Actively Recruiting
Psychosocial Impact of COVID-19 Pandemic on MD Anderson Workforce
Led by M.D. Anderson Cancer Center · Updated on 2026-01-28
20000
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
M
M.D. Anderson Cancer Center
Lead Sponsor
N
National Cancer Institute (NCI)
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research aims to understand how the COVID-19 pandemic affects the mental and emotional well-being of employees at MD Anderson Cancer Center. It focuses on measuring psychosocial stress and related outcomes during and after the pandemic to identify factors influencing these effects among medical staff in a high-risk environment. Participants are asked to complete two online questionnaires, each taking about 10 minutes. These surveys are done once at the start of the study and again three months after the pandemic ends to capture changes over time in stress and psychosocial health. During the study, researchers will analyze the questionnaire responses to track changes in psychosocial and stress-related outcomes from baseline through three months after the pandemic. They will also explore how demographic and job-related factors relate to these outcomes. Participation involves minimal time commitment and is fully conducted online, with no additional procedures or visits.
CONDITIONS
Brief Title
Assessment of the Psychosocial Impact of the COVID-19 Pandemic on the MD Anderson Cancer Center Workforce
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Currently employed by MD Anderson Cancer Center
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 online screening questionnaire
Duration - Up to 3 months after the pandemic ends
Participants complete questionnaires to assess psychosocial and stress-related outcomes during and after the COVID-19 pandemic.
2 online questionnaires: one at baseline and one at 3 months after the pandemic ends
Trial Site Locations
Total: 1 location
1
M D Anderson Cancer Center
Houston, Texas, United States, 77030
Actively Recruiting
Research Team
P
Priya R. Bhosale
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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