Prayer in Commbate to Corona Virus - Covid -19

Not Applicable

Completed

• Conditions: Covid19

• Registration Number: NCT04631380
• Lead Sponsor: Hospital do Coracao

Brief Summary

PATIENTS WHO ARE ADMITTED TO HOSPITALIZATION IN HCOR AND WHO HAVE THE CONFIRMED DIAGNOSIS OF CORONA VIRUS, WILL BE ASKED TO CONSENT TO PARTICIPATE IN THIS STUDY THAT INTENDS TO STUDY THE EFFECTIVENESS OF THE REMOTE INTERCESSION PRAYER IN COMBATING THIS DISEASE.

Detailed Description

PATIENTS WHO AGREE TO PARTICIPATE IN THE STUDY WILL BE SEPARATED INTO 2 GROUPS, THE INTERVENTION GROUP AND THE CONTROL GROUP.

THE IDENTITY OF THE PATIENTS WILL BE KEPT IN SECRET AND ONLY THEIR INITIALS WILL BE LISTED.

THE INTERVENTION GROUP WILL RECEIVE DAILY PRAYERS AND THE EVOLUTIONARY CLINICAL RESULTS OF THE TWO GROUPS WILL BE PURCHASED.

Study Timeline

• Study Start: 2020-08-01
• Study First Submitted: 2020-08-04
• Study First Submitted QC: 2020-11-13
• Study First Posted: 2020-11-17
• Primary Completion: 2021-06-01
• Study Completion: 2022-01-01
• Status Verified: 2022-03
• Last Update Submitted: 2022-03-16
• Last Update Posted: 2022-03-17

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 200

Inclusion Criteria

Patients hospitalized in comun hospital rooms and intensive care units with confirmed COVID-19.

Exclusion Criteria

• Patients admitted to the HCor emergency room, diagnosed with COVID-19 infection, however, without indication for hospitalization
• Patients admitted to the HCor emergency room, diagnosed with COVID-19 infection, however, without indication for hospitalization.
• Patients 18 years of age or older
• Patients with indication of palliative care and definition of terminality at hospital admission
• Patients who voluntarily choose not to participate in the study at the time of the • presentation of the Informed Consent Form.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
DEATH OR RECOVERY	60 DAYS	WE WILL EVALUATE DEATHS OR HOSPITAL DISCHARGE

Secondary Outcome Measures

Name	Time	Method
TIME OF REMAINED INTUBATED	60 DAYS	TIME OF REMAINED INTUBATED
LENGTH OF STAY IN ICU	60 DAYS	LENGTH OF STAY IN ICU
TIME OF STAY HOSPITALIZED	60 DAYS	TIME OF STAY HOSPITALIZED
NEED FOR MECHANICAL VENTILATION	60 DAYS	NEED FOR MECHANICAL VENTILATION
Occurrence of clinical complications.	60 DAYS	Occurrence of clinical complications that were not included before diagnostic confirmation and that may be related to covid infection.

Trial Locations

Locations (1)

Hospital do Coracao; 🇧🇷 Sao Paulo, SP, Brazil