Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID07140094

Long-Covid-19 Alleviation Through Learning Mindfulness Study (LONG-CALM)

Led by Columbia University · Updated on 2025-08-24

400

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating a mindfulness intervention for people experiencing symptoms of Post-Acute Sequelae of SARS-CoV-2 infection (PASC), commonly known as Long COVID. This study aims to determine if mindfulness, defined as paying attention to the present moment with acceptance and without judgment, can help reduce stress, lessen Long COVID symptoms, and improve quality of life. Mindfulness-Based Interventions have been shown in other studies to reduce stress in various populations, suggesting potential benefits for those with PASC. The study involves an 8-week online mindfulness program consisting of recorded sessions specifically developed for people with PASC. Participants are randomly assigned to either receive the mindfulness intervention immediately along with their usual medical care or to start the intervention eight weeks after enrollment while continuing their regular treatment. All participation is remote, with no in-person visits. Participants will complete four online surveys over six months to assess symptoms and quality of life. The main outcome measured is the Patient-Reported Outcomes Measurement Information System (PROMIS) Global 10 Score at two months. Additional assessments include symptom scores related to PASC, depression, anxiety, stress impact, and mindfulness during physical activity. The total study duration is six months, with all data collected remotely to monitor changes over time.

CONDITIONS

Brief Title

Long-Covid-19 Alleviation Through Learning Mindfulness Study

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age �3E 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 �3E= 12 weeks after Covid-19 illness
Not Eligible

You will not qualify if you...

  • Participating in another clinical trial of an intervention for PASC symptoms
  • Engaged in a structured MBI

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (remote)

Treatment

Duration - 8 weeks

Participants receive an 8-week online mindfulness intervention consisting of recorded sessions designed to reduce stress and symptoms of Post-Acute Sequelae of SARS-CoV-2 infection (PASC).

Access sessions online at participant's convenience

Follow-up

Duration - 6 months

Participants complete four online surveys over 6 months to assess symptoms and quality of life after the mindfulness intervention.

4 online survey assessments

Trial Site Locations

Total: 1 location

1

Columbia University

New York, New York, United States, 10032

Actively Recruiting

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Research Team

D

Deborah Theodore, MD

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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