adaptive. The study aims to understand how stress, social interactions, coping strategies, and personal health behaviors affect alcohol craving and use. This observational study uses repeated stress exposure to explore brain and behavior patterns related to stress resilience and alcohol use. Participants will undergo an experimental setup twice on consecutive days that includes a rest period, a Trier Social Stress Test to induce social stress, exposure to their favorite alcoholic drink in a bar-like setting, and a functional MRI scan. The fMRI will assess brain activity related to alcohol cues, response inhibition, emotion processing, and resting state connectivity. After these visits, participants will enter a six-week ambulatory phase where they report daily on stressors, alcohol craving, consumption, social interactions, and health behaviors using smartphone tools. During the study, researchers will measure cortisol levels, alcohol urges and craving, subjective stress, and brain responses at multiple times each day of testing. Blood pressure will also be monitored. The daily assessments during the ambulatory phase will help determine how stress responses observed in the lab relate to real-life experiences of stress and alcohol use. The study participation includes eligibility screening, two experimental visits, and six weeks of daily monitoring, with careful evaluation of stress and alcohol-related behaviors.
CONDITIONS
Brief Title
Neurobehavioral Profiles of Adaptive Stress Responses in Individuals With Alcohol Use Disorder
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 16 and 65 years
- Meet at least 2 criteria of alcohol use disorder according to DSM-5 without current need for therapeutic intervention
- Fluent in German
- Able to understand study procedures and give informed consent
- Willingness to use a study smartphone
You will not qualify if you...
- Current use of drugs or medications that interact with the central nervous system or glucocorticoid system
- Contraindications for magnetic resonance imaging
- History of bipolar disorder, psychotic disorder, schizophrenia or related disorders, or substance use disorder other than alcohol, nicotine, or cannabis
- History of severe head injury, severe central nervous system disorders, or severe somatic disorders such as liver cirrhosis
- Pregnancy
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 telephone screening visit
Duration - 2 days
Participants undergo two experimental study visits on consecutive days involving a rest period, stress test, alcohol cue exposure, and brain imaging to assess stress responses and neural activity.
2 in-person visits on consecutive days
Duration - 6 weeks
Participants complete daily smartphone-based assessments over six weeks to track stress exposure, alcohol craving and use, and health behaviors in everyday life.
Daily remote assessments via smartphone
Trial Site Locations
Total: 2 locations
1
Central Institute of Mental Health
Mannheim, Baden-Wurttemberg, Germany, 68159
Actively Recruiting
2
Central Institute of Mental Health
Mannheim, Germany, 68159
Actively Recruiting
Research Team
P
Patrick Bach, MD, PhD
J
Judith Zaiser
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1