Purpose

This study investigates the impact of the COVID-19 pandemic on the psychosocial health of employees of MD Anderson Cancer Center. Epidemics have been shown to promote psychological stress among medical staff in high risk areas, which may lead to mental health problems. Assessing how the pandemic is affecting employees may allow for more comprehensive actions to be taken to protect the mental health of employees.

Condition

Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Criteria

Inclusion Criteria:

- MD Anderson employees

Study Design

Phase
Study Type
Observational
Observational Model
Cohort
Time Perspective
Cross-Sectional

Arm Groups

ArmDescriptionAssigned Intervention
Observational (questionnaire) Participants complete 2 online questionnaires over 10 minutes each at baseline and at 3 months after the pandemic ends.
  • Other: Questionnaire Administration
    Complete questionnaires

Recruiting Locations

M D Anderson Cancer Center
Houston, Texas 77030
Contact:
Priya R. Bhosale
713-792-0221
priya.bhosale@mdanderson.org

More Details

NCT ID
NCT04491292
Status
Recruiting
Sponsor
M.D. Anderson Cancer Center

Study Contact

Priya R. Bhosale
713-792-0221
priya.bhosale@mdanderson.org

Detailed Description

PRIMARY OBJECTIVE: I. To assess psychosocial and stress-related outcomes in employees at MD Anderson Cancer Center during and post the COVID-19 pandemic. SECONDARY OBJECTIVE: I. To identify demographic and occupational factors associated with COVID-19 related psychosocial and stress outcomes. OUTLINE: Participants complete 2 online questionnaires over 10 minutes each at baseline and at 3 months after the pandemic ends.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.