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In Situ Remote Monitoring in Older Patients at Risk of Stroke

Overview

Información sobre este estudio

The purpose of this study is to examine the relationship between stroke risk stratification categories, according to ABCD2 scoring and post-ischemic stroke status, and passively- and actively collected data (from a smartphone application). Also, to investigate patterns of changes in behavioral and physiological states associated with a stroke event. Addtionally, to explore whether digital phenotyping can provide a valid, useful method for tracking behavioral and physiological changes over time. If our proposed protocol is validated, it has the potential to be applied in both clinical and research settings to improve stroke screening for older adults

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:

  • Men and women between the ages of 18 and 100. 
  • Must present with TIA or IS symptoms and be classified as at risk of stroke using the ABCD2 scoring methodology OR be already recently diagnosed with IS (permanent ischemic lesion).
  • Able to use a smartphone.
  • Report at least moderate smartphone use. 

Exclusion Criteria:

  • Aged < 18 and > 100 at time of enrollment.
  • Heart rate monitoring medications.
  • History of insomnia.
  • History of panic disorder.
  • History of severe anxiety.
  • History of severe depression.
  • BMI > 35.
  • Past or current substance use disorder.
  • Urinary incontinence.
  • Alzheimer’s disease.
  • Borderline personality disorder.
  • Antisocial personality disorder.
  • Dementia.
  • Pre-existing brain and/or cognitive disorder.
  • Cane/walker/wheelchair use:
    • Unstable or acute medical conditions.

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 11/7/23. Questions regarding updates should be directed to the study team contact.

 

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 Contacto

Rochester, Minn.

Investigador principal de Mayo Clinic

Bradley Erickson, M.D., Ph.D.

Abierto para la inscripción

Contact information:

Stephanie Zawada

(480) 301-8000

Zawada.Stephanie@mayo.edu

Jacksonville, Fla.

Investigador principal de Mayo Clinic

Benjamin Pollock, Ph.D., M.S.

Abierto para la inscripción

Contact information:

Stephanie Zawada

(480) 301-8000

Zawada.Stephanie@mayo.edu

Scottsdale/Phoenix, Ariz.

Investigador principal de Mayo Clinic

Bart Demaerschalk, M.D.

Abierto para la inscripción

Contact information:

Stephanie Zawada

(480) 301-8000

Zawada.Stephanie@mayo.edu

More information

Publicaciones

Publications are currently not available

Otros temas en investigación

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CLS-20566542

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