Digital Rehabilitation Environment Augmenting Medical System (DREAMS)

  • STATUS
    Recruiting
  • End date
    Dec 9, 2023
  • participants needed
    100
  • sponsor
    University of Florida
Updated on 9 July 2022
critical illness
confusion

Summary

D.R.E.A.M.S. will assess an immersive digital reality-augmenting system in reducing the occurrence of cognitive, behavioral, and emotional consequences of critical illness and environmental exposures that are risk factors for the development of delirium.

Description

The purpose of Digital Rehabilitation Environment Augmenting Medical System (D.R.E.A.M.S.) is to research the feasibility and clinical potential of an immersive digital reality-augmenting system in reducing the occurrence of cognitive, behavioral, and emotional consequences of critical illness (e.g. pain, anxiety and insomnia) and environmental exposures (noise & light) that are risk factors for the development of delirium, a common and devastating complication in the intensive care unit (ICU).

Details
Condition Delirium
Treatment Technology based guided meditation and relaxation
Clinical Study IdentifierNCT03385993
SponsorUniversity of Florida
Last Modified on9 July 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

All patients ≥ 18 years admitted to University of Florida (UF) Health Shands Hospital who do not have a positive Confusion Assessment Method (CAM) score, including ICU patients

Exclusion Criteria

The study team will exclude patients if
Their anticipated ICU stay is less than one day
Patient is intubated and cannot communicate
Age: < 18 years
Patient with recent (within 6 months) neuro-vascular event, intra-cranial surgery, and/or acute neurological condition as primary ICU admission reason
Baseline cognitive impairment (e.g., advanced dementia)
Patients who are unable to wear or use the DREAMS equipment
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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