Official Title
UPright Incline Positioning in COVID-19 Patients for Oxygen SATuration Improvement With Hypoxemic Respiratory Failure (UPSAT)
Brief Summary

COVID-19 is a respiratory illness caused by SARS-CoV-2 with a range of symptoms from mild, self-limiting respiratory tract infections to severe progressive pneumonia, multiorgan dysfunction and death. A portion of individuals with COVID-19 experience life-threatening hypoxia requiring supplemental oxygen and mechanical ventilation. Management of hypoxia in this population is complicated by contraindication of non-invasive ventilation and limitations in access to mechanical ventilation and critical care staff given the clinical burden of disease. Positional therapy is readily deployable and may ultimately be used to treat COVID-19 related respiratory failure in resources limited settings; and, it has been demonstrated to improve oxygenation and is easy to implement in the clinical setting. The overall goal of this randomized controlled trial is to establish the feasibility of performing a randomized trial using a simple, minimally invasive positional therapy approach to improve hypoxia and reduce progression to mechanical ventilation. The objectives are to examine the effectiveness and feasibility of maintaining an inclined position in patients with confirmed or suspected COVID-19 associated hypoxemic respiratory failure. The investigators hypothesize that (1) oxyhemoglobin saturation will improve with therapy, (2) participants will tolerate and adhere to the intervention, and that (3) participants who adhere to positional therapy will have reduced rates of mechanical ventilation at 72 hours. If successful, this feasibility trial will demonstrate that a simple, readily deployed nocturnal postural maneuver is well tolerated and reverses underlying defects in ventilation and oxygenation due to COVID-19. It will also inform the design of a pivotal Phase III trial with estimates of sample sizes for clinically relevant outcomes.

Detailed Description

Study Design: The investigators will conduct a pilot study to examine the acute effects of
inclined posture on oxyhemoglobin saturation and the feasibility of conducting randomized
controlled clinical trial among patients with confirmed or suspected COVID-19-associated

In a subgroup of participants, the investigators will examine the acute effect of postural
therapy (15-degree incline on hospital beds) on oxyhemoglobin saturation among hypoxic
patients to establish a biologic response. The investigators will enroll a subset of
participants (n=16) who will lie supine on hospital beds, which will be placed in the
horizontal (flat) or 15-degree inclined (reverse Trendelenberg) orientation in random order.
During this time, the investigators will continuous record pulse oximetry, pulse rate and
variations in peripheral arterial tone with WatchPAT one devices. Subjects will be visually
monitored for work of breathing during this time. If work of breathing becomes excessive, as
defined as a sustain respiratory rate of >25 and an increase of >5 breaths per minute from
baseline, or oxygenation decreases below 88% for > 30 seconds in the inclined position, then
maneuvers will be stopped. If the patient meets these criteria in the flat position, then the
investigators sit the patient upright, and allow breathing to return to baseline before
examining responses in the inclined position.

The investigators will randomize participants to have beds placed in 15-degree incline or
usual care (ad-lib positioning) for 72 hours. During the first night in a subgroup of
participants, the investigators will record oxygenation, sleep wake state and markers of
sympathetic activity with WatchPAT One devices, which can obtain cardiopulmonary parameters
with high temporal resolution. The investigators will obtain vital signs from the data
warehouse, which archives telemetry data with a maximum sampling frequency of 1 minute. The
investigators will record adherence with continuous accelerometry sensors placed on the bed
rails and on the anterolateral surface of participants' chests to measure bed and
participants' positions, respectively. Aside from position, participants will receive usual
treatment for COVID-19.

The investigators will enroll in 3 phases. At the end of each phase, the investigators will
assess for completion of milestones for proceeding to the subsequent phase, as detailed

1. Pilot Study: The investigators will pilot the study in 16 participants to obtain
critical information on logistics of conducting the trial including performance of
recording instruments in a biocontainment environment, to examine the feasibility of the
intervention, perform preliminary safety evaluations to ascertain potential harm and to
determine whether the intervention results in a meaningful difference in body position.

2. Phase II RCT: If inclined therapy results in a difference in body position and no
significant safety issues were detected, the investigators will conduct a phase II
randomized-controlled trial (RCT) in 70 participants (see sample size calculation below)
to estimate the effect size of inclined position on rates of intubation and determine
sample size for a Phase III trial.

Randomization will be occur in both phases and will be stratified by study phase and study

Hypoxic Respiratory Failure

Other: Postural Positioning

Investigators will adjust the positioning of hospital beds to assess improvements in oxygenation and respiratory status.

Eligibility Criteria

Inclusion Criteria:

- COVID-19 positive

- Pneumonia defined as hospitalization for acute (< 7 days) onset of symptoms (cough,
sputum production, or dyspnea).

- Hypoxemia defined as ≥ 2 L/min oxygen

Exclusion Criteria:

- Intubation

- Inability to lie supine

Eligibility Gender
Eligibility Age
Minimum: 18 Years ~ Maximum: N/A
United States

Johns Hopkins Bayview Hospital
Baltimore, Maryland, United States

Johns Hopkins Hospital
Baltimore, Maryland, United States

Luu Pham, MD, Principal Investigator
Johns Hopkins University

Johns Hopkins University
NCT Number
MeSH Terms
Respiratory Insufficiency