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The Community United to Challenge Asthma (Project CURA)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT01061424
Recruitment Status : Completed
First Posted : February 3, 2010
Last Update Posted : August 15, 2012
Sponsor:
Information provided by (Responsible Party):

Study Description
Brief Summary:
This study compares an asthma self-management intervention, delivered to the family and tailored to their needs and cultural beliefs, to standard asthma education in high-risk Puerto Rican children in elementary school. The primary outcomes are asthma medication adherence and trigger reduction.

Condition or disease Intervention/treatment
Asthma Behavioral: community health worker Behavioral: mailed information

Study Design

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 51 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Treatment
Official Title: A Community-Academic Partnership to Improve Asthma Management in Latino Children
Study Start Date : October 2009
Primary Completion Date : June 2012
Study Completion Date : June 2012

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Asthma
U.S. FDA Resources

Arms and Interventions

Arm Intervention/treatment
Active Comparator: mailed information
information on asthma is mailed to the home on the same schedule as the other arm
Behavioral: mailed information
information on asthma is mailed to the home on the same schedule as the other arm
Experimental: community health worker
community health worker provides home visits for education
Behavioral: community health worker
community health worker provides home visits for education


Outcome Measures

Primary Outcome Measures :
  1. medication adherence [ Time Frame: 1 year ]

Secondary Outcome Measures :
  1. trigger reduction [ Time Frame: 1 year ]

Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   5 Years and older   (Child, Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Puerto Rican
  • In elementary school
  • Diagnosed with asthma

Exclusion Criteria:

  • Not in school
  • Mild intermittent asthma
  • Well controlled asthma
Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01061424


Locations
United States, Illinois
Rush University Medical Center
Chicago, Illinois, United States, 60612
Sponsors and Collaborators
Rush University Medical Center
Investigators
Principal Investigator: Molly A Martin, MD Rush University Medical Center
More Information

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Molly A. Martin, MD, MD, Rush University Medical Center
ClinicalTrials.gov Identifier: NCT01061424     History of Changes
Other Study ID Numbers: 1R21HL087769-01A1 ( U.S. NIH Grant/Contract )
First Posted: February 3, 2010    Key Record Dates
Last Update Posted: August 15, 2012
Last Verified: August 2012

Keywords provided by Molly A. Martin, MD, Rush University Medical Center:
pediatric asthma

Additional relevant MeSH terms:
Asthma
Bronchial Diseases
Respiratory Tract Diseases
Lung Diseases, Obstructive
Lung Diseases
Respiratory Hypersensitivity
Hypersensitivity, Immediate
Hypersensitivity
Immune System Diseases