MedPath

Sex Differences, Cognitive Training & Emotion Processing

Not Applicable
Completed
Conditions
Alcohol Use Disorder
Interventions
Other: Affective Training
Other: Neutral Training
Registration Number
NCT03137654
Lead Sponsor
University of Florida
Brief Summary

This pilot project addresses two understudied questions related to neurocognitive deficits observed in treatment-seeking alcoholics. First, whether cognitive training improves performance and outcomes in alcoholics, and whether men and women differ in their response to this training. The second is whether directed training using affective materials (e.g., emotional faces) is differentially effective compared to that using traditional (i.e., neutral) stimuli.

Detailed Description

This pilot project leverages the team's expertise in neurobehavioral assessment and focus on sex differences to examine the potential efficacy of cognitive training in treatment-seeking men and women with alcohol use disorders (AUDs). Specifically, the ask whether cognitive training interventions derived from current methods and conceptual models has differential benefits for treatment-seeking women vs. men. Although neurocognitive improvement during training is desired, of practical import is whether gains achieved transfer to other tasks and settings. Therefore, transfer of gains to tasks/domains varying in their similarity to training are assessed. Given noted sex differences in emotional processing and the purported role of emotional factors in women's substance use, training engaging emotional processing via the use of affective stimuli (faces and words) is included, predicting that women may differentially benefit from such training. Equal numbers of treatment-seeking men and women with AUDs will be randomly assigned to one of two active training interventions (neutral or affective stimuli). To control for abstinence-related recovery, a third group of participants, meeting identical selection criteria, will complete pre and post-intervention testing, but will not undergo the training intervention. Ss will complete baseline, 3 wks training (for active groups) and post-intervention testing and will be contacted monthly for 3 months after discharge.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
82
Inclusion Criteria
  • Minimum of 10 years of education
  • Subjects must have 20/40 or better corrected vision (determined by Snellen chart)
  • have no significant hearing impairment as determined by self-report and audiometric testing
  • must meet criteria for DSM-IV alcohol dependence using the computerized Diagnostic Interview Schedule - IV
  • A craving index is also administered to allow discussion in terms of DSM 5 classification.
  • Comorbid substance use including nicotine use is not exclusionary.
Read More
Exclusion Criteria
  • May not have medical or psychiatric histories which would confound participation or data interpretation, e.g., epilepsy, stroke, untreated hypertension, psychotic disorders, anxiolytic medications.
  • not be color blind (as determined by psuedoisochromatic plates)
  • Endorsement of suicidal intent
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Affective TrainingAffective TrainingSubjects complete baseline assessment, 3 wks of training with versions of the tasks using emotionally-laden stimuli, and a post-training assessment. Subjects will be contacted monthly for 3 months after discharge for follow-up interviews.
Neutral TrainingNeutral TrainingSubjects complete baseline assessment, 3 wks of training with versions of the tasks using neutral stimuli, and a post-training assessment. Subjects will be contacted monthly for 3 months after discharge for follow-up interviews.
Primary Outcome Measures
NameTimeMethod
Stroop Color-Word Task: Change from baseline in response timeBaseline and Post-Training (3 weeks)

An interference task involving target words (e.g., red) presented in interfering colors (e.g., blue). The primary dependent measure is change in reaction time from baseline to post-training assessment.

Emotional Stroop: Change from baseline in reaction timeBaseline and Post-Training (3 weeks)

An interference task involving target words presented over non-target visual stimuli. The primary dependent measure is change in reaction time on trials with incongruent stimuli (e.g., a negative word presented over a "happy" face) from baseline to post-training assessment.

Trail-Making Task A: Change from baseline in task completion timeBaseline and Post-Training (3 weeks)

A psychomotor and visual perception task wherein participants connect numbered dots by drawing a continuous line. The primary dependent measure is change in task completion time from baseline to post--training assessment.

Trail-Making Task B: Change from baseline in task completion timeBaseline and Post-Training (3 weeks)

A psychomotor and visual perception task with a set-shifting component wherein participants connect numbered and lettered dots by drawing a continuous line. The primary dependent measure is change in task completion time from baseline to post-training assessment.

Little Man Task: Change from baseline in response accuracy.Baseline and Post-Training (3 weeks)

A visual perception task involving mental rotation. The primary dependent measure is the change in response accuracy from baseline to post-training assessment.

Digit Symbol Substitution: Change from baseline in translated symbolsBaseline and Post-Training (3 weeks)

A psychomotor and set-shifting task involving translation between numbers and symbols. The primary dependent measure is the change in number of correctly translated symbols within 90 seconds from baseline to post-training assessment.

Wisconsin Card Sorting Task: Change from baseline in response accuracyBaseline and Post-Training (3 weeks)

A reasoning and set-shifting task. Participants must determine novel rule sets for stimuli matching through trial and error. Ss must match each 'Test Card' with a 'Key Card'. Criteria for a successful match shift throughout the testing session and may include color, shape, and number of symbols. The primary dependent measure is the change in response accuracy from baseline to post-training assessment.

Visual-Perceptual Analysis Task: Change from baseline in response accuracyBaseline and Post-Training (3 weeks)

A discrimination task in which participants are asked to determine which complex shape differs among a set of three.

Sternberg Working Memory Task: Change from baseline in response accuracyBaseline and Post-Training (3 weeks)

A working memory task involving numbers presented visually. Ss are presented with a list of digits, one at a time, followed by a probe digit. They must determine if the probe digit was in the original set of digits and recall the digits. The primary dependent measure is the change in response accuracy from baseline to post-training assessment.

Secondary Outcome Measures
NameTimeMethod
Profile of Mood StatesApproximately 30/60/90 days following post-training assessment

Mood/affect assessment in which participants indicate whether presented words describe how they have felt during the past week on a scale from 0-4, where 0 indicates "not at all"; 1 indicates "a little"; 2 indicates "moderately"; 3 indicates "quite a bit"; and 4 indicates "extremely".

Mini Alcohol Craving Experience questionnaireApproximately 30/60/90 days following post-training assessment

Indexes alcohol craving frequencies. Questions include:

1. Over the past week, how often did you have a strong urge to drink?

2. Over the past week, how often did you picture alcohol or drinking?

3. Over the past week, how often did you imagine what it would taste like?

4. Over the past week, how often did you imagine how your body would feel if you had a drink?

5. Over the past week, how often were these thoughts intrusive?

Participants respond on a scale from 1-10 for each question.

Timeline Follow-backApproximately 30/60/90 days following post-training assessment

Measures frequency and quantity of daily substance use.

Moos Health and Daily Living ScaleApproximately 30/60/90 days following post-training assessment

Measures social support and activities.

Trial Locations

Locations (5)

ASPIRE Healthcare Facilities

🇺🇸

Gainesville, Florida, United States

University of Florida

🇺🇸

Gainesville, Florida, United States

The Sid Martin Bridge House

🇺🇸

Gainesville, Florida, United States

UF Health Florida Recovery Center

🇺🇸

Gainesville, Florida, United States

Steward-Marchman-Act (SMA) Healthcare

🇺🇸

Multiple Locations, Florida, United States

© Copyright 2025. All Rights Reserved by MedPath