Well-Being and Health-Related Quality of Life in Melanoma Patients During COVID-19 Pandemic
- Conditions
- COVID-19 InfectionMelanoma
- Interventions
- Other: Survey Administration
- Registration Number
- NCT04474301
- Lead Sponsor
- M.D. Anderson Cancer Center
- Brief Summary
The primary purpose of this study is to gain an understanding of how experiences during the COVID-19 pandemic, regardless of COVID-19 status, may have impacted multiple domains of health-related quality of life and other areas such as COVID-19 specific psychological distress, and disruptions to health care, finances and social interactions. We will also evaluate the extent to which resiliency factors such as social support, perceived benefits under times of stress, and ability to manage stress may buffer associations between COVID-19 experiences and HRQoL. To meet these objectives, we have developed a 10-minute questionnaire that taps into these areas and is based on prior work addressing concerns of other pandemics or national crises. Participants will have previously consented to protocol PA15-0336 and have provided prior lifestyle data. This will allow us to connect the COVID-19 survey data with prior existing data.
- Detailed Description
PRIMARY OBJECTIVES:
I. Assess experiences during the COVID-19 pandemic (e.g., exposure, risk factors, testing, isolation, seropositivity, hospitalization, loss of family or friends); COVID-19-specific psychological distress (e.g., fear, anxiety and depressive symptoms); health, financial and social disruptions; perceived benefits and social support; and health-related quality of life (HRQoL) in melanoma patients who participated in protocol PA15-0336.
II. Evaluate the extent to which COVID-19 experiences are associated with COVID-19-specific psychological distress, health, financial and social disruptions, perceived benefits and social support, and HRQoL.
III. Evaluate the extent to which resiliency factors such as social support and perceived benefits moderate the effects of COVID-19 experiences on COVID-19-specific psychological distress and HRQoL.
IV. Explore the association between prior lifestyle data collected as part of PA15-0336 and COVID-19-specific psychological distress and HRQoL.
OUTLINE:
Patients complete a survey over 10 minutes.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 1152
- Patients who have signed consent for PA15-0336
- Has an active email address and can be contacted via MyChart
- Documentation of being alive per the cancer registry
Not provided
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Observational (survey administration) Survey Administration Patients complete a survey over 10 minutes.
- Primary Outcome Measures
Name Time Method COVID-19-specific health Survey completion Up to 2 months Prior lifestyle data Survey completion Up to 2 months Will explore the association between prior lifestyle data collected as part of PA15-0336 and COVID-19-specific psychological distress and HRQoL.
COVID-19-specific health related quality of life (HRQoL) Survey completion Up to 2 months Experiences during the COVID-19 pandemic Survey completion Up to 2 months Including exposure, risk factors, testing, isolation, seropositivity, hospitalization, or loss of family or friends.
Effects of COVID-19 experiences on COVID-19-specific psychological distress and HRQoL Survey completion Up to 2 months Will evaluate the extent to which resiliency factors such as social support and perceived benefits moderate the effects of COVID-19 experiences on COVID-19-specific psychological distress and HRQoL.
COVID-19-specific psychological distress Survey completion Up to 2 months COVID-19-specific financial and social disruptions Survey completion Up to 2 months COVID-19-specific perceived benefits and social support Survey completion Up to 2 months
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
M D Anderson Cancer Center
🇺🇸Houston, Texas, United States