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The ARISE Study - Use of Vertical Positioning

The Arise Study - Use of Vertical Positioning

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07025421
Acronym
ARISE
Enrollment
40
Registered
2025-06-17
Start date
2025-08-25
Completion date
2028-08-31
Last updated
2026-08-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Respiratory Distress Syndrome

Keywords

Bed Position

Brief summary

The pilot study will randomize 40 ARDS patients who if proning were required would be randomized to upright bed positioning or to stand of care with bed in the head of bed elevation position

Detailed description

Patients will be randomized to receive either daily upright bed positioning or to receive standard of care with head of bed elevated.

Interventions

OTHERIntervention Upright Bed positioning

Patient in receipt of the upright bed positioning will receive daily upright bed positioning time each day of mechanical ventilation following the time required by institutional protocol for ARDS - associated prone positioning

Sponsors

University of Alabama at Birmingham
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

\- Acute Respiratory Distress Syndrome

Exclusion criteria

* Cancer * Active tracheostomy

Design outcomes

Primary

MeasureTime frameDescription
Change in Tidal Volumewithin first 7 days of mechanical ventilationMechanical Ventilator Tidal Volume

Countries

United States

Contacts

CONTACTpeter morris, md
pmorris@uabmc.edu205-934-5548

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 28, 2026