Childhood Asthma Perception Study
Status: | Recruiting |
---|---|
Conditions: | Asthma |
Therapuetic Areas: | Pulmonary / Respiratory Diseases |
Healthy: | No |
Age Range: | 10 - 17 |
Updated: | 3/8/2019 |
Start Date: | May 2016 |
End Date: | November 2020 |
Contact: | Jonathan Feldman, PhD |
Email: | jonathan.feldman@einstein.yu.edu |
Phone: | 646-592-4539 |
This randomized controlled trial will include Latino and Black adolescents with asthma ages
10-17 years old and their caregivers. Participants will be recruited from clinics in the
Bronx, NY. The primary aims are to examine the efficacy of peak expiratory flow (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.
10-17 years old and their caregivers. Participants will be recruited from clinics in the
Bronx, NY. The primary aims are to examine the efficacy of peak expiratory flow (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.
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.
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 or control feedback group and
receive a brief feedback session. 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 feedback sessions. All adolescents will
play an interactive asthma educational game to reinforce the baseline asthma education. At
the post-intervention visit, the spirometer will be reprogrammed 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 severity using national
guidelines. A 12-month retrospective medical record abstraction will compare emergency health
care use for asthma between groups.
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.
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 or control feedback group and
receive a brief feedback session. 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 feedback sessions. All adolescents will
play an interactive asthma educational game to reinforce the baseline asthma education. At
the post-intervention visit, the spirometer will be reprogrammed 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 severity using national
guidelines. A 12-month retrospective medical record abstraction will compare emergency health
care use for asthma between groups.
Inclusion Criteria:
- 10-17 years of age
- Diagnosis of asthma (in medical record)
- Report of breathing problems within the past 12 months
- Prescribed a controller medication for asthma
- At least one parent self-identifies as Latino or Black
- The participating parent has primary or at least equal responsibility for the
adolescent
Exclusion Criteria:
- Cognitive learning disability (parent report)
- No prescription for asthma controller medication
- Inability to perform acceptable PEF blows
- Race/ethnicity other than Latino or Black
- Other significant pulmonary conditions (cystic fibrosis)
We found this trial at
2
sites
3550 Jerome Avenue
Bronx, New York 10467
Bronx, New York 10467
(718) 920-4321
Phone: 718-405-8090
Montefiore Medical Center As the academic medical center and University Hospital for Albert Einstein College...
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1400 Pelham Parkway South
Bronx, New York 10461
Bronx, New York 10461
(718) 918-5000
Phone: 718-918-6984
Jacobi Medical Center In 1955, the NYC Department of Hospitals opened a new, specialized care...
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