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A Study to Evaluate Comorbid Insomnia and Sleep Disordered Breathing in Patients Undergoing Cardiac Rehabilitation

Overview

Información sobre este estudio

The objectives of this study are to examine the prevalence of comorbid sleep disordered breathing (SDB) and insomnia in post-MI patients enrolled in cardiac rehabilitation (CR), to assess whether post-MI CR patients with comorbid SDB and insomnia exhibit a more unfavorable CV profile than those without, and to determine whether post-MI CR patients with comorbid SDB and insomnia show less adherence to CR than those without.

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:

- Patients will be >18 years old

- Referred to CR following admitted to the hospital with a documented diagnosis of acute
coronary syndrome

- Referred to CR following admission to the hospital with a documented diagnosis of ST-
elevation myocardial infarction (STEMI),

- Referred to CR following admission to the hospital with a documented diagnosis of non-
STEMI

- Referred to CR following admission to the hospital with a documented diagnosis of
unstable angina

- Referred to CR following admission to the hospital with a documented diagnosis of post
coronary artery bypass surgery

- Referred to CR following admission to the hospital after percutaneous coronary
intervention (with or without stent placement).

Exclusion Criteria:

- heart failure with reduced ejection fraction

- peripheral artery disease

- valve or pericardial surgery

- heart transplantation

- patients unable to provide informed consent

- patients unable to speak and read English

- night shift workers

- pregnant women

- those who will only attend full home-based CR.

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

Eligibility last updated 8/2/23. 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

Amanda Bonikowske, Ph.D.

Cerrado para la inscripción

Contact information:

Rebecca Jobes

(507) 538-7425

RSTCVRUPrevent@mayo.edu

More information

Publicaciones

Publications are currently not available

Otros temas en investigación

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CLS-20519408

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