Amygdala Insula Retraining in the Management of Long COVID Symptoms
NCT ID: NCT05851846
Last Updated: 2023-05-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
NA
130 participants
INTERVENTIONAL
2023-05-15
2024-06-15
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Cognitive Rehabilitation for Post-COVID-19 Cognitive Impairment
NCT05498493
Mind-Body Rehabilitative Program for Veterans With mTBI (Mild Traumatic Brain Injury)
NCT01975857
Dual-task Assessment and Rehabilitation for Individuals With Residual Symptoms After mTBI
NCT03478059
Working Memory and Physical Exercise Training in Patients With Mild Cognitive Impairment
NCT05948930
Compensatory Training to Support Brain Healthy Lifestyle Changes in Those at Risk for Alzheimer's Disease
NCT04118985
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
SEQUENTIAL
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Intervention
Mind body intervention + Usual care: The intervention will be delivered virtually
Amygdala insula retraining
Mind body intrevention
Control arm
The participants in the comparator group will be wait listed for the intervention
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Amygdala insula retraining
Mind body intrevention
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
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.
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Miami VA Healthcare System
FED
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Leonardo Tamariz
Staff physician
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Institute for Neuroimmune Medcince
Fort Lauderdale, Florida, United States
Miami VAHS
Miami, Florida, United States
Institute for Neuroinmune medicine
Miami, Florida, United States
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Irina Rozenfeld, ARNP
Role: primary
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
1677529-1
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.