No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
400 (estimated)
Sponsor
Columbia University · Other
Who this trial is looking for
This trial is looking for adults who have been experiencing Long COVID symptoms. Participants will either start a mindfulness program right away or after 8 weeks, while continuing their regular medical care.
Are You a Good Fit for This Trial?
You may be able to join if
I am 18 years or older
I can provide informed consent
I have access to the internet
I have a history of SARS-CoV-2 infection
I have symptoms that have lasted 12 weeks or more after my COVID-19 illness
You may not be able to join if
I am participating in another clinical trial for Long COVID symptoms
I am engaged in a structured Mindfulness-Based Intervention (MBI)
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
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, an…
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.
Trial Locations
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City
State
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Status
Eligibility Criteria
Inclusion Criteria:
* Age \> or = 18
* Willing and able to provide informed consent
* Access to the internet
* Self-reported history of SARS-CoV-2 infection
* Current symptoms attributed to PASC by participant or by participant's medical provider; ongoing symptoms that persisted \>= 12 weeks after …
Inclusion Criteria:
* Age \> or = 18
* Willing and able to provide informed consent
* Access to the internet
* Self-reported history of SARS-CoV-2 infection
* Current symptoms attributed to PASC by participant or by participant's medical provider; ongoing symptoms that persisted \>= 12 weeks after Covid-19 illness
Exclusion Criteria:
* Participating in another clinical trial of an intervention for PASC symptoms
* Engaged in a structured MBI
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