Alcohol Misuse Clinical Trial
Official title:
Internet-delivered Cognitive Behaviour Therapy for Alcohol Misuse: A Factorial Trial Examining the Effects of Assessment Interview and Guidance
NCT number | NCT03984786 |
Other study ID # | 2019-058 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | July 31, 2019 |
Est. completion date | April 11, 2024 |
Verified date | May 2024 |
Source | University of Regina |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Internet-delivered cognitive behaviour therapy (ICBT) shows considerable promise as a convenient treatment for alcohol misuse. ICBT may differ in whether the user works alone (self-guided) or along with an individual who guides treatment (e.g., therapist/health educator). Guided ICBT involves completing online lessons over several weeks coupled with support from a guide in the form of emails, online messages and/or brief telephone calls. Self-guided ICBT allows users to complete lessons by themselves without any contact with a guide. In some studies, guided-ICBT has shown greater reductions in alcohol consumption than self-guided ICBT. Further, some research on alcohol treatment shows that assessment in itself may have an effect on alcohol consumption, a phenomenon referred to in the literature as "assessment reactivity". It is believed that verbalizing one's drinking problems to another person might lead to greater realization of the problem extent and severity, which in turn can lead to initiation of the change process. Experimental studies have shown that extended and frequent assessments lead to greater alcohol reductions compared to brief and infrequent assessments. Although ICBT for alcohol misuse is an attractive treatment option, it is not often available to clients as part of routine care. The Online Therapy Unit at the University of Regina is currently exploring extending services to include guided ICBT for alcohol misuse. The Unit has been providing treatment in ICBT for depression and anxiety as well as various health conditions since 2010 and has offered treatment to ~4200 individuals. The purpose of this study is to evaluate ICBT for individuals with alcohol misuse within the routine online clinic, and to investigate ways to optimize future modes of delivery. Of specific interest in this study, is how outcomes vary depending on whether or not weekly guidance from a health educator is available and whether or not an initial extended assessment telephone call is included or not compared to a briefer screening telephone call. Of interest will also be if the extended assessment leads to greater alcohol reductions and higher motivation pre-treatment.
Status | Completed |
Enrollment | 312 |
Est. completion date | April 11, 2024 |
Est. primary completion date | January 5, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Timeline Followback (TLFB; preceding week alcohol consumption) > 13 drinks - Alcohol Use Disorders Identification Test (AUDIT) > 7 Exclusion Criteria: - Severe depression (measured by scoring > 23 on PHQ-9) - Suicidal ideation (measured by scoring > 2 to question 9 of PHQ-9) - Severe mental health or medical conditions - Severe drug use problems (measured by scoring > 24 on Drug Use Disorders Identification Test [DUDIT] or clinical assessment) - Low motivation to do, or concerns regarding, online treatment - Ongoing or impending significant mental health treatment - Not residing in Canada for the duration of treatment - Lack of or inconsistent access to a computer and internet at home or private place for the duration of treatment |
Country | Name | City | State |
---|---|---|---|
Canada | University of Regina | Regina | Saskatchewan |
Lead Sponsor | Collaborator |
---|---|
University of Regina | Ministry of Health, Saskatchewan, Saskatchewan Centre for Patient-Oriented Research, Saskatchewan Health Research Foundation |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Drinks preceding week as measured by Timeline Followback (TLFB) | Change in preceding week alcohol consumption in terms of the total number of standard drinks consumed on each day during the previous 7 days. | Screening, Pre-treatment, 4 weeks (mid-treatment), 8 weeks (post-treatment), 3 months after treatment, 6 months after treatment, 12 months after treatment | |
Primary | Heavy drinking days preceding week as measured by Timeline Followback (TLFB). | Change in preceding week alcohol consumption in terms of the total number of heavy drinking days during the previous 7 days. | Screening, Pre-treatment, 4 weeks (mid-treatment), 8 weeks (post-treatment), 3 months after treatment, 6 months after treatment, 12 months after treatment | |
Secondary | Alcohol Use Disorders Identification Test (AUDIT). | Change in alcohol-related problems and behaviours measured by total AUDIT score which can range from 0 to 40. Greater score indicates greater alcohol problems (worse outcome) | Screening, 8 weeks (post-treatment), 3 months after treatment, 6 months after treatment, 12 months after treatment | |
Secondary | Penn Alcohol Craving Scale | Change in alcohol craving as measured by a total score ranging between 0 to 30. Higher scores indicate greater craving (worse outcome). | Screening, 8 weeks (post-treatment), 3 months after treatment, 6 months after treatment, 12 months after treatment | |
Secondary | Brief Situational Confidence Questionnaire (BSCQ). | Change in confidence in resisting drinking urges in 8 situations rated from 0 to 100, rendering a sum score of 0-800. Higher scores indicate greater confidence (better outcome). There are 8 subscales, one for each item, assessed on a scale of 0-100. Thus, each subscale has a sum score of 0-100-. A higher score indicates greater confidence on the subscale. | Screening, 8 weeks (post-treatment), 3 months after treatment, 6 months after treatment, 12 months after treatment | |
Secondary | Generalized Anxiety Disorder 7-item (GAD-7) | Change in total GAD-7 anxiety score which can range from 0 to 21. Higher scores indicate greater anxiety (worse outcome) | Screening, 8 weeks (post-treatment), 3 months after treatment, 6 months after treatment, 12 months after treatment | |
Secondary | Patient Health Questionnaire (PHQ-9) | Change in total PHQ-9 score which can range from 0 to 27. Higher scores indicate greater depression (worse outcome) | Screening (Pre-treatment), 4 weeks (mid-treatment), 8 weeks (post-treatment), 3 months after treatment, 6 months after treatment, 12 months after treatment | |
Secondary | Sheehan Disability Scale | Change in three scores assessing functional impairment in three domains: 1) work/school, 2) social and 3) family life (each domain score ranges from 0 to 10, rendering a sum score of 0-30). Higher score indicates greater ability on the specified domain score (better outcome). Each domain score (subscale) renders a sum score of 0-10. | Screening, 8 weeks (post-treatment), 3 months after treatment, 6 months after treatment, 12 months after treatment | |
Secondary | Treatment Credibility and Expectancy Scale | Measures the participant's thoughts and feelings about the treatment and the treatment's effectiveness in reducing participant's symptoms and increasing participant's functioning. Consists of 6 items. The first three of these and the 5th render a score of 1- 9. The other three questions render a score of 0-10. There are two subscales; 1) treatment credibility and 2) treatment expectancy. The first three questions are summed to render a score on the credibility subscale (0-27). The last three questions, the expectancy subscale, render a score of 0-29. | 4 weeks (mid-treatment) | |
Secondary | Readiness to Change Questionnaire Treatment Version (RCQ-TV) | Measures participants' motivation to change their drinking behaviours and determines at which stage of the Stages of Change model they are in (precontemplation, contemplation, or action). There is no sum score. Instead the items related to each stage are summed, and the individual is allocated to the stage that has the greatest score out of these three. (For more information about the scoring of this instrument, see Heather & Hönekopp, 2009). | Screening (Pre-treatment) | |
Secondary | Evaluation and Negative Effects Questionnaire | Measures negative effects experienced by participants during treatment. This questionnaire has been developed by the research team, and does not have a sum score. | 8 weeks (post-treatment) |
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