Internet-based A-CRA for Young Adults With Problematic Alcohol Use

Overview

The primary aim of the study is to evaluate the feasibility and acceptability of an internet-delivered Adolescent Community Reinforcement Approach (I-A-CRA) with therapist support for young adults (aged 18-24 years) with problematic alcohol use and their caregiver/significant other. Secondary aims include investigating the role of comorbid emotional symptoms, emotion regulation and prosocial behavior in treatment outcomes for the young adults. In a randomized controlled pilot trial, participants (n = 60 young adults as well as an optional accompanying caregiver/significant other) will be recruited from the community through advertisements as well as through clinic referrals in Stockholm, Sweden. Eligible participants will be randomized either to the 10-week I-A-CRA treatment or to an active control group (receiving psychoeducation about alcohol use over the same time frame). In both conditions an optionally accompanying caregiver/significant other will receive a support program in conjunction with the young adult's treatment. Participating young adults will be evaluated with regards to their alcohol use, psychiatric symptoms, emotion regulation, and prosocial behavior at pre-treatment, weekly during treatment, post-treatment, and at a 3-month follow-up. The primary outcome will be feasibility (measured as number of treatment completers; i.e., having completed 5 out of 8 treatment modules), and acceptability (measured by patient satisfaction). Secondary outcomes will include pre- and post-treatment self-rated binge drinking episodes, levels of depression, anxiety and stress, emotion dysregulation, and prosocial behavior. Self-reports regarding stress, emotion dysregulation, and prosocial behavior will be complemented by behavioral measures (computerized tasks).

Full Title of Study: “Internet-based Adolescent Community Reinforcement Approach (I-A-CRA) With Therapist Support for Young Adults With Problematic Alcohol Use: A Randomized Controlled Trial”

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Randomized
    • Intervention Model: Parallel Assignment
    • Primary Purpose: Treatment
    • Masking: None (Open Label)
  • Study Primary Completion Date: September 2022

Interventions

  • Behavioral: Internet-delivered Adolescent Community Reinforcement Approach (I-A-CRA)
    • The intervention is a behavioral internet-based intervention based on the Adolescent Community Reinforcement Approach. The program encompasses text, pictures, videos, and written as well as practical assignments (skills training). The main components of the treatment for the young adult with problematic alcohol use consist of psychoeducation and functional analysis, goal formulation, increasing prosocial behaviors, relapse prevention, problem solving, and communication training. The accompanying significant other receives modules containing information focusing on gaining an understanding of the treatment components aimed at the young adult, as well as communication training to improve communication between the young adult and the significant other.
  • Behavioral: Psychoeducation, information on use of alcohol and its effects
    • The intervention is a behavioural internet-based intervention including psychoeducation focusing on providing information on alcohol, alcohol use, and its effects. The psychoeducation is provided via texts and pictures, and there is a possibility of asking questions to a therapist if needed however no therapist contact is mandatory. There are separate programs directed towards the young adult and the accompanying significant other. The programmes give brief self-help tips at the end. The intervention approximately corresponds to the information given in a primary care setting for someone with problematic alcohol use.

Arms, Groups and Cohorts

  • Experimental: I-A-CRA
    • Internet-delivered Adolescent Community Reinforcement Approach: The treatment program consists of 8 extensive treatment modules delivered over 10 weeks with continuous therapist support and guidance. There are two separate treatments for the young adult and the caregiver/significant other.
  • Active Comparator: Psychoeducation alcohol use
    • Psychoeducation focusing on alcohol use: This support program provides 8 brief modules of psychoeducation (alcohol information) over 10 weeks. Participants receive no therapist guidance/support but have the possibility of asking questions to a therapist. There are two separate programs for the young adult and the caregiver/significant other.

