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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06308484
Other study ID # TRR265 C02 FP2
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 20, 2024
Est. completion date June 30, 2027

Study information

Verified date March 2024
Source Charite University, Berlin, Germany
Contact Annika Rosenthal
Phone 030 450 517040
Email annika.rosenthal@charite.de
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Our primary objective is to integrate tVNS and mindfulness meditation within a structured mindfulness-based relapse prevention (MBRP) program for detoxified alcohol-dependent patients (AD). We aim to determine whether neuromodulation can enhance mindfulness-based relapse prevention compared to mindfulness practice alone. In this context, we will investigate potential changes in the interaction of top-down control and cue reactivity, as well as assess the severity of AUD. Measurements of drinking behavior, cravings, and abstinence rates will be conducted up to three months post-treatment. Our second objective is to examine the causal role of frontal midline theta oscillations (FMΘ) in MBRP and cognitive control. To achieve this, we will first establish closed-loop amplitude-modulated transcranial alternating current stimulation (CLAM-tACS) to selectively modulate FMΘ oscillations during MBRP meditation exercises in AUD patients (2).


Recruitment information / eligibility

Status Recruiting
Enrollment 140
Est. completion date June 30, 2027
Est. primary completion date June 30, 2027
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Alcohol Dependence (ICD-10) - abstinence between 3 days and 12 months Exclusion Criteria: - current (last 12 months) substance use disorder/dependence - neurological disorders (e.g. epilepsy, neuropathy, multiple sclerosis) - current severe major depressive disorder, manic episode or schizophreniform disorder - intake of anticonvulsive or high-potency antipsychotic medication

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Transcutaneous vagus nerve stimulation
Patients that are enrolled in a MBRP program will be subjected to weekly tVNS stimulation during a 30-minute audio guided mindfulness exercise.
Closed-loop AM-tACS
Patients that are enrolled in a MBRP program will be subjected to weekly CLAM-tACS stimulation during a 30-minute audio guided mindfulness exercise.

Locations

Country Name City State
Germany Charité - Berlin University of Medicine Berlin

Sponsors (2)

Lead Sponsor Collaborator
Charite University, Berlin, Germany Medical School Berlin

Country where clinical trial is conducted

Germany, 

References & Publications (3)

Ekhtiari H, Zare-Bidoky M, Sangchooli A, Janes AC, Kaufman MJ, Oliver JA, Prisciandaro JJ, Wustenberg T, Anton RF, Bach P, Baldacchino A, Beck A, Bjork JM, Brewer J, Childress AR, Claus ED, Courtney KE, Ebrahimi M, Filbey FM, Ghahremani DG, Azbari PG, Goldstein RZ, Goudriaan AE, Grodin EN, Hamilton JP, Hanlon CA, Hassani-Abharian P, Heinz A, Joseph JE, Kiefer F, Zonoozi AK, Kober H, Kuplicki R, Li Q, London ED, McClernon J, Noori HR, Owens MM, Paulus MP, Perini I, Potenza M, Potvin S, Ray L, Schacht JP, Seo D, Sinha R, Smolka MN, Spanagel R, Steele VR, Stein EA, Steins-Loeber S, Tapert SF, Verdejo-Garcia A, Vollstadt-Klein S, Wetherill RR, Wilson SJ, Witkiewitz K, Yuan K, Zhang X, Zilverstand A. A methodological checklist for fMRI drug cue reactivity studies: development and expert consensus. Nat Protoc. 2022 Mar;17(3):567-595. doi: 10.1038/s41596-021-00649-4. Epub 2022 Feb 4. — View Citation

Kleckner IR, Wormwood JB, Simmons WK, Barrett LF, Quigley KS. Methodological recommendations for a heartbeat detection-based measure of interoceptive sensitivity. Psychophysiology. 2015 Nov;52(11):1432-40. doi: 10.1111/psyp.12503. Epub 2015 Aug 12. — View Citation

Swick D, Ashley V, Turken U. Are the neural correlates of stopping and not going identical? Quantitative meta-analysis of two response inhibition tasks. Neuroimage. 2011 Jun 1;56(3):1655-65. doi: 10.1016/j.neuroimage.2011.02.070. Epub 2011 Mar 3. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Cognitive Control Before and after the treatment, we will assess cognitive control on a behavioral (response inhibition) and neurophysiological level (electroencephalogram) using a Simon GoNogo task, which reliably triggers activation of the frontal midline regions (Swick et al., 2011). Pre and post intervention after 6-8 weeks
Primary Interoception Additionally, interoceptive control is intended to be measured using a heartbeat detection task (Kleckner et al., 2015). Pre and post intervention after 6-8 weeks
Primary Cue-Reactivity Evaluate physiological reactivity to alcohol cues through a passive viewing task developed based on the guidelines of Ekhitiari et al. (2022) and measure subjective cue-induced cravings. Pre and post intervention after 6-8 weeks
Secondary Heartrate Heartrate change due to stimulation pre, ad interim at every tVNS and CLAM-tACS stimulation (once per week for 6-8 weeks), post after 6-8 weeks
Secondary Heartrate Variability Heartrate variability change due to stimulation pre, ad interim at every tVNS and CLAM-tACS stimulation (once per week for 6-8 weeks), post after 6-8 weeks
Secondary Mindfulness Trait and state mindfulness pre, post after 6-8 weeks
Secondary Alcohol consumption Frequency of drinking days and quantity of alcohol consumed pre, post after 6-8 weeks, follow-up three months later
Secondary Dependence Severity (Alcohol Dependence Scale) Craving, urge and dependence severity assessed via questionnaires. pre, post after 6-8 weeks, follow-up three months later
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