Actively Recruiting
Long-Covid-19 Alleviation Through Learning Mindfulness Study
Led by Columbia University · Updated on 2025-08-24
400
Participants Needed
1
Research Sites
182 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research is being done to study a mindfulness intervention among people who have symptoms of Post-Acute Sequelae of SARS-CoV-2 infection (PASC), also known as Long COVID. Mindfulness is defined as paying attention to the present moment with non-judgment and acceptance. Here the investigators are studying whether a mindfulness intervention can help reduce stress, reduce Long COVID symptoms, and improve quality of life among people living with Long COVID. The mindfulness intervention is a series of recorded mindfulness sessions, which were created by the study team. People who decide to take part will be randomly assigned to receive the study mindfulness intervention immediately after joining the study or to receive the study mindfulness intervention 8 weeks after joining the study. All participants will continue their usual medical care. Participants will complete online surveys to measure symptoms over time. The study will last 6 months.
CONDITIONS
Official Title
Long-Covid-19 Alleviation Through Learning Mindfulness Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 or older
- Willing and able to provide informed consent
- Access to the internet
- Self-reported history of SARS-CoV-2 infection
- Current symptoms attributed to Post-Acute Sequelae of SARS-CoV-2 infection (PASC) by participant or medical provider; symptoms lasting at least 12 weeks after COVID-19 illness
You will not qualify if you...
- Participating in another clinical trial of an intervention for PASC symptoms
- Currently engaged in a structured mindfulness-based intervention
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Columbia University
New York, New York, United States, 10032
Actively Recruiting
Research Team
D
Deborah Theodore, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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