Alcohol Abuse Clinical Trial
— SINCOfficial title:
Pilot Study on Mindfulness Meditation and Behavioral Flexibility Among Emerging Adults
Verified date | April 2024 |
Source | University of North Carolina, Chapel Hill |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Lifetime risk for developing an alcohol use disorder increases with earlier onset of alcohol consumption. This risk may reflect a tendency for escalated alcohol intake among youth due to immature executive control, leading to more frequent binge drinking, which is associated with more alcohol-related problems. Binge drinking is associated with deficits in behavioral flexibility, which may suggest impaired control networks that contribute to automatic behavior. Individuals with an alcohol or substance use disorder (A/SUD) exhibit attentional bias toward drug- or alcohol-related stimuli that have attained salience through consistent use. Reward history increases attention towards non-drug stimuli, even among individuals with no lifetime A/SUD. Preliminary data (from Dr. Boettiger's lab) from a nationally representative US adult sample using data collected via Prolific found that a questionnaire measure of mindfulness moderates the relationship between alcohol misuse and attention to reward. Given evidence that heavy alcohol drinking impairs behavioral flexibility, which in turn promotes escalating intake, insight into the relationship between mindfulness and behavioral flexibility could inspire new strategies to prevent alcohol and substance use disorders in people at elevated risk.
Status | Completed |
Enrollment | 16 |
Est. completion date | December 20, 2023 |
Est. primary completion date | December 20, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 19 Years |
Eligibility | Inclusion Criteria: - High school educated; college enrolled first-year student - Medically healthy - Ages 18-19 - Native-English speaker (or fluent < 7 years old) - Self-report of >4 lifetime binge drinking episodes (>4 drinks/2hours for females, >5 drinks/2 hours for males). Exclusion Criteria: - Psychiatric disease (such as depression or psychosis) using the MINI [25] - Systemic disease such as cancer, cardiovascular or inflammatory disease which could influence cognitive functioning - Motor or visual disturbance (e.g., colorblind) - Current use of psychoactive drugs (aside from moderate caffeine or alcohol), including prescription medications, or individuals with a known history of any substance use disorders (not including alcohol; including nicotine) or desire to seek treatment for excess substance (not including alcohol) use. |
Country | Name | City | State |
---|---|---|---|
United States | University of North Carolina at Chapel Hill | Chapel Hill | North Carolina |
Lead Sponsor | Collaborator |
---|---|
University of North Carolina, Chapel Hill | North Carolina Translational and Clinical Sciences Institute |
United States,
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* Note: There are 13 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Participant retention | Participant retention will be measured by the percentage of participants remaining in the study after 6 visits. | 10 weeks | |
Primary | Compliance with independent training of skills | To determine participant compliance with training skills learned during each of the 4 virtual visits, the total number of journal entries logged during the 4 weeks of training is calculated as a total score. Total scores range from 0 to 24, with higher scores indicating greater compliance with independent training. | 6 weeks | |
Secondary | Expectancy of interventions | The Credibility/Expectancy Questionnaire (CEQ) is a 6-item questionnaire composed of two self-report scales that measure the the credibility and expectancy of an intervention in clinical studies. The word "therapy" is replaced with "intervention" and modified to reflect the intent of the intervention (i.e., to improve skills in navigating college). Four items are rated on a 1-9 Likert-type scale (0=not at all, to 9=very much), and two items are rated on a Likert-type percentage scale (0 to 100%). Credibility ratings are calculated by taking the mean of the first three items of the CEQ, and expectancy rating is calculated by taking the score from one question. | 1 week | |
Secondary | Emotional distress | The Depression, Anxiety and Stress Scale-21 (DASS-21) is composed of three self-report scales that measure depression, anxiety and stress. Items are rated on a Likert-type scale (0=Did not apply to me at all, to 3=Applied to me very much, or most of the time). Scores for the three subscales are calculated by summing the scores for the relevant items. The severity rating for Depression are Normal: 0-4, Mild: 5-6, Moderate: 7-10, Severe: 11-13, and Extremely Severe: 14-21; for Stress the ratings are Normal: 0-7, Mild: 8-9, Moderate: 10-12, Severe: 13-16, and Extremely Severe 17-21; and for Anxiety the ratings are Normal: 0-3, Mild: 4-5, Moderate: 6-7, Severe: 8-9, and Extremely Severe: 10-21. The total DASS-21 score is calculated by summing all three subscales, with a range from 0-63. For all scales, higher scores indicate greater emotional distress. | 10 weeks |
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