# Study of Postacute Sequelae of COVID-19 Using Digital Wearables: Protocol for a Prospective Longitudinal Observational Study

**Authors:** Sherine El-Toukhy, Phillip Hegeman, Gabrielle Zuckerman, Anirban Roy Das, Nia Moses, James Troendle, Tiffany M Powell-Wiley

PMC · DOI: 10.2196/57382 · JMIR Research Protocols · 2024-08-16

## TL;DR

This study uses digital wearables to track long-term effects of mild COVID-19, aiming to identify patterns in symptoms and physiological data over six months.

## Contribution

The study introduces a decentralized approach using wearables to monitor postacute sequelae of COVID-19 in nonhospitalized patients.

## Key findings

- Wearables can collect physiological data to identify long-term effects of mild COVID-19.
- The study will provide insights into symptom duration and manifestation in nonhospitalized patients.

## Abstract

Postacute sequelae of COVID-19 (PASC) remain understudied in nonhospitalized patients. Digital wearables allow for a continuous collection of physiological parameters such as respiratory rate and oxygen saturation that have been predictive of disease trajectories in hospitalized patients.

This protocol outlines the design and procedures of a prospective, longitudinal, observational study of PASC that aims to identify wearables-collected physiological parameters that are associated with PASC in patients with a positive diagnosis.

This is a single-arm, prospective, observational study of a cohort of 550 patients, aged 18 to 65 years, male or female, who own a smartphone or a tablet that meets predetermined Bluetooth version and operating system requirements, speak English, and provide documentation of a positive COVID-19 test issued by a health care professional within 5 days before enrollment. The primary end point is long COVID-19, defined as ≥1 symptom at 3 weeks beyond the first symptom onset or positive diagnosis, whichever comes first. The secondary end point is chronic COVID-19, defined as ≥1 symptom at 12 weeks beyond the first symptom onset or positive diagnosis. Participants must be willing and able to consent to participate in the study and adhere to study procedures for 6 months.

The first patient was enrolled in October 2021. The estimated year for publishing the study results is 2025.

This is a fully decentralized study investigating PASC using wearable devices to collect physiological parameters and patient-reported outcomes. The study will shed light on the duration and symptom manifestation of PASC in nonhospitalized patient subgroups and is an exemplar of the use of wearables as population-level monitoring health tools for communicable diseases.

ClinicalTrials.gov NCT04927442; https://clinicaltrials.gov/study/NCT04927442

DERR1-10.2196/57382

## Linked entities

- **Diseases:** COVID-19 (MONDO:0100096), long COVID-19 (MONDO:0100233)

## Full-text entities

- **Diseases:** PASC (MESH:D000094024), COVID-19 (MESH:D000086382)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

150 references — full list in the complete paper: https://tomesphere.com/paper/PMC11364950/full.md

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Source: https://tomesphere.com/paper/PMC11364950