Effect of Apollo Wearable on Long COVID-19 Symptoms.

Description

The purpose of this study is to examine how Apollo wearable use impacts symptoms and quality of life following long COVID.

Conditions

Post-acute Sequelae of SARS-COV-2 Infection

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Study Overview

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Study Details

Study overview

The purpose of this study is to examine how Apollo wearable use impacts symptoms and quality of life following long COVID.

Effect of Apollo Wearable on Symptoms Related to Post-acute Sequelae SARS-CoV-2 Infection (PASC).

Effect of Apollo Wearable on Long COVID-19 Symptoms.

Condition
Post-acute Sequelae of SARS-COV-2 Infection
Intervention / Treatment

-

Contacts and Locations

Pittsburgh

The Board of Medicine, Pittsburgh, Pennsylvania, United States, 15219

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * New purchasers of Apollo who haven't started using their Apollo device or previous users of Apollo who haven't used Apollo in the preceding 14 days.
  • * Age 18 years or over
  • * Currently experiencing symptoms related to long-COVID according to PASC (self report).
  • * Must be experiencing PASC symptoms in at least one of the following domains:
  • * Inability to use or access a compatible Android or iOS smartphone
  • * Are unable to complete consent and questionnaires written in English
  • * Current resident of a European Union (EU) country

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

The Board of Medicine,

Study Record Dates

2025-03