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Modifying the Inpatient Environment to Reduce Delirium in Older Adults
NCT06736951 · View on ClinicalTrials.gov ↗
Study Summary
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 Studied
Interventions
- OTHER MMSH (Multi-Modal Sleep Hygiene) Bundle
Study Locations (5)
Texas
- Houston Methodist Baytown Hospital — Baytown
- Houston Methodist Hospital — Houston
- Houston Methodist Research Institute — Houston
- Houston Methodist West Hospital — Houston
- Houston Methodist Sugarland Hospital — Sugarland
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 10,890 participants |
| Start Date | 2024-06-01 |
| Est. Completion | 2029-03-31 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06736951
The ClinicalTrials.gov registry entry for NCT06736951 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 10,890 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Farhaan S. Vahidy, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Delirium appearing as the primary indexed condition, and to 1 intervention — of which MMSH (Multi-Modal Sleep Hygiene) Bundle is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06736951 reports 5 study locations spanning 1 distinct geographic area — top geographies include Texas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06736951 about?
NCT06736951 is a clinical study titled "Modifying the Inpatient Environment to Reduce Delirium in Older Adults". 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 ...
What is the current status of trial NCT06736951?
This trial is currently recruiting. It is a NA study. The enrollment target is 10,890 participants. The study started on 2024-06-01. Estimated completion is 2029-03-31.
What conditions does trial NCT06736951 study?
This clinical trial studies the following conditions: Delirium, Sleep Hygiene. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06736951?
The interventions under investigation include: MMSH (Multi-Modal Sleep Hygiene) Bundle (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06736951?
This trial is sponsored by Farhaan S. Vahidy, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06736951 being conducted?
This trial has 5 study locations across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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