Amygdala Insula Retraining in the Management of Long COVID Symptoms

NCT ID: NCT05851846

Last Updated: 2023-05-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

130 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-05-15

Study Completion Date

2024-06-15

Brief Summary

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The goal of the study is to compare a mind body intervention against usual care in patients with fatigue with long COVID.

Our research questions include

1. Is the mind body intervention additive to usual care in long COVID
2. Can the mind body intervention change laboratory markers, heart rate variability and dysautonomia.

Detailed Description

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More than 30 percent of the over 70 million individuals in the United States who experienced an acute COVID-19 infection as a result of severe acute respiratory coronavirus-2 (SARS-CoV2), have variety of lingering and disabling symptoms that last beyond the acute phase of the illness. \[1\]This condition is referred to as Post-Acute Sequalae SARS-CoV-2 infection (PASC). Symptoms (including fatigue, post-exertional malaise (PEM), cardiovascular dysfunction, respiratory distress, gastrointestinal disturbances, and dermatologic issues) associated with PASC vary and can affect multiple organ systems. These symptoms are similar to, in extent and degree, to other neuro-immune conditions such as Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS). PASC, as with ME/CFS, is likely to pose a significant impact on the healthcare system and patient's quality of life. An unmet need exists as the susceptibility and pathogenesis of PASC remains yet to be fully elucidated. Emerging evidence suggests that existing interventions widely used for other neuro-immune conditions may prove equally effective in the treatment of PASC. Repurposing of drugs or identification of new drugs will take time. Still, there is growing evidence of the mind-body connection in modulating the autonomic, central and peripheral nervous systems as well as the immune system and the gastrointestinal tract. Recent studies have documented that holistic strategies such as mindfulness, meditation, and amygdala and insula retraining (AIR) have an objective measurable effect on heart rate variability, fatigue, pain, quality of life, depression, anxiety, and gastrointestinal symptoms. The mechanisms proposed include activation of vagus nerve, balancing the autonomic nervous system, reducing stress, and improving immune function. AIR is based on the principle that viral, bacterial, or environmental insults can sensitize the amygdala, which becomes hypervigilant and unleashes a cascade of hormonal responses that perpetuate a state of neuroinflammation and dysautonomia. AIR de-sensitizes the amygdala, breaking vicious cycles and reducing the maladaptive release of hormones and cytokines. Our clinical group has already recommended the use of AIR with great anecdotical response in clinical practice. This strategy is readily available and has no contraindications or risks. We aim to conduct a pilot study of AIR to generate preliminary data for a larger, federally funded trial. Our specific aims are:

1. Identify 130 subjects within the Miami Veteran's Administration (VA) Medical Center who experienced an acute COVID-19 infection and continue to experience persistent moderate fatigue (using standard questionnaires). Subjects will be randomized to either 1. AIR + standard of care or 2. Standard of care/wait list. Individuals in this latter arm will be waitlisted to receive the AIR intervention after they complete the study.
2. Collect standard questionnaires recommended by the Veterans Affairs Healthcare System at baseline, three, and six months to capture levels of fatigue (primary outcome), post exertional malaise (PEM), brain fog, pain, and other symptoms and compare changes over time across the two study arms.
3. Collect objective biometric data in a sample of patients at baseline and at three and six months to explore potential mediating mechanisms: heart rate variability, heart rate and blood pressure sitting and standing, inflammatory markers (c-reactive protein, cortisol, and Epstein Barr viral reactivation. The laboratory tests will not be collected for research purposes as they are collected for clinical purposes.

Conditions

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Long COVID

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SEQUENTIAL

What list of participants
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Intervention

Mind body intervention + Usual care: The intervention will be delivered virtually

Group Type EXPERIMENTAL

Amygdala insula retraining

Intervention Type BEHAVIORAL

Mind body intrevention

Control arm

The participants in the comparator group will be wait listed for the intervention

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Amygdala insula retraining

Mind body intrevention

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

1. Fulfill the definition of PASC
2. Be a patient in the Miami VA post COVID clinic
3. Have access to a computer or phone
5. A probable or confirmed diagnosis of acute COVID-19 infection as per WHO guidelines.
6. Have no evidence of cardiac or pulmonary end organ damage, as per WHO definition. We will define not having end organ damage as a normal ejection fraction on echocardiogram and no pulmonary infiltrates on a non-contrast computed tomography (CT) of the chest during the work-up of the long COVID clinic.
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Miami VA Healthcare System

FED

Sponsor Role lead

Responsible Party

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Leonardo Tamariz

Staff physician

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Institute for Neuroimmune Medcince

Fort Lauderdale, Florida, United States

Site Status

Miami VAHS

Miami, Florida, United States

Site Status

Institute for Neuroinmune medicine

Miami, Florida, United States

Site Status

Countries

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United States

Central Contacts

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Leonardo Tamariz, MD

Role: CONTACT

305-575-7000 ext. 4487

Facility Contacts

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Irina Rozenfeld, ARNP

Role: primary

954-262-2876

Leonardo Tamariz, MD

Role: primary

305-575-7000 ext. 4487

Irina Rozenfeld, ARNP

Role: primary

Other Identifiers

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1677529-1

Identifier Type: -

Identifier Source: org_study_id

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