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Impact of reinforced awake proning on outcomes of COVID-19 pnemonia

: A cluster randomized trial of a behaviour change intervention to better implement awake PROning manoeuvRE in COVID-19 patiEnts: ( PRO- RECOVER RCT) - PRO- RECOVER RCT

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/06/034340
Enrollment
302
Registered
2021-06-22
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: B972- Coronavirus as the cause of diseases classified elsewhere Health Condition 2: J128- Other viral pneumonia

Interventions

Intervention1: MULTI-COMPONENT,EDUCATIONAL INTERVENTION TO INDUCE BEHAVIOUR CHANGE: EDUCATIONAL VIDEO, and leaflets that emphasise the importance of proning and ,TRACKERS TO RECORD TIME SPENT IN PRON

Sponsors

NONE
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: CONSENTING COVID 19 PATIENTS HOSPITALISED FOR MILD,MODERATE,SEVERE DISEASE

Exclusion criteria

Exclusion criteria: 1. Inability to prone due to mechanical reasons 2. Heart failure NYHA Class 3/4 3. Decompensated Chronic Liver Disease with ascites 4. Presence of Pneumothorax or Pneumomediastinum 5. Critically Ill patients 6. Intubated patients 7. Morbid obesity 8. Pregnancy 9. Unstable Fractures 10. Acute Hypercapnic respiratory failure 11. Deep Vein Thrombosis (untreated 12. Other contraindications to Prone position documented in the Case record by the treating physician. 13. Intervention delayed beyond 48 hours of admission.

Design outcomes

Primary

MeasureTime frame
Need for invasive or non invasive ventilation or the occurence of death.Timepoint: At baseline, then daily till 7 days in both arms. After this all patients will be followed up till discharge or death. Final outcome will be recorded at that time.

Secondary

MeasureTime frame
Resolution of hypoxia and the need for escalation of care.Timepoint: At baseline, and then daily for 7 days. Secondary outcomes will be finally recorded at discharge or death

Countries

India

Contacts

Public ContactSoumya Umesh

ST JOHNS MEDICAL COLLEGE AND HOSITAL

drsoumya239@gmail.com08022065834

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026