Clinical Trial Outcome Measures

Primary Measures

  • Percentage of treatment completers defined as patients completing 5 or more of the 8 modules of treatment
    • Time Frame: Will be assessed post treatment (11 weeks after treatment initiation)
    • Outcome used to assess feasibility.
  • Client Satisfaction Questionnaire 8 item
    • Time Frame: Will be assessed post treatment (11 weeks after treatment initiation)
    • Acceptance will be measured as percentage of participants rating their satisfaction as good. Higher score indicates better outcome. Scores range from 8-32.

Secondary Measures

  • Timeline Follow-back – change in time spent doing activities unrelated to drinking
    • Time Frame: Will be assessed before treatment initiation, at week 1, 2, 3, 4, 5, 6, 7, 8, 9 and 10 of treatment, and post treatment (11 weeks after treatment initiation)
    • Number of self-reported activities registered that are not related to alcohol consumption over the past week. More episodes is a better outcome.
  • Alcohol Use Disorders Identification Test – change pre to post treatment
    • Time Frame: Will be assessed before treatment initiation and post treatment (11 weeks after treatment initiation)
    • Self-reported screening of alcohol use disorder symptoms. Higher scores indicate worse outcome. Scores range from 0-40.
  • Difficulties in Emotion Regulation Scale 16 item – change over timepoints
    • Time Frame: Will be assessed before treatment initiation, at week 1, 2, 3, 4, 5, 6, 7, 8, 9 and 10 of treatment, and post treatment (11 weeks after treatment initiation)
    • Self-report scale measuring emotion dysregulation. Higher scores indicate worse outcome. Scores range from 16-80.
  • Depression Anxiety Stress Scale-21 – change pre to post treatment
    • Time Frame: Will be assessed before treatment initiation and post treatment (11 weeks after treatment initiation)
    • Self-report scale measuring symptoms of depression, anxiety and stress over the past week. Higher scores indicates worse outcome. Scores range from 0-42.
  • Timeline Follow-back – change in self-rated alcohol consumption
    • Time Frame: Will be assessed before treatment initiation, at week 1, 2, 3, 4, 5, 6, 7, 8, 9 and 10 of treatment, and post treatment (11 weeks after treatment initiation)
    • Number of heavy drinking episodes (heavy drinking defined as 4 or more drinks per drinking occasion in women and 5 or more for men) over the past week. Fewer episodes is a better outcome.

Participating in This Clinical Trial

Inclusion Criteria

  • Young adult between 18-24 years of age – Reporting ongoing substance use (alcohol), heavy drinking measured as risky use according to recommendations: 5/4 (male/female) standard drinks on a minimum of two occasions in the last month, or AUDIT-C ≥ 4 points indicating harmful consumption – Access to internet via computer or other similar device, as well as access to smartphone – If on psychiatric medication, it should have been a stable dosage during the past 3 months prior to pre-treatment assessment – Adequate knowledge in the Swedish language and a Swedish personal identification number Exclusion Criteria:

  • Current DSM-5 diagnosis for any other substance use disorder except nicotine dependence – Current (including last 12 months) DSM-5 diagnosis for other major psychiatric disorder (bipolar disorder, psychosis) – Recent initiation of psychiatric medication or psychotherapy (within the last 3 months) – Suicidal ideation at screening – Serious somatic diagnosis requiring medical attention, such as uncontrolled diabetes mellitus, epilepsy or heart conditions – Traces of any psychoactive substance (e.g., central stimulant amines, THC, benzodiazepines, opiates, cocaine) in urine sample at baseline assessment – Pregnancy

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: 24 Years

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • Nitya Jayaram-Lindstrom
  • Provider of Information About this Clinical Study
    • Sponsor-Investigator: Nitya Jayaram-Lindstrom, Principal Investigator – Karolinska Institutet
  • Overall Official(s)
    • Nitya Jayaram-Lindstrom, Ph.D., Principal Investigator, Department of Clinical Neuroscience, Karolinska Institutet
  • Overall Contact(s)
    • Maria E AAbonde Garke, M.Sc., 70 285 96 14, maria.garke@ki.se

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