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Active Not RecruitingNCT04447222

Impact of the COVID-19 Pandemic and HRQOL in Cancer Patients and Survivors

COVID-19: Well-Being and HRQOL in Cancer Patients Who Participated in Prior Behavioral Clinical Trials

Status
Active Not Recruiting
Phase
Study type
Observational
Enrollment
1,242 (estimated)
Sponsor
M.D. Anderson Cancer Center · Academic / Other
Sex
All
Age
Healthy volunteers
Accepted

Summary

This study uses questionnaires to gain an understanding of how experiences during the COVID-19 pandemic, regardless of COVID-19 status, may have impacted health-related quality of life (HRQOL) and other areas such as COVID-19-specific psychological distress, disruptions to health care, finances and social interactions in cancer patients. The coronavirus disease 2019 (COVID-19) is an infectious disease that is caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The information learned from this study will guide the development of psychosocial programs to improve patient care and outcomes in cancer patients and survivors in the context of facing a global pandemic.

Detailed description

PRIMARY OBJECTIVES: I. Assess experiences during the coronavirus disease-2019 (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 HRQoL and other psychosocial and behavioral factors in cancer survivors who participated in one of three prior clinical trials. 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 assessed concurrently and other psychosocial measures assessed in the prior trials moderate the effects of COVID-19 experiences on COVID-19-specific psychological distress and HRQoL. IV. Examine group differences in the outcomes assessed in the protocol relative to prior group assignment in the behavioral clinical trials. OUTLINE: Participants complete a survey online over 35-45 minutes about their experiences regarding the COVID-19 pandemic.

Conditions

Interventions

TypeNameDescription
OTHERQuality-of-Life AssessmentAncillary studies
OTHERQuestionnaire AdministrationAncillary studies
OTHERSurvey AdministrationComplete survey

Timeline

Start date
2020-05-12
Primary completion
2026-07-30
Completion
2026-07-30
First posted
2020-06-25
Last updated
2026-02-19

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04447222. Inclusion in this directory is not an endorsement.