Well-being in Cancer Patients With Neuropathy During COVID-19 Who Participated in Prior Clinical Trials
NCT ID: NCT04650178
Last Updated: 2025-10-14
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
274 participants
OBSERVATIONAL
2020-05-26
2027-04-30
Brief Summary
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Detailed Description
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I. Assess experiences during the coronavirus disease 2019 (COVID-19) pandemic of the health-related quality of life (HRQOL) (e.g. physical, emotional, social well-being), and other COVID-19-specific domains (e.g. anxiety, social interactions, finances), and the associations between COVID-19 experiences and COVID-19-specific distress, HRQOL and clinical outcomes of patients who participated in one of three clinical trials.
II. Examine differences in outcomes between neuropathic pain patients who participated in one of two trials of NFB and received NFB, and neuropathic pain patients who participated in a non-treatment-related neuropathy study (i.e., who did not receive NFB).
III. Evaluate the extent to which coping and resilience factors moderate the effects of COVID-19 experiences on COVID-19-specific distress, HRQOL and clinical outcomes.
OUTLINE:
Patients complete an online questionnaire over 15 minutes about their experiences regarding the COVID-19 pandemic including testing, risks of exposure, whether people they know have acquired COVID-19, as well as questions on how the pandemic has impacted their quality of life.
Conditions
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Study Design
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COHORT
OTHER
Study Groups
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Observational (questionnaire, quality of life)
Patients complete an online questionnaire over 15 minutes about their experiences regarding the COVID-19 pandemic including testing, risks of exposure, whether people they know have acquired COVID-19, as well as questions on how the pandemic has impacted their quality of life.
Quality-of-Life Assessment
Ancillary studies
Questionnaire Administration
Complete questionnaire
Interventions
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Quality-of-Life Assessment
Ancillary studies
Questionnaire Administration
Complete questionnaire
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Has an active email address or can be contacted by MyChart or personal email
Exclusion Criteria
ALL
No
Sponsors
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National Cancer Institute (NCI)
NIH
M.D. Anderson Cancer Center
OTHER
Responsible Party
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Principal Investigators
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Sarah Prinsloo
Role: PRINCIPAL_INVESTIGATOR
M.D. Anderson Cancer Center
Locations
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M D Anderson Cancer Center
Houston, Texas, United States
Countries
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Related Links
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MD Anderson Cancer Center Website
Other Identifiers
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NCI-2020-06014
Identifier Type: REGISTRY
Identifier Source: secondary_id
2020-0508
Identifier Type: OTHER
Identifier Source: secondary_id
2020-0508
Identifier Type: -
Identifier Source: org_study_id
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