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Computerized Cognitive Training in Middle-Aged Adults With Generalized Anxiety Disorder: A Pilot Study

Computerized Cognitive Training in Middle-Aged Adults With Generalized Anxiety Disorder: A Pilot Study (COGMA)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04421690
Acronym
COGMA
Enrollment
30
Registered
2020-06-09
Start date
2020-06-08
Completion date
2022-06-30
Last updated
2023-03-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Generalized Anxiety Disorder

Keywords

Anxiety, Middle-Aged, Sleep, Cognition, Older Adults

Brief summary

The purpose of this research is to look at the effects of computerized cognitive training on anxiety, sleep, mental abilities (cognition), and other aspects of daytime functioning, such as arousal.

Interventions

BEHAVIORALCognitive Training

Participants (n=15) will complete computerized cognitive training games and activities online 3 times/week for 8 weeks.

BEHAVIORALTrivia Training

Participants (n=15) will receive computerized trivia questions to answer and submit 3 times/week for 8 weeks.

Sponsors

University of Missouri-Columbia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Intervention model description

Participants will be randomly assigned to cognitive training or trivia training and will complete measures of anxiety, sleep, cognition (objective, self-efficacy), and self-reported arousal at baseline, and post-intervention

Eligibility

Sex/Gender
ALL
Age
45 Years to 59 Years
Healthy volunteers
Yes

Inclusion criteria

* 45-59 yrs of age * no neurological or psychiatric illness, dementia, or loss of consciousness \> 5 mins * nongamers (i.e., report \<1 hour of video/cognitive training games/week over last 2 yrs) * proficient in English (reading and writing) * computer meets technology requirements (i.e. Windows: Windows 7 or above using Internet Explorer 11 or Edge, Mozilla Firefox 41 and above, Google Chrome 48 and above; Mac OS: Mac OS X v10.8 and above using Safari 10 and above, Mozilla Firefox 42 and above, Google Chrome 48 and above; Android App: Android 6 or higher version; iOS App: iOS 10 or higher version * meet clinical dx criteria for Generalized Anxiety Disorder.

Exclusion criteria

* unable to provide informed consent * unable to undergo randomization * Telephone Interview for Cognitive Status-modified (TICS) score \<33, 2) * other sleep disorder (i.e., sleep apnea, Periodic Limb Movement Disorder-PLMD, narcolepsy, REM Sleep Behavior Disorder) * severe untreated psychiatric comorbidity that renders randomization unethical * psychotropic, anxiolytic medications or other medications(e.g., beta-blockers) that alter mood or sleep * uncorrected visual/auditory impairments * participation in nonpharmacological treatment for sleep/fatigue/mood outside the current study.

Design outcomes

Primary

MeasureTime frameDescription
Objective Cognition - Computerized Cognitive TasksUp to 10 weeksComplete computerized tasks. These tasks will measure cognitive functions (e.g., processing speed).
Subjective Cognitive Self-Efficacy. -Cognitive Failures QuestionnaireUp to 10 weeksA 25-item questionnaire. Participants rate from 0 (never) to 4 (very often) frequency of cognitive errors. Higher scores indicate lower cognitive self-efficacy.
Coronavirus Anxiety ScaleUp to 10 weeks5- item questionnaire that assess anxiety related to the Coronavirus.
Anxiety - State-Trait Anxiety InventoryUp to 10 weeksInventory that asks respondents to rate how true 20 self-descriptive statements (e.g., I feel calm) are on a 4-point scale (1 = not at all, 4 = very much so). Typically, respondents are asked to rate statements according to how they generally feel (trait-anxiety scale) and how they feel in the current moment (state-anxiety scale). Total scores range from 20 to 80, with higher scores indicating greater maladjustment.

Secondary

MeasureTime frameDescription
Subjective Arousal- Pre-sleep Arousal ScaleUp to 10 weeksPre-sleep Arousal Scale is a 16-item self-report questionnaire comprising both cognitive and somatic manifestations of arousal.
Subjective Arousal- Arousal Predisposition Scale Subjective Arousal- Arousal Predisposition Scale Subjective Arousal- Arousal Predisposition ScaleUp to 10 weeksArousal Predisposition Scale is a 12-item inventory that has been designed to measure the degree to which an individual experiences arousal. Higher scores indicate greater predisposition to arousal.
Game Engagement QuestionnaireUp to 10 weeksQuestionnaire assessing the experience of the game.
Mood-Depression-Beck Depression Inventory-IIUp to 10 weeks21-item inventory that asks respondents to rate on a scale of 0 (no depressive feelings) to 3 (most depressive feelings) their feelings towards various aspects of daily living/situations. Higher total scores indicate worse depressive symptoms.
Alcohol Use - Alcohol Use Disorder TestBaseline10-item questionnaire that assess the frequency of alcohol use and problems associated with alcohol use over the past year.
Physical Activity - International Physical Activity QuestionnaireUp to 10 weeks7- item questionnaire assessing the different kinds of physical activities that the participant does as pat of their everyday life.
Computer Proficiency- Computer Proficiency QuestionnaireBaselineThis questionnaire asks about participants' ability to perform a number of tasks with a computer. Will be examined as a covariate.
COVID-19 related media exposure and risk questionsUp to 10 weeks20- item questionnaire assessing the effects of news and social media on perception of COVID-19.
Subjective Intervention Efficacy- Internet Intervention Utility QuestionnaireUp to 10 weeks16- item questionnaire about the use of the intervention.
Subjective Behavioral Sleep- Insomnia Severity IndexUp to 10 weeksBrief self-report measure of current perception of insomnia symptom severity, distress and daytime impairment. Commonly used in insomnia treatment outcome research.
Beck Depression Inventory-2nd EditionUp to 10 weeks21-item inventory that asks respondents to rate on a scale of 0 (no depressive feelings) to 3 (most depressive feelings) their feelings towards various aspects of daily living/situations. Higher total scores indicate worse depressive symptoms.
Subjective Behavioral Sleep - Electronic Daily Sleep DiariesUp to 10 weeksOnline diaries completed each morning (\ 5 mins); diaries measure sleep onset latency, wake time after sleep onset, total sleep time, and sleep quality.
Personality - Big Five InventoryBaseline10 question assessment measuring personality.
Game-related experience- Sessions and duration playedUp to 10 weeksDuring the intervention phase the cognitive training group will play games and will need to log the days and duration played.
Circadian Rhythm- Morningness-Eveningness QuestionnaireUp to 10 weeks19-item questionnaire that assesses preference for morning, afternoon, and evening activities. Total score reflects degree of morningness or eveningness type.
Subjective Arousal- Global Cognitive Arousal-Perceived Stress ScaleUp to 10 weeksPerceived Stress Scale is a self-report measure of how life situations are perceived as stressful. The scale consists of 15 items corresponding to everyday situation and participants are asked to rate on a likert scale from 0 (never) to 4 (very often) how often they felt or thought a specific way. Higher scores correspond to higher perceived stress.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026