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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RECRUITING
250 participants
OBSERVATIONAL
2020-11-11
2027-02-02
Brief Summary
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Detailed Description
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I. To assess how pulmonary medicine programs adapted their procedural practices and techniques, ambulatory operations, and provider staffing in response to the coronavirus-2019 (COVID-19) epidemic.
OUTLINE:
Participants complete survey over 5-10 minutes.
Conditions
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Study Design
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CASE_ONLY
CROSS_SECTIONAL
Study Groups
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Observational (survey)
Participants complete survey over 5-10 minutes.
Survey Administration
Complete survey
Interventions
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Survey Administration
Complete survey
Eligibility Criteria
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Inclusion Criteria
* These organizations were chosen because their member databases are composed of pulmonologists in the United States (U.S.) that perform the pulmonary procedures described in this survey. Letters of approval will be obtained from these organizations and provided to the MD Anderson Institutional Review Board (IRB). Once the MD Anderson IRB approves this survey study, the survey will be sent to the relevant subcommittees of these organizations for their electronic dissemination to their membership
Exclusion Criteria
ALL
Yes
Sponsors
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M.D. Anderson Cancer Center
OTHER
Responsible Party
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Principal Investigators
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Bruce F Sabath, MD
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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Central Contacts
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Facility Contacts
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Related Links
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M D Anderson Cancer Center
Other Identifiers
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2020-0662
Identifier Type: -
Identifier Source: org_study_id
NCI-2021-01788
Identifier Type: REGISTRY
Identifier Source: secondary_id
2020-0662
Identifier Type: OTHER
Identifier Source: secondary_id
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