Asthma symptom perception feedback intervention for ethnic minority adolescents

Information

  • Research Project
  • 9051139
  • ApplicationId
    9051139
  • Core Project Number
    R01HL128260
  • Full Project Number
    1R01HL128260-01A1
  • Serial Number
    128260
  • FOA Number
    PA-13-302
  • Sub Project Id
  • Project Start Date
    12/15/2015 - 9 years ago
  • Project End Date
    12/16/2015 - 9 years ago
  • Program Officer Name
    FREEMER, MICHELLE M.
  • Budget Start Date
    12/15/2015 - 9 years ago
  • Budget End Date
    12/16/2015 - 9 years ago
  • Fiscal Year
    2016
  • Support Year
    01
  • Suffix
    A1
  • Award Notice Date
    12/14/2015 - 9 years ago
Organizations

Asthma symptom perception feedback intervention for ethnic minority adolescents

? DESCRIPTION (provided by applicant): Under-perception of asthma symptoms in children is a major risk factor for emergency department visits, hospitalizations, and near-fatal/fatal asthma attacks. Puerto Rican and Black children have greater asthma morbidity and mortality rates than all other racial/ethnic groups. Interventions targeting asthma symptom perception and medication adherence may help close this asthma health disparities gap. There are no RCT studies to date designed to improve asthma symptom perception in ethnic minority children. This R01 study builds upon this new investigator PI's prior grants. We demonstrated that children who did not receive peak expiratory flow (PEF) feedback under-perceived asthma symptoms 42% of the time vs. 15% for the PEF feedback group and had lower controller medication adherence (27.5% vs. 48.8%). The proposed randomized controlled trial consists of two arms: PEF feedback (N = 130) versus control feedback (N = 130). Latino and Black adolescents with asthma ages 10-17 years old and their caregivers will be recruited from clinics in the Bronx, NY. The primary aims are to examine the efficacy of PEF prediction with feedback versus control feedback on 1) under-perception of asthma symptoms 2) controller medication adherence and 3) asthma control and emergency health care use. These aims will be examined across a 1- year follow-up. An exploratory aim examines the hypothesized pathway that the PEF intervention reduces under-perception of symptoms, shifts illness representations toward the professional model and increases adolescents' and parents' asthma management self-efficacy, resulting in greater medication adherence and improved asthma control. The baseline visit for all families consists of standardized asthma education followed by 3 weeks of PEF prediction without feedback using a programmable, electronic spirometer. Participants then will be randomized to intervention group and their spirometer reprogrammed, showing either the actual PEF and daily asthma management messages (PEF feedback group) or a brief, positive message (control feedback group). For the next 6 weeks, all adolescents will predict their PEF, which will be locked in before blowing into the device. Families will return at mid-intervention and post-intervention to receive verbal individualized feedback on symptom perception and problem-solving skills training (PEF feedback group) or supportive counseling (control feedback group). All adolescents will play Quest for the Code to reinforce the baseline asthma education. At the post-intervention visit, the spirometer will be reprogrammed for all adolescents to provide no feedback for the next 4 weeks. These symptom perception data will be downloaded at 1-month post-intervention. Controller medication adherence will be monitored by electronic devices. Post-intervention sessions will take place at 3, 6, 9, and 12 months to collect adherence data and conduct spirometry. Physicians will be blinded to group assignment and rate asthma control using national guidelines. A 12-month retrospective medical record abstraction will compare emergency health care use for asthma between groups.

IC Name
NATIONAL HEART, LUNG, AND BLOOD INSTITUTE
  • Activity
    R01
  • Administering IC
    HL
  • Application Type
    1
  • Direct Cost Amount
    1
  • Indirect Cost Amount
  • Total Cost
    1
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    837
  • Ed Inst. Type
    GRADUATE SCHOOLS
  • Funding ICs
    NHLBI:1\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    BMIO
  • Study Section Name
    Behavioral Medicine, Interventions and Outcomes Study Section
  • Organization Name
    YESHIVA UNIVERSITY
  • Organization Department
    PSYCHOLOGY
  • Organization DUNS
    071036636
  • Organization City
    NEW YORK
  • Organization State
    NY
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    100333201
  • Organization District
    UNITED STATES