Research protocol of the efficacy of probiotics for the treatment of alcohol use disorder among adult males: A comparison with placebo and acceptance and commitment therapy in a randomized controlled trial

PLoS One. 2023 Dec 5;18(12):e0294768. doi: 10.1371/journal.pone.0294768. eCollection 2023.

Abstract

Background and aim: Primarily, this study compares the efficacy of probiotic and acceptance and commitment therapy (ACT) in alleviating the severity of alcohol craving and alcohol use disorder (AUD) among patients who had undergo two weeks of in-patient detoxification. Secondarily, this study compares the efficacy of probiotic and ACT in mitigating the severity of comorbid depression and anxiety symptoms; decreasing serum level of pro-inflammatory cytokines, such as interleukin 1β (IL-1β), interleukin 6 (IL-6), and tumor necrosis factor α (TNF-α); changing the event-related potential in electroencephalogram (EEG) and restoring microbiota flora in the gut of AUD patients.

Methods and analysis: Initially, during Phase I of the study, the serum level of IL-1β, IL-6 and TNF-α; ERP changes in the EEG and fecal microbiota content will be compared between 120 AUD patients and 120 healthy controls. Subsequently in Phase II of the study, 120 AUD patients will be randomized by stratified permuted block randomization into the probiotic, ACT and placebo groups in a 1:1:1 ratio. Participants in the probiotic and placebo groups will be administered one sachet per day of Lactobacillus spp. probiotic and placebo, respectively for 12 weeks. While those in the ACT group will receive one session per week of ACT for 8 weeks. Outcome measures will be administered at four timepoints, such as t0 = baseline assessment prior to intervention, t1 = 8 weeks after intervention began, t2 = 12 weeks after intervention and t3 = 24 weeks after intervention. Primary outcomes are the degrees of alcohol craving, alcohol withdrawal during abstinence and AUD. Secondary outcomes to be assessed are the severity of co-morbid depression and anxiety symptoms; the serum levels of IL-1β, IL-6 and TNF-α; changes in ERP and fecal microbiota content.

Trial registration number: NCT05830708 (ClinicalTrials.gov). Registered on April 25, 2023.

Publication types

  • Clinical Trial Protocol

MeSH terms

  • Acceptance and Commitment Therapy*
  • Adult
  • Alcoholism* / therapy
  • Clinical Trials, Phase II as Topic
  • Double-Blind Method
  • Humans
  • Interleukin-6
  • Male
  • Probiotics* / therapeutic use
  • Randomized Controlled Trials as Topic
  • Substance Withdrawal Syndrome*
  • Treatment Outcome
  • Tumor Necrosis Factor-alpha

Substances

  • Interleukin-6
  • Tumor Necrosis Factor-alpha

Associated data

  • ClinicalTrials.gov/NCT05830708

Grants and funding

This study is funded by the Open Project of Psychiatry and Neuroscience Discipline of Second Affiliated Hospital, Xinxiang Medical University (grant Number: 2022-xyefykfkt-003). The research fund was obtained by BZ. URL: https://www.xxmu.edu.cn/gjjlc/info/1051/1208.htm The funder did not and will not have a role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.