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Search / Trial NCT04536623

SIESTA for Acute Stroke Rehabilitation

Launched by · Aug 28, 2020

Trial Information

Current as of August 19, 2025

Recruiting

Keywords

Wearable Sensors Quality Indicator (Qi) Score Acute Stroke Rehabilitation Sleep Disordered Breathing (Sdb)

ClinConnect Summary

The SIESTA for Acute Stroke Rehabilitation trial is studying how two sleep-related approaches can help patients recovering from a stroke. The goal is to create a more restful environment for patients by training nurses to minimize unnecessary interruptions and by checking for and treating any sleep problems, like sleep-disordered breathing. Researchers want to see if these methods improve patients' overall recovery and quality of life compared to the usual care they receive in the hospital.

To participate in this trial, individuals must be at least 18 years old and have been diagnosed with a stroke while staying at the Shirley Ryan AbilityLab. They also need to have their doctor's approval to join the study and must be able to give their written consent. However, those with certain serious heart or neurological conditions, pregnant or nursing individuals, and those with specific skin issues or implanted heart devices cannot take part. Participants can expect to receive personalized care focused on improving their sleep and recovery during their hospital stay.

Gender

All

Eligibility criteria

  • Inclusion Criteria:
  • individuals diagnosed with stroke admitted to the Shirley Ryan AbilityLab (inpatient)
  • medical clearance from physician
  • age 18 or older
  • able and willing to give written consent and comply with study procedures
  • Exclusion Criteria:
  • serious cardiac conditions or neurological degenerative pathologies as comorbidities (such as multiple sclerosis, Alzheimer's disease, Parkinson's disease, etc.)
  • pregnant or nursing
  • skin allergies or irritation; open wounds
  • utilizing a powered, implanted cardiac device for monitoring or supporting heart function (i.e. pacemaker, defibrillator, or LVAD)

About

No description available.

Locations

Chicago, Illinois, United States

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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