Copeptin and Psychological Stress of Medic During COVID-19 Pandemic

Alexandria University

Status: Completed

Conditions: Psychological Stress; Hemostatic Disorder

Study type: Observational

Funder types: Other

Identifiers

NCT04757285

0304842

Details and patient eligibility

About

Psychological stress (PSS) is one of the most common problems among healthcare providers during COVID-19 pandemic. PSS influences the homeostatic equilibrium of the body, involving activation of the sympathetic nervous system and hypothalamus pituitary adrenal (HPA) axis. Copeptin; C-terminal portion of Vasopressin (AVP) precursor is stable. Nevertheless, Evidence about influence of PSS on copeptin levels is lacking. The reason we are doing this research is to determine the level of psychological stress among healthcare providers exposed to at the time of work in intensive care unit (ICU) during COVID-19 pandemic; They will be appraised every assembly for psychological stress level; before start of duty shifts (first time), one week after start (second time) and two weeks after departure from shift duties in ICU (third time) for assessment of psychological stress level and stress hormones.

Full description

A total of 70 healthcare personnel volunteers participated; 35 physicians and 35 nurses. All healthcare providers' volunteers are in good physical health, Exclusion criteria included hypertension, diabetes mellitus, obesity BMI ≥30, subjects with serum sodium ≤135 or ≥ 145 mmol /L at baseline or females receiving contraceptive pills.

During the research participants will answer a questionnaire as well as three blood samples are taken.

• In the first meeting, evaluation of participant general condition; determining BMI, blood pressure. Then a small amount of blood, equal to about two millimeters, will be taken from participant arm with a syringe. This blood will be tested for serum copeptin, cortisol (fasting morning sample). The investigator will ask participant few questions to evaluate the level of stress (as anxiety, insomnia, fear of infection through questionnaire)
• The second meeting, one week after work in ICU, another blood sample will be taken from participant and determine level of psychological stress.
• The third meeting, two weeks after leave from ICU participant blood sample will be taken from participant to determine stress hormones and determine level of psychological stress.

Duration

The research takes place over six months in total.

Enrollment: 90 patients

Sex: All

Ages: 24 to 37 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

physicians and nurses under age of 37 years in good health

Exclusion criteria

• body mass index above 30
• hypertension
• Diabetes mellitus
• females receiving contraceptive pills

Trial design

90 participants in 2 patient groups

control group

Description:

25 healthcare personnel volunteers not working in quarantine hospitals of matched age

healthcare providers worked in Intensive Care Units

Description:

35 physicians (28 males and 7 females) and 35 nurses (10 males and 25 females). All volunteers were in good physical health Exclusion criteria included hypertension, diabetes mellitus, obesity BMI ≥30, subjects with serum sodium ≤135 or ≥ 145 mmol /L at baseline or females receiving contraceptive pills. Assigned participants were clinically evaluated for as hypertension, DM, dyslipidemia, renal function.