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Rehabilitation-focused program for COVID-19 (LAUREL Trial)
N/A
Recruiting
Led By Kristina A Crothers, MD
Research Sponsored by VA Office of Research and Development
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up change in score from 3-8 weeks (after diagnosis or discharge to home) to months 6 and 12
Awards & highlights
LAUREL Trial Summary
This trial will study the effects of COVID-19 and how to help patients recover through rehabilitation programs.
Eligible Conditions
- COVID-19
- Coronavirus
- Lung Disease
LAUREL Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ change in score from 3-8 weeks (after diagnosis or discharge to home) to months 6 and 12
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~change in score from 3-8 weeks (after diagnosis or discharge to home) to months 6 and 12
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
EuroQol 5 Dimension 5 Level (EQ-5D-5L) overall utility index
EuroQol 5 Dimension 5 Level (EQ-5D-5L) visual analog score
WHO Disability Assessment Schedule 2.0 (WHODAS 2.0)
LAUREL Trial Design
1Treatment groups
Experimental Treatment
Group I: Rehabilitation-focused programExperimental Treatment1 Intervention
Subjects will receive multiple services in a rehabilitation-focused program
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Who is running the clinical trial?
VA Office of Research and DevelopmentLead Sponsor
1,609 Previous Clinical Trials
3,305,957 Total Patients Enrolled
15 Trials studying COVID-19
412,748 Patients Enrolled for COVID-19
Kristina A Crothers, MDPrincipal InvestigatorVA Puget Sound Health Care System Seattle Division, Seattle, WA
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