The Effectiveness of a Smartphone Application in the Treatment of Alcohol Use Disorder

Sponsor
St Patrick's Hospital, Ireland (Other)
Overall Status
Unknown status
CT.gov ID
NCT03396887
Collaborator
(none)
50
1
2
17
2.9

Study Details

Study Description

Brief Summary

Alcohol dependence poses a major problem for Irish and UK society, placing a huge burden on the health system. It is difficult to treat and relapse is common. There is an urgent need to develop novel treatment methods. One growing area of intervention is the use of mobile phone technology to develop personalised, patient-centred treatments. These can be used in outpatient settings, allowing patients to manage their own illness and take control of their recovery. In this study the investigators will investigate how a smartphone application, UControlDrink, can help alcoholics stay abstinent from alcohol. The application consists of a number of features known to aid recovery such as supportive messages and online therapy.

Condition or Disease Intervention/Treatment Phase
  • Other: U Control Drink Smartphone Application
  • Other: Control group
N/A

Detailed Description

Alcohol use disorder (AUD) is a common and difficult disorder to treat. Only a fraction of sufferers seek treatment and the rate of relapse is high. There is therefore an urgent need for improved methods of promoting long term abstinence and recovery in AUD. This study will explore the effectiveness of a smartphone application, UControlDrink, in aiding recovery from AUD in patients who have been discharged from an inpatient alcohol treatment programme. The application comprises five recovery focused features:

supportive messages, Computerised-Cognitive Behavioural Therapy, a drinking log, activities and trigger avoidance log, craving management and gamification. Patients will use the application for 3 months. A control group of patients will also be followed over the same time period. Cumulative abstinence duration as well as changes in questionnaire measures to baseline, time to first drink, proportion of patients continuously abstinent from alcohol, levels of activity within the app and patient satisfaction with their overall treatment will be measured at 3 months. If successful, this application may offer a unique, patient-centred, technology-driven, cost effective method of improving outcomes in AUD.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Participants will be randomised to intervention or control condition.Participants will be randomised to intervention or control condition.
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
The Effectiveness of a Smartphone Application in the Treatment of Alcohol Use Disorder
Actual Study Start Date :
May 1, 2017
Anticipated Primary Completion Date :
Jul 31, 2018
Anticipated Study Completion Date :
Sep 30, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: Smartphone Application Users

The experimental group will receive the smartphone intervention along with treatment as usual for 3-months. The smartphone application (UControlDrink) includes twice daily text message recovery support, relapse prevention cognitive behavioural therapy, 12 sessions in total, drinking and recovery activity logs where participants detail their abstinence, drinking and recovery activity engagement on a daily basis. Craving intervention in the form of a "calm button" to deal with cravings and prevent relapse and gamification, a system of encouraging positive behaviour with the awarding of "points" to achieve various "status" levels, is used to increase adherence and compliance with treatment recommendations.

Other: U Control Drink Smartphone Application
The smartphone application comprises five recovery focused features: supportive messages, Computerised-Cognitive Behavioural Therapy, a drinking log, craving management and gamification.

Active Comparator: Control Group

The control group will also receive treatment as usual, i.e. any follow-up after-care that they chose to participate in and regular AA/Lifering meetings.

Other: Control group
The control group will receive treatment as usual.

Outcome Measures

Primary Outcome Measures

  1. Number of drinking days [3 months]

    The number of drinking days will be assessed using the Time Line to Follow-Back scale (TLFB).The Alcohol TLFB is a descriptive questionnaire, using a calendar, participants will retrospectively record the number of days they drank over the previous 90 days. Drinking days will be calculated by summing the total number of days when alcohol was consumed in the previous 90 days.

  2. App activity score [3 months]

    Activity score on the app

  3. Units of alcohol consumed per drinking day [3 months]

    The Time Line Follow Back (TLFB) will be used to record the average number of units of alcohol consumed on drinking days.

Secondary Outcome Measures

  1. Time to first drink [3 months]

    Number of days to first drink

  2. Changes in the Alcohol Use Disorders Identification Test scores from baseline [3 months]

    Changes in scores on the Alcohol Use Disorders Identification Test between baseline and 3 month follow-up assessment.

  3. Changes in the Alcohol Abstinence Self-Efficacy Scale scores from baseline [3 months]

    Changes in the Alcohol Abstinence Self-Efficacy Scale scores between baseline and 3 month follow-up assessment.

  4. Changes in the Obsessive Compulsive Drinking Scale scores from baseline [3 months]

    Changes in scores on the Obsessive Compulsive Drinking Scale between baseline and 3 month follow-up assessment.

  5. Changes in the Beck Depression Inventory scores from baseline [3 months]

    Changes in scores on the Beck Depression Inventory between baseline and 3 month follow-up assessment.

  6. Changes in the Beck Anxiety Inventory scores from baseline [3 months]

    Changes in scores on the Beck Anxiety Inventory between baseline and 3 month follow-up assessment.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Patients will fulfil the criteria for an alcohol use disorder according to the Structured Clinical Interview for DSM-5 Axis I Disorders

  2. Patients must complete an alcohol treatment programme at St. Patrick's University Hospital.

  3. Primary addiction must be alcohol in poly-substance abusers.

  4. Aged over 18 years of age and capable of providing written, informed consent.

  5. Mini Mental State Examination (MSSE) score of ≥25.

  6. Patients must have an iphone or Android smartphone and are familiar with using smartphone applications.

Exclusion Criteria:
  1. Patients whose primary substance of abuse is not alcohol, although may meet the criteria for alcohol dependency/abuse.

  2. Patients who do not have an iPhone or Android smartphone.

  3. Age <18years or >70years.

  4. Psychotic disorder

  5. Patients who do not fully complete an inpatient treatment programme before discharge.

  6. History of alcohol use disorder but not current.

Contacts and Locations

Locations

Site City State Country Postal Code
1 St. Patrick's University Hospital Dublin Ireland Dublin 8

Sponsors and Collaborators

  • St Patrick's Hospital, Ireland

Investigators

  • Principal Investigator: Conor Farren, PhD,MRCPsych, St. Patrick's University Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Dr. Conor Farren, Consultant Psychiatrist, St Patrick's Hospital, Ireland
ClinicalTrials.gov Identifier:
NCT03396887
Other Study ID Numbers:
  • UCD - Protocol 19/15
First Posted:
Jan 11, 2018
Last Update Posted:
Jan 11, 2018
Last Verified:
Nov 1, 2017
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Dr. Conor Farren, Consultant Psychiatrist, St Patrick's Hospital, Ireland
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 11, 2018