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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04402801
Other study ID # 22327
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 1, 2020
Est. completion date May 31, 2022

Study information

Verified date November 2023
Source University of Virginia
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Adult patients with Cystic Fibrosis who are seen at the specialty CF clinic at University of Virginia will be given an option to utilize telemedicine instead of in-person visits for standard clinic visits. Health information from standard of care visits including FEV1, exacerbations, leading to oral or intravenous antibiotics, laboratory results, hospitalization records, and responses to health questionnaires will be recorded for research purposes. Data collected for the research study will be compared to baseline and previous years to determine if there are any deleterious effects for those who transition to telemedicine clinic visits.


Recruitment information / eligibility

Status Completed
Enrollment 140
Est. completion date May 31, 2022
Est. primary completion date May 31, 2022
Accepts healthy volunteers
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - Adult patients (18-year-old and older) with CF seen in the UVA adult CF clinic who agree to participate in the study. Exclusion Criteria: - Patients who cannot consent to the research study. In addition, prisoners will not be included.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States University of Virginia Health System Charlottesville Virginia

Sponsors (1)

Lead Sponsor Collaborator
University of Virginia

Country where clinical trial is conducted

United States, 

References & Publications (1)

Somerville LAL, List RP, Compton MH, Bruschwein HM, Jennings D, Jones MK, Murray RK, Starheim ER, Webb KM, Gettle LS, Albon DP. Real-World Outcomes in Cystic Fibrosis Telemedicine Clinical Care in a Time of a Global Pandemic. Chest. 2022 May;161(5):1167-1 — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary FEV1 stability A change of 10% or more in FEV1 percent predicted will be considered significant; FEV1 pre and pos covid telemedicine implementation will be compared 12 months
Secondary Exacerbation rate Exacerbation rate pre and pos covid telemedicine implementation will be compared 12 months
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