Stress can be detected based on physiological parameters and self-reports
ID
Bron
Verkorte titel
Aandoening
None
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Determine stressors and de-stressors in employees working from home
Achtergrond van het onderzoek
This is a low risk, observational study. All subjects will be equipped with a wrist-worn consumer wearable that continuously measures physiological signals (i.e. HR, movements, sleep) together with an accompanying app installed on the participant’s phone. The study will take 7 consecutive days per subject. Subjects will be asked to install another app on their smartphone that prompts short questionnaires 5 times a day at predetermined times. These questionnaires measure subjective experiences and work situations. Subjects can follow their normal daily routines. An additional pre- and post-experiment questionnaire will focus on general subject characteristics and their opinions on the study.
Doel van het onderzoek
Stress can be detected based on physiological parameters and self-reports
Onderzoeksopzet
The device will be worn for 7 days, questionnaires will be prompted 5 times a day with an additional questionnaire before and after the measurement week
Onderzoeksproduct en/of interventie
Daily questionnaires and continuously wearing a consumer wrist-worn sensor
Publiek
Wetenschappelijk
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
- 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.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
- 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.
- Subjects with known mental disorders
- Subjects in therapy or taking medication for psychiatric disorders
Opzet
Deelname
Voornemen beschikbaar stellen Individuele Patiënten Data (IPD)
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
| Register | ID |
|---|---|
| NTR-new | NL9378 |
| Ander register | WCG IRB : 20210874 |