RecruitingNot ApplicableNCT05741112

The Long COVID-19 Wearable Device Study


Sponsor

Scripps Translational Science Institute

Enrollment

100,500 participants

Start Date

Nov 16, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

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.


Eligibility

Min Age: 18 Years

Inclusion Criteria11

  • 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.

Exclusion Criteria1

  • As long as they meet inclusion there is no exclusion

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Interventions

DEVICEWearable device

The treatment group will receive their wearable device and the enhanced education at the start of the study. Their outcomes will be compared with the control group who will receive at 3 months.


Locations(1)

Scripps Research

La Jolla, California, United States

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NCT05741112


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