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

NCT ID: NCT03396887

Last Updated: 2018-01-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-05-01

Study Completion Date

2018-09-30

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Alcohol Use Disorder

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Participants will be randomised to intervention or control condition.
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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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.

Group Type EXPERIMENTAL

U Control Drink Smartphone Application

Intervention Type OTHER

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

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.

Group Type ACTIVE_COMPARATOR

Control group

Intervention Type OTHER

The control group will receive treatment as usual.

Interventions

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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.

Intervention Type OTHER

Control group

The control group will receive treatment as usual.

Intervention Type OTHER

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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St Patrick's Hospital, Ireland

OTHER

Sponsor Role lead

Responsible Party

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Dr. Conor Farren

Consultant Psychiatrist

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Conor Farren, PhD,MRCPsych

Role: PRINCIPAL_INVESTIGATOR

St. Patrick's University Hospital

Locations

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St. Patrick's University Hospital

Dublin, , Ireland

Site Status RECRUITING

Countries

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Ireland

Central Contacts

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Conor Farren, PhD,MRCPsych

Role: CONTACT

+35312493523

Facility Contacts

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Conor Farren, PhD MRCPsych

Role: primary

+35312493523

Other Identifiers

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UCD - Protocol 19/15

Identifier Type: -

Identifier Source: org_study_id

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