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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04631380
Other study ID # PRAYER-COVID19
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 1, 2020
Est. completion date January 1, 2022

Study information

Verified date March 2022
Source Hospital do Coracao
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 200
Est. completion date January 1, 2022
Est. primary completion date June 1, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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


Related Conditions & MeSH terms


Intervention

Other:
PRAYER
THE PRAYER GROUP WILL RECEIVE ABSOLUTELY THE SAME CARE AS THE CONTROL GROUP PLUS PRAYERS

Locations

Country Name City State
Brazil Hospital do Coracao Sao Paulo SP

Sponsors (1)

Lead Sponsor Collaborator
Hospital do Coracao

Country where clinical trial is conducted

Brazil, 

References & Publications (5)

Bleich A. [Intercessory prayer for health: a matter of faith, science or both]. Harefuah. 2002 Jun;141(6):522-3. Hebrew. — View Citation

Harris WS, Gowda M, Kolb JW, Strychacz CP, Vacek JL, Jones PG, Forker A, O'Keefe JH, McCallister BD. A randomized, controlled trial of the effects of remote, intercessory prayer on outcomes in patients admitted to the coronary care unit. Arch Intern Med. 1999 Oct 25;159(19):2273-8. Erratum in: Arch Intern Med 2000 Jun 26;160(12):1878. — View Citation

Hettiaratchy S, Hemsley C. Effect of retroactive intercessory prayer. Paper proves power of statistics, not prayer. BMJ. 2002 Apr 27;324(7344):1037; author reply 1038-9. — View Citation

Hoover DR, Margolick JB. Questions on the design and findings of a randomized, controlled trial of the effects of remote, intercessory prayer on outcomes in patients admitted to the coronary care unit. Arch Intern Med. 2000 Jun 26;160(12):1875-6; author reply 1877-8. — View Citation

Radin D, Schlitz M, Baur C. Distant Healing Intention Therapies: An Overview of the Scientific Evidence. Glob Adv Health Med. 2015 Nov;4(Suppl):67-71. doi: 10.7453/gahmj.2015.012.suppl. Epub 2015 Nov 1. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary DEATH OR RECOVERY WE WILL EVALUATE DEATHS OR HOSPITAL DISCHARGE 60 DAYS
Secondary NEED FOR MECHANICAL VENTILATION NEED FOR MECHANICAL VENTILATION 60 DAYS
Secondary TIME OF REMAINED INTUBATED TIME OF REMAINED INTUBATED 60 DAYS
Secondary LENGTH OF STAY IN ICU LENGTH OF STAY IN ICU 60 DAYS
Secondary TIME OF STAY HOSPITALIZED TIME OF STAY HOSPITALIZED 60 DAYS
Secondary Occurrence of clinical complications. Occurrence of clinical complications that were not included before diagnostic confirmation and that may be related to covid infection. 60 DAYS
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