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Psychotherapy for Long COVID
N/A
Waitlist Available
Led By Marianne S. Goodman, MD
Research Sponsored by VA Office of Research and Development
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Ages 18-80
Be older than 18 years old
Must not have
Lack of capacity to consent
MINI Mental Status < 23 or inability to function in a group setting
Timeline
Screening 3 weeks
Treatment Varies
Follow Up this outcome will be measured at 2 time points: consent & baseline and immediately post intervention (after the second 8 sessions)
Awards & highlights
No Placebo-Only Group
Summary
This trial tests a therapy program called Long COVID Coping and Recovery (LCCR) for Veterans with Long COVID. The program aims to help them manage their symptoms and improve mental health through group sessions that teach coping skills and build resilience. The goal is to see if the program is feasible and beneficial for Veterans.
Who is the study for?
This trial is for U.S. Veterans aged 18-80 with Long COVID, who are clinically stable to join group therapy and use VA services at the JJPVAMC. Participants must have had a positive COVID-19 test and symptoms lasting over a month. Those with severe mental impairment, inability to engage in groups, or active substance dependence can't join.
What is being tested?
The LCCR Intervention is being tested for its ability to help veterans cope with Long COVID by improving psychological adjustment, resilience, and coping skills using established psychotherapeutic techniques in a group setting.
What are the potential side effects?
As this is a psychotherapeutic intervention focusing on mental health recovery rather than medication or medical procedures, traditional physical side effects are not expected; however emotional discomfort may arise as part of the therapeutic process.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am between 18 and 80 years old.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am unable to understand and make decisions about my health care.
Select...
I may have trouble thinking, remembering, or being in groups.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ this outcome will be measured at 2 time points: consent & baseline and immediately post intervention (after the second 8 sessions)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~this outcome will be measured at 2 time points: consent & baseline and immediately post intervention (after the second 8 sessions)
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in Functional Improvement Post-COVID-19 Over Time
Secondary study objectives
Change in Anxiety Over Time
Change in Depression Over Time
Change in Health-Related Functional Status Over Time
+5 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Long COVID Coping and Recovery (LCCR) InterventionExperimental Treatment1 Intervention
Veterans will participate in a LCCR (1x/week for a total of 16 sessions) via the HIPAA-compliant telehealth platform VA Video Connect (VVC) and/or VA WebEx with two co-therapists.
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for COVID-19 include antiviral agents, steroids, and immunomodulators, which work by reducing viral replication, inflammation, and modulating the immune response. Non-pharmacologic treatments, such as those studied in the Long COVID Coping and Recovery (LCCR) trial, focus on psychotherapeutic interventions aimed at improving psychological adjustment, promoting resilience, and facilitating coping.
These interventions are crucial for managing long-term effects like anxiety, depression, and stress-related disorders, addressing both physical and mental health challenges to improve overall patient outcomes.
Long-COVID and Stress Overload: A Direct Link with Psychophysical Disease. A Necessary Interconnection to Focalize Emerging Needs and Necessities.Management and treatment of long COVID symptoms in general practices: An online-based survey.Post-COVID-19 acute sarcopenia: physiopathology and management.
Long-COVID and Stress Overload: A Direct Link with Psychophysical Disease. A Necessary Interconnection to Focalize Emerging Needs and Necessities.Management and treatment of long COVID symptoms in general practices: An online-based survey.Post-COVID-19 acute sarcopenia: physiopathology and management.
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Who is running the clinical trial?
VA Office of Research and DevelopmentLead Sponsor
1,658 Previous Clinical Trials
3,361,626 Total Patients Enrolled
15 Trials studying COVID-19
410,334 Patients Enrolled for COVID-19
Marianne S. Goodman, MDPrincipal InvestigatorJames J. Peters Veterans Affairs Medical Center
2 Previous Clinical Trials
284 Total Patients Enrolled
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Eligibility Criteria:
This trial includes the following eligibility criteria:- I am unable to understand and make decisions about my health care.You currently have severe mental health issues that are not stable.I may have trouble thinking, remembering, or being in groups.My doctor thinks I'm ready for group therapy.You are currently dependent on alcohol or opioids and need medical help to stop.I am between 18 and 80 years old.I have been diagnosed with Long COVID.
Research Study Groups:
This trial has the following groups:- Group 1: Long COVID Coping and Recovery (LCCR) Intervention
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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