Actively Recruiting
Modifying the Inpatient Environment to Reduce Delirium in Older Adults
Led by Farhaan S. Vahidy · Updated on 2024-12-17
10890
Participants Needed
5
Research Sites
252 weeks
Total Duration
On this page
Sponsors
F
Farhaan S. Vahidy
Lead Sponsor
P
Patient-Centered Outcomes Research Institute
Collaborating Sponsor
AI-Summary
What this Trial Is About
The overall goal is to reduce the incidence and burden of delirium, as measured by the delirium burden index (DBI) among hospitalized older adults (≥70 years), by modifying the inpatient environment to decrease its sleep antagonism. The investigators propose to implement a multi-modal sleep hygiene (MMSH) bundle, an enhancement of a previously reported sleep-focused intervention which had 88 - 100% compliance for intervention components, and reduced ICU delirium by 50%.
CONDITIONS
Official Title
Modifying the Inpatient Environment to Reduce Delirium in Older Adults
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Non-critically ill patients aged 70 years or older
- All sexes
- All races and ethnicities
- Admitted to the specified clinical units participating in the study
You will not qualify if you...
- Patients with active alcohol or substance withdrawal
- Patients with acute psychiatric illness
- Patients initially admitted to intensive care unit or requiring mechanical ventilation
- Patients present on a unit at the time of unit randomization
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 5 locations
1
Houston Methodist Baytown Hospital
Baytown, Texas, United States, 77521
Actively Recruiting
2
Houston Methodist Hospital
Houston, Texas, United States, 77030
Actively Recruiting
3
Houston Methodist Research Institute
Houston, Texas, United States, 77030
Actively Recruiting
4
Houston Methodist West Hospital
Houston, Texas, United States, 77094
Actively Recruiting
5
Houston Methodist Sugarland Hospital
Sugarland, Texas, United States, 77479
Actively Recruiting
Research Team
R
Rejani Nair, BSN
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
PREVENTION
Number of Arms
2
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