Official Title
Cognitive Rehabilitation to Improve Functioning in Veterans Following COVID-19
Brief Summary

Cognitive dysfunction, psychiatric symptoms, functional impairment, and disability following COVID-19 negatively impact Veterans' community functioning and quality of life, contribute to significant human suffering, and are costly to VHA. Rehabilitation is a critical priority for Veterans with long COVID. One promising treatment to improve functioning in Veterans with post-COVID-19 cognitive symptoms is Compensatory Cognitive Training (CCT). Previous studies have found that CCT is feasible, acceptable, and efficacious in Veteran populations with multiple sources of cognitive dysfunction. This randomized controlled trial aims to address important RR&D priorities by examining feasibility, acceptability, and preliminary efficacy of a COVID-19-specific rehabilitation intervention, CCT for long COVID (CCT-C) compared to a robust control condition. The proposed study has the potential to improve cognitive function, functional independence, and quality of life for Veterans with late or delayed effects of secondary conditions related to COVID-19 infections.

Detailed Description

2-8% of the US population report "long COVID" symptoms - including "brain fog," thinking
difficulties, memory problems, and psychiatric symptoms such as sleep disturbance, anxiety,
and depression. Rates of post-COVID-19 symptoms are nearly double in the Veteran population.
These cognitive symptoms contribute to functional impairments, reduced quality of life,
poorer self-reported health status, psychological distress, delayed return to work, new onset
disability, reduced community integration, and increased healthcare utilization. One
promising treatment to improve both everyday functioning and cognition secondary to
post-COVID-19 symptoms is Compensatory Cognitive Training (CCT). Previous studies have found
that CCT is feasible, acceptable, and efficacious in Veteran populations with multiple
sources of cognitive dysfunction. The proposed CDA provides a golden opportunity to evaluate
CCT for Veterans with prolonged COVID-19 symptoms (CCT-C), compared with a robust control
condition, Holistic Cognitive Education (HCE). The project closely aligns with current RR&D
priorities, by "examining COVID-19-specific rehabilitation interventions and responses to
treatment" and by addressing "late or delayed effects of secondary conditions related to
COVID-19 infections on impairment and disability." Specific aims are 1) to conduct a pilot
randomized controlled trial of remote CCT-C with 70 Veterans (35 CCT-C, 35 HCE) with
post-COVID-19 cognitive symptoms to examine feasibility, acceptability, and initial efficacy;
2) to examine the preliminary efficacy of CCT-C in this population on overall functioning, as
measured by the World Health Organization's Disability Assessment Schedule (WHODAS 2.0),
performance-based measures of functional capacity, and secondary outcomes (cognitive
performance, quality of life, self-reported cognitive problems, psychiatric symptoms, sleep
disturbance, and engagement in work/community activities); and 3) to explore moderators of
outcome (e.g., age, initial COVID-19 severity, baseline cognitive functioning, presence of
PTSD/mTBI history; biomarkers related to COVID-19 infection).

Not yet recruiting
Post-acute COVID-19 Syndrome

Behavioral: Compensatory Cognitive Training for COVID-19

CCT-C is a manualized group-based behavioral intervention (10 weeks, 2 hours per week, 20 hours total) designed to improve cognition and everyday functioning in patients with prolonged COVID-19 symptoms
Other Name: CCT-C

Behavioral: Holistic Cognitive Education

HCE provides the same frequency and amount of therapist and other group member contact as CCT-C, but does not provide training in cognitive or lifestyle strategies addressed in CCT-C. The HCE intervention provides information and discussion regarding common causes of and treatments for cognitive impairment.
Other Name: HCE

Eligibility Criteria

Inclusion Criteria:

- Veterans > 18 years old who are able to provide informed consent

- Prior participation in SF Parent Study or LA Parent Study

- Report of cognitive symptoms that Veteran attributes to COVID-19 infection

Exclusion Criteria:

- Current substance abuse disorder, psychotic disorder, dementia, etc.

- History of moderate to severe brain injury with loss of consciousness > 30 minutes

- Auditory or visual impairments that would prevent the ability to participate in
assessment procedures

- Invalid performance on one or more embedded performance validity tests (PVTs)

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: N/A
Countries
United States
Locations

VA San Diego Healthcare System, San Diego, CA
San Diego, California, United States

Investigator: Tara A Austin, AA
Contact: 858-642-3657
tara.austin@va.gov

Investigator: Tara A Austin, AA

Contacts

Tara A Austin, AA
(858) 642-3657
tara.austin@va.gov

Elizabeth W Twamley, PhD
(858) 552-8585 - 3848
etwamley@health.ucsd.edu

Tara A Austin, AA, Principal Investigator
VA San Diego Healthcare System, San Diego, CA

VA Office of Research and Development
NCT Number
Keywords
Post-Acute COVID-19 Syndrome
Cognitive Rehabilitation
Cognitive Training
Cognitive remediation
MeSH Terms
COVID-19
Post-Acute COVID-19 Syndrome