A Study to Evaluate How Cognitive Performance and Physiological Measures Change After Acute Stress

Overview

Información sobre este estudio

The purpose of the current research study is to understand how physiological measures, cognitive performance, and self-report of perceived stress change after acute stress and how different features of a relaxation room promote recovery after stress.

 

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

Inclusion Criteria:

  • Adults at least age 18.
  • Participants are able to remain in the Well Living Lab for 3-4 hours.
  • Participants are able to perform scripted tasks.
  • Participants are able to provide informed consent
  • Participants are able to wear the wearable devices at all times during the study
  • Participants have completed a COVID vaccine regimen and can provide written documentation verifying vaccination status at least fourteen (14) days prior to the commencement of the research study.

Exclusion Criteria:

  • Participants with a reported history of diagnosed mood, anxiety, or major health disorders.
  • Participants who have used steroid-based medications within the past three years.
  • Participants with a history of drug/alcohol abuse.
  • Participants with or recovering from nicotine dependency who cannot use a nicotine patch.
  • Participants who consume excessive amounts of caffeine.
  • Participants who have had severe sleep disturbance (e.g., shift work, chronic insomnia).
  • Women who are pregnant or intend to become pregnant at the time of the study.
  • Participants with a history of diagnosed cognitive impairment.
  • Participants taking any medications that might affect the physiological measures of interest.
  • Participants with anything that might affect collecting the physiological measures of interest (e.g., cosmetic products, head coverings, head products, etc.).

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus

Rochester, Minn.

Investigador principal de Mayo Clinic

Colin West, M.D., Ph.D.

Cerrado para la inscripción

More information

Publicaciones

Publications are currently not available
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CLS-20523326

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