Actively Recruiting
Mind Body Intervention for Long COVID-19
Led by Beth Israel Deaconess Medical Center · Updated on 2026-02-18
180
Participants Needed
1
Research Sites
159 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this study is to determine if a mind-body intervention can help people suffering from symptoms associated with Long COVID. The study is a randomized trial examining the effectiveness of a mind body intervention in reducing somatic symptoms from Long COVID in participants as compared to usual care and an active control (second mind body intervention). The investigators will secondarily investigate whether the intervention alleviates individual somatic complaints and improves daily functioning, relative to usual care and the active control
CONDITIONS
Official Title
Mind Body Intervention for Long COVID-19
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 years or older
- Confirmed infection with SARS-CoV-2 by antibody, antigen, or PCR test
- Symptoms attributed only to COVID-19, not to other known diseases
- Somatic Symptom Score-8 score of 10 or higher involving at least 3 symptom areas
- Symptoms present at least 3 days per week for at least 3 months
- Willingness to participate in a mind-body intervention
You will not qualify if you...
- Diagnosis of a clear physical disease such as lung fibrosis or myocarditis (excluding mild arthritis)
- Hospitalization in an intensive care unit for acute COVID-19 infection
- Age over 65 years
- Diagnosis of dementia or similar cognitive impairment
- Active addiction disorder interfering with participation
- Major psychiatric disorders like schizophrenia (mild to moderate anxiety and depression allowed)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Beth Israel Deaconess Medical Center
Boston, Massachusetts, United States, 02115
Actively Recruiting
Research Team
A
Ashley Scafetta
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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