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Improving Asthma Care Through Parental Empowerment (PEPAC)
This study is currently recruiting participants.
Verified by Children's Research Institute, January 2009
First Received: January 29, 2009   Last Updated: August 4, 2009   History of Changes
Sponsored by: Children's Research Institute
Information provided by: Children's Research Institute
ClinicalTrials.gov Identifier: NCT00832923
  Purpose

The overall aim of this study will be to perform a prospective randomized clinical trial of an enhanced version of the IMPACT DC intervention involving short-term case management to facilitate PCP follow-up appointments and to provide education for parents about how to communicate more effectively with their children's PCPs as a means

(1) to improve the rate of utilization of primary care services for ongoing asthma care and (2) to enhance the self-efficacy of parents in their interactions with their children's provider regarding the child's asthma care needs in 150 parents of high risk children referred within the IMPACT DC Asthma Clinic.


Condition Intervention
Asthma
Behavioral: PEPAC

Study Type: Interventional
Study Design: Health Services Research, Randomized, Single Blind (Caregiver), Parallel Assignment
Official Title: Improving Asthma Care Through Parental Empowerment: Effect on Healthcare Utilization and Parent Self-Efficacy

Resource links provided by NLM:


Further study details as provided by Children's Research Institute:

Primary Outcome Measures:
  • Utilization of Primary Care Provider [ Time Frame: 2 months & 6 months after visit ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Parental Self-efficacy in communicating about Asthma care with child's primary care provider [ Time Frame: 2 months & 6 months after visit ] [ Designated as safety issue: No ]

Estimated Enrollment: 150
Study Start Date: January 2009
Estimated Primary Completion Date: July 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Routine IMPACT DC care: No Intervention
Participants receive standard asthma education as routine for IMPACT DC
Enhanced care PEPAC Intervention: Experimental Behavioral: PEPAC
The proposed enhancement of the IMPACT DC intervention will consist of three key components: (1) an enhanced IMPACT DC Asthma Clinic visit; (2) short-term case management to increase the rate of primary care follow-up visits in the first month after the IMPACT DC Asthma Clinic visit; and (3) training in an "asthma care toolkit" to improve communication around asthma care with the child's primary care provider.

Detailed Description:

Asthma is the most common chronic disease of childhood, and it disproportionately affects urban, minority, and disadvantaged children. When implemented correctly, existing evidence-based guidelines from the National Heart, Lung, and Blood Institute (NHLBI) improve pediatric asthma care and outcomes. One key component of these guidelines is the importance of longitudinal care as part of a partnership among patient, parents, and a healthcare provider. Such a partnership depends on effective communication of healthcare status by parents to providers. Improving the communication skills of inner-city parents may improve their ability to obtain more effective longitudinal asthma care within their primary care homes and thereby to improve their child's asthma health outcomes. IMPACT DC ("Improving Pediatric Asthma Care in the District of Columbia") is a locally validated emergency department (ED) based intervention that improves multiple measures of asthma care and outcomes through an intensive short-term program of asthma education, medical care, and care coordination. In spite of these successes, achieving increased subsequent contact and partnership with primary care providers (PCPs) for asthma care after the intervention has not been successful. Therefore, for the current study, we propose to assess the effectiveness of an enhanced version of the existing IMPACT DC intervention consisting of short-term case management by trained asthma educators.

  Eligibility

Ages Eligible for Study:   12 Months to 12 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • ages between 12 months and 12 years, inclusive
  • prior physician diagnosed asthma
  • ability of the parent to identify a specific PCP for their child
  • public insurance covering the child
  • parent/guardian available for interview

Exclusion Criteria:

  • significant medical co-morbidities
  • enrollment in another asthma research intervention study
  • unavailability for telephone follow-up
  • primary language of the caregiver other than English
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00832923

Contacts
Contact: Kanya Shabazz 202-476-6266 kshabazz@cnmc.org
Contact: Debbie Quint, MPH 202-476-5514 dquint@cnmc.org

Locations
United States, District of Columbia
Children's Research Institute Recruiting
Washington, District of Columbia, United States, 20010
Contact: Kanya Shabazz     202-476-6266     kshabazz@cnmc.org    
Principal Investigator: Ivor B Horn, MD, MPH            
Sub-Investigator: Stephen J Teach, MD, MPH            
Sub-Investigator: Jill G Joseph, MD. PhD            
Sponsors and Collaborators
Children's Research Institute
  More Information

No publications provided

Responsible Party: Children's Research Institute ( Ivor B. Horn, MD, MPH )
Study ID Numbers: RAC #207
Study First Received: January 29, 2009
Last Updated: August 4, 2009
ClinicalTrials.gov Identifier: NCT00832923     History of Changes
Health Authority: United States: Institutional Review Board

Keywords provided by Children's Research Institute:
parental empowerment
parent self-efficacy

Study placed in the following topic categories:
Hypersensitivity
Lung Diseases, Obstructive
Respiratory Tract Diseases
Bronchial Diseases
Lung Diseases
Hypersensitivity, Immediate
Asthma
Respiratory Hypersensitivity

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

ClinicalTrials.gov processed this record on August 28, 2009