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Effect of Prone Positioning in Patients With COVID-19

Effect of Prone Positioning and Alternate Nostril Breathing Technique in Patients With COVID-19: A Quasi Experimental Study.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04710771
Enrollment
30
Registered
2021-01-15
Start date
2020-11-23
Completion date
2021-01-29
Last updated
2025-05-15

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

Conditions

Covid19

Keywords

Covid-19, General Anxiety Disorder-7, Prone Position, Alternate Nostril Breathing

Brief summary

COVID-19 is affecting the people around the world and the infected individuals' may either stay asymptomatic or present to hospitals with severe distress and life threatening symptoms. The objective of the study is to investigate role of Prone positioning and alternate nostril breathing in patients with Covid-19.

Detailed description

In this quasi experimental study, 30 patients aged 40-80 years of either gender with a confirmed diagnosis of COVID-19 receiving supplemental oxygen were recruited from DHQ Hospital Faisalabad. patients were grouped into two A & B. We collected baseline data on demographics and anthropometrics. After baseline data collection, all the patients were helped into the prone position, which was maintained for a minimum duration of three hours. After that patients in group B performed alternate nostril breathing for 10 minutes with help of physiotherapist. Clinical data were re-collected on 3rd day of intervention one hour after returning to the supine position in group A and after alternate nostril breathing in group B. The main study outcome was the variation in oxygenation (partial pressure of oxygen \[PaO2\]/ fractional concentration of oxygen in inspired air \[FiO2\]) between baseline and resupination, and General psychological state through GAD-7 General anxiety disorder questionnaire.

Interventions

OTHERProne Lying Position

patient lies on his/ her stomach facing floor.

patient inspires with one nostril at a time, right or left one by one and expires by mouth.

Sponsors

Sialkott College of Physical Therapy
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

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

Inclusion criteria

Age: 40-80 Gender: Both GCS score:15

Exclusion criteria

* COPD Intubated ARDS Smoker Neurological Disorder

Design outcomes

Primary

MeasureTime frameDescription
PaO2Change in score before the intervention on 1st day of intervention and on 3rd day one hour after the intervention.partial pressure of oxygen.
FiO2Change in score before the intervention on 1st day of intervention and on 3rd day one hour after the intervention.Fractional concentration of oxygen in inspired air \[FiO2\])
General Anxiety Disorder-7 ScoreChange in score before the intervention on 1st day of intervention and on 3rd day one hour after the intervention.general anxiety disorder-7 score ranges from 0-21, out of which 0-4 means minimal anxiety, 5-9 stands for mild anxiety, 10-14 for moderate and 15-21 for severe anxiety.

Countries

Pakistan

Outcome results

None listed

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