The Long COVID-19 Wearable Device Study

Recruiting now · Not applicable

Conditions studied: Long COVID, Postural Orthostatic Tachycardia Syndrome, Dysautonomia, Myalgic Encephalomyelitis, Chronic Fatigue Syndrome, Long Covid19

In brief

To further characterize Long COVID-19 by collecting data from individuals who already own wearable devices or are provided with a wearable device along with basic and enhanced educational materials to determine if both can improve Long COVID-19 symptom management and post-exertional malaise.

Key facts

Study ID

NCT05741112

Run by

Scripps Translational Science Institute

People needed

100500

Starts

2023-11-16

Expected to finish

2025-12-01

Last updated by the study team

2025-05-11

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Is at least 18 years old.
• Has a self/and or physician diagnosis of:
• Long COVID (based on the WHO working definition),
• ME/CFS (myalgic encephalomyelitis / chronic fatigue syndrome, self-diagnosis based on IOM criteria), and/or
• POTS (Postural Orthostatic Tachycardia Syndrome).
• Is interested in tools to manage ME/CFS, POTS, and/or Long COVID symptoms.
• Owns a wearable device they are willing to use for this study or does not own a device and agrees to utilize a study-provided one.
• Agrees to wear the device throughout the study period, share the data with the study, and sync data at least weekly.
• Has access to a smartphone or tablet to enable syncing wearable data and viewing device feedback.
• Agrees to disclose involvement in other ME/CFS, POTS, and/or Long COVID interventions such as medical treatment, self-management, and other interventional studies.
• Agrees to complete at least 75% of the study surveys.

You may not qualify if…

• As long as they meet inclusion there is no exclusion

Where it is running

• Scripps Research — La Jolla, California, United States (enrolling)

Full record on ClinicalTrials.gov

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