Sex Differences, Cognitive Training & Emotion Processing

Sponsor
University of Florida (Other)
Overall Status
Completed
CT.gov ID
NCT03137654
Collaborator
National Institute on Alcohol Abuse and Alcoholism (NIAAA) (NIH)
82
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3
41.8
16.4
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Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Affective Training
  • Other: Neutral Training
N/A

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
82 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
The primary design is a 3 (Training Condition: Neutral, Affective, Control) by 2 (Time: Baseline, Post-training) repeated measures design.The primary design is a 3 (Training Condition: Neutral, Affective, Control) by 2 (Time: Baseline, Post-training) repeated measures design.
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Sex Differences, Cognitive Training & Emotion Processing
Actual Study Start Date :
Aug 16, 2017
Actual Primary Completion Date :
Feb 8, 2021
Actual Study Completion Date :
Feb 8, 2021

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Affective Training

Subjects 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.

Other: Affective Training
Intervention includes up to 12 training sessions (~45 minutes each). Training sessions includes practice on cognitive tasks embedded with emotionally salient stimuli. Tasks include a dual modality n-back and a directed attend/ignore memory task.

Active Comparator: Neutral Training

Subjects 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.

Other: Neutral Training
Intervention includes up to 12 training sessions (~45 minutes each). Training sessions includes practice on cognitive tasks embedded with neutral stimuli. Tasks include a dual modality n-back and a directed attend/ignore memory task.

No Intervention: Control (Non-active)

Subjects complete a baseline assessment and a secondary assessment approximately three weeks later. No active intervention is delivered. Subjects will be contacted monthly for 3 months after discharge for follow-up interviews.

Outcome Measures

Primary Outcome Measures

  1. Emotional Stroop: Change from baseline in reaction time [Baseline 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.

  2. Trail-Making Task A: Change from baseline in task completion time [Baseline 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.

  3. Trail-Making Task B: Change from baseline in task completion time [Baseline 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.

  4. Digit Symbol Substitution: Change from baseline in translated symbols [Baseline 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.

  5. 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.

  6. Wisconsin Card Sorting Task: Change from baseline in response accuracy [Baseline 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.

  7. Sternberg Working Memory Task: Change from baseline in response accuracy [Baseline 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.

  8. Stroop Color-Word Task: Change from baseline in response time [Baseline 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.

  9. Visual-Perceptual Analysis Task: Change from baseline in response accuracy [Baseline and Post-Training (3 weeks)]

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

Secondary Outcome Measures

  1. Timeline Follow-back [Approximately 30/60/90 days following post-training assessment]

    Measures frequency and quantity of daily substance use.

  2. Moos Health and Daily Living Scale [Approximately 30/60/90 days following post-training assessment]

    Measures social support and activities.

  3. Profile of Mood States [Approximately 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".

  4. Mini Alcohol Craving Experience questionnaire [Approximately 30/60/90 days following post-training assessment]

    Indexes alcohol craving frequencies. Questions include: Over the past week, how often did you have a strong urge to drink? Over the past week, how often did you picture alcohol or drinking? Over the past week, how often did you imagine what it would taste like? Over the past week, how often did you imagine how your body would feel if you had a drink? Over the past week, how often were these thoughts intrusive? Participants respond on a scale from 1-10 for each question.

Eligibility Criteria

Criteria

Ages Eligible for Study:
25 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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.

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

Contacts and Locations

Locations

Site City State Country Postal Code
1 ASPIRE Healthcare Facilities Gainesville Florida United States 32607
2 The Sid Martin Bridge House Gainesville Florida United States 32608
3 UF Health Florida Recovery Center Gainesville Florida United States 32608
4 University of Florida Gainesville Florida United States 32611
5 Steward-Marchman-Act (SMA) Healthcare Multiple Locations Florida United States 32177

Sponsors and Collaborators

  • University of Florida
  • National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Investigators

  • Principal Investigator: Sara Jo Nixon, PhD, University of Florida
  • Principal Investigator: Ben Lewis, PhD, University of Florida

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Florida
ClinicalTrials.gov Identifier:
NCT03137654
Other Study ID Numbers:
  • IRB201700206-N
  • R03AA025430
First Posted:
May 3, 2017
Last Update Posted:
Apr 22, 2021
Last Verified:
Apr 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of Florida
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 22, 2021