The Impact of COVID-19 on Pulmonary Procedures

NCT ID: NCT05022446

Last Updated: 2026-02-13

Study Results

Results pending

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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Recruitment Status

RECRUITING

Total Enrollment

250 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-11-11

Study Completion Date

2027-02-02

Brief Summary

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This study investigates the changes in practice by pulmonary procedural programs across the United States as they faced the coronavirus pandemic. Information gathered from this study may help guide pulmonary programs on a wider scale and improve their practice. The study may also help researchers understand where they should focus research efforts to better respond to a pandemic in the future.

Detailed Description

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PRIMARY OBJECTIVE:

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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COVID-19 Infection Hematopoietic and Lymphoid Cell Neoplasm Malignant Solid Neoplasm

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Observational (survey)

Participants complete survey over 5-10 minutes.

Survey Administration

Intervention Type OTHER

Complete survey

Interventions

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Survey Administration

Complete survey

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Pulmonologists that are members of the American Association of Bronchology and Interventional Pulmonology (AABIP) and/or the American College of Chest Physicians (ACCP)
* 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

None
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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M.D. Anderson Cancer Center

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

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

Site Status RECRUITING

Countries

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United States

Central Contacts

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Jhankruti F Zaveri, MPH

Role: CONTACT

(713) 745-2645

Facility Contacts

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Bruce F. Sabath

Role: primary

240-476-8938

Related Links

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http://www.mdanderson.org

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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