Status:
COMPLETED
Burnout and Distress preventiOn With caNnabidiol in Front-line Health Care workerS deAling wIth COVID-19
Lead Sponsor:
University of Sao Paulo
Conditions:
Covid19
Burn Out
Eligibility:
All Genders
24-60 years
Phase:
PHASE2
PHASE3
Brief Summary
The objective of this work is to monitor the level of stress and overload of a group of front-line health workers (physicians, nurses and physiotherapists) who will participate in the care of patients...
Detailed Description
The Bonsai study is a two-arm, parallel-group, individually randomized (1:1 allocation ratio), controlled with general measures (supporting motivational videos, fitness videos), participant and invest...
Eligibility Criteria
Inclusion
- age between 24 and 60 years old
- Research participants of both sexes.
- HCFMRP physicians, nurses and physiotherapists involved in the care of patients who have undergone screening and present at least one symptom, which may be related to infection by COVID-19.
- Good health conditions and without conditions that characterize them as belonging to the risk groups associated with COVID infection19.
- Research participants with the potential to become pregnant may be included in the study as long as they are sexually abstinent or using a contraceptive method considered effective.
- Signature of the Free and Informed Consent Term approved (ICF) by the Research Ethics Committee (CEP) and CONEP.
Exclusion
- Using any medication with potential interaction with CBD or with a history of undesirable reactions prior to the use of this cannabinoid.
- Physicians, nurses and physiotherapists with occasional contact with patients with COVID-19 and who are not responsible for the continuous monitoring of these patients.
- Although in the HC-FMRP-USP care allocation policy, professionals who are eventually more susceptible to complications from the new coronavirus will be relocated to not attend patients with COVID19, it will be checked again to exclude patients with chronic diseases: diabetes, hypertension, lung disease like asthma or COPD; hematological diseases, chronic kidney disease and immunodepression.
- Professionals over 60 years old
- Female research participants who become pregnant or male participants who have their pregnant partner during the research project
Key Trial Info
Start Date :
June 16 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 16 2020
Estimated Enrollment :
120 Patients enrolled
Trial Details
Trial ID
NCT04504877
Start Date
June 16 2020
End Date
December 16 2020
Last Update
September 28 2021
Active Locations (1)
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1
Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto - USP
Ribeirão Preto, São Paulo, Brazil, 14048-900