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Clinical Trials/NL-OMON24132
NL-OMON24132
Recruiting
Not Applicable

Identification of stressors and de-stressors in employees working from homeduring COVID-19: an observational study with the use of consumer wearables

Stichting imec Nederland0 sites200 target enrollmentTBD
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Conditionsone

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
one
Sponsor
Stichting imec Nederland
Enrollment
200
Status
Recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational non invasive

Investigators

Sponsor
Stichting imec Nederland

Eligibility Criteria

Inclusion Criteria

  • •Subjects between 18 and 65 years old
  • •\- Subjects working for at least 4 days during the 7 days in total, from which at least 3 days are spend working from home. Each workday must consist of at least 6 hours a day
  • •\- Subjects are working/residing in the United States during the measurements
  • •\- Subjects capable of wearing a wrist\-worn tracker on one of their wrists
  • •\- Subjects must have a smartphone newer than 2014 that runs iOs 11\+ or Android 7\.0\+ which is continuously available to them during the whole duration of the experiment.
  • •\- Subjects must be capable of using a smartphone app
  • •\- Subjects must have English working proficiency.

Exclusion Criteria

  • •\- Subjects being incapable (for whatever reason) to properly read/understand/sign the informed consent and subject information.
  • •\- Subjects with known atherosclerosis and/or cardiovascular impairments.
  • •\- Subjects with a known medical condition that will increase risk of infections due to the electrodes like for example wounds on hand and arm or skin allergies.
  • •\- Subjects with a known allergy to silicone.
  • •\- Subjects wearing any other measuring device which cannot be removed (i.e. Holter monitor).
  • •\- Patients with known sensitivity to light or using medication with phototoxic side ef\-fects (i.e. Tetracycline, Doxycycline, Phenothiazines, Dacarbazine, Ketoprofen, Lomefloxacin). This is in order to exclude the possibility of local skin irritation from prolonged irradiation by LED\-light (from the wearable on the wrist).
  • •\- Women known to be pregnant.
  • •\- Subjects with any implanted active device (i.e.,. device containing a battery), such as a pacemaker.
  • •\- Subjects with epilepsy or known sensitivity to bright light
  • •\- Subjects with known nervous system disorders.

Outcomes

Primary Outcomes

Not specified

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