RECRUITING

Patient Reported Outcomes for Acute Asthma Care Treatment

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Asthma affects 1 in every 12 persons in the U.S., resulting in 1.9 million ED visits annually; however, the impact of ED care on patient-reported outcomes after acute exacerbations is unknown. The proposed research will train a physician-scientist to develop a novel instrument to assess patient-reported outcomes after adult ED asthma visits, evaluate the association between ED clinical processes and patient-reported outcomes, and test the association between patient-reported outcomes and subsequent acute care utilization. The candidate will acquire skills in patient-centered research, instrument development and validation, and risk adjusted outcome measurement that will enable her transition to independence.

Official Title

Patient Reported Outcomes for Acute Asthma Care Treatment

Quick Facts

Study Start:2019-09-24
Study Completion:2024-07-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04349020

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Age 18 or older
  2. * English-speaking
  3. * Prior diagnosis of asthma per the electronic health record
  4. * Experiencing an ED visit for asthma as per ED clinician
  5. * Medically appropriate for survey study as determined by treating ED clinician
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Michelle Lin, MD, MPH, MS
CONTACT
212-824-8067
Michelle.Lin@mountsinai.org
Lauren Gordon, MPH
CONTACT
212-824-8037
lauren.gordon@mountsinai.org

Principal Investigator

Michelle Lin, MD, MPH, MS
PRINCIPAL_INVESTIGATOR
Icahn School of Medicine at Mount Sinai

Study Locations (Sites)

Mount Sinai Beth Israel
New York, New York, 10003
United States
Icahn School of Medicine at Mount Sinai
New York, New York, 10029
United States

Collaborators and Investigators

Sponsor: Stanford University

  • Michelle Lin, MD, MPH, MS, PRINCIPAL_INVESTIGATOR, Icahn School of Medicine at Mount Sinai

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2019-09-24
Study Completion Date2024-07-31

Study Record Updates

Study Start Date2019-09-24
Study Completion Date2024-07-31

Terms related to this study

Keywords Provided by Researchers

  • Patient Reported Outcomes

Additional Relevant MeSH Terms

  • Asthma