Skip to content

Proning Early in Awake COVID-19 Hypoxic Respiratory Failure (PREACHR) Study

Proning Early in Awake COVID-19 Hypoxic Respiratory Failure (PREACHR) Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05130541
Acronym
PREACHR
Enrollment
219
Registered
2021-11-23
Start date
2020-06-01
Completion date
2021-05-01
Last updated
2021-11-23

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

Conditions

Covid19, Respiratory Failure

Brief summary

The aim of this proposal is to study whether proning, a technique that has previously been shown to improve lung function in patients with acute respiratory distress syndrome (ARDS), can prevent those with mild to moderate symptoms of COVID-19 from progressing to severe disease when initiated early, thereby averting intubation, reducing hospitalization, and, ultimately, decreasing mortality.

Detailed description

COVID-19 is a global pandemic caused by the novel coronavirus SARS-COV-2. At this time, SARS-CoV-2 is believed to infect alveolar cells, directly impairing lung function and eliciting a profound inflammatory response that further damages the lungs. Between 1 in 20 and 1 in 10 patients infected with this virus die. A crucial decision point in the treatment of patients with COVID-19 in the Emergency Department is the decision to admit to the hospital for further treatment, or discharge the moderately symptomatic (hypoxic and feel ill) but not critically ill patients. However, patients who present with initially mild to moderate symptoms may progress to severe disease. There is, therefore, an unmet need to identify interventions that prevent progression to critical illness in moderately symptomatic patients. Anecdotal reports from Emergency Physicians suggest that alternating prone and supine positioning (i.e. instructing the patient to periodically turn over) improves hypoxia and delays intubation. Dubbed proning, this technique improves hypoxia in 6-7 out of 10 intubated patients with severe acute respiratory distress syndrome (ARDS). Alternating supine and prone positioning improves the recruitment of alveoli, improves ventilation-perfusion matching, increases end-expiratory lung volumes, and improves pulmonary lymphatic drainage. This proposal is innovative because it studies the extension of an intervention previously restricted to patients in the intensive care units with severe acute respiratory distress syndrome (ARDS). Current literature on proning in awake patients with ARDS is limited to retrospective studies with no randomized controlled trials. Further, no clinical trials to date have explored the benefits of early awake proning in COVID-19. The development of a treatment that prevents disease progression and hospitalization in patients moderately ill with COVID-19 would decrease morbidity and mortality from COVID-19 as well as decrease the utilization of scarce healthcare resources. In addition, this trial would be the first randomized controlled-trial, contributing significantly to the nascent evidence base on treatment for COVID-19.

Interventions

BEHAVIORALProning

Rotating on long axis 90 degrees every 30 minutes

OTHERSupportive Care

Usual Care

Sponsors

New York Hospital Queens
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Randomized Controlled Non-Blinded

Eligibility

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

Inclusion criteria

* Age \>18 * Presenting to the ED with symptoms suggestive of COVID-19 * Assessed by ED attending physician to not require emergent intubation * Normal mental status and ability to communicate symptoms/distress * Able to follow instructions independently

Exclusion criteria

* Severe respiratory distress requiring immediate intervention * Unable to follow verbal instructions * Unable to communicate their needs, symptoms, or distress * Inability to tolerate prone positioning due to mental status or habitus

Design outcomes

Primary

MeasureTime frameDescription
All-cause mortalityWithin 30 days of discharge from hospitalAll-cause mortality
Need for intubationAt any time during first hospitalization for hypoxia from COVID-19 up to 2 monthsNeed for intubation

Secondary

MeasureTime frameDescription
Number of repeat visits for same complaint30 daysNumber of repeat visits in 30 days for same complaint

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026