Asthma Clinical Trial
— PAALOfficial title:
Pediatric Asthma Alert Intervention for Minority Children
| Verified date | June 2011 |
| Source | Johns Hopkins University |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | United States: Institutional Review Board |
| Study type | Interventional |
Young inner-city children with asthma have the highest emergency department (ED) visit
rates. Relying on the emergency department for asthma care can be a dangerous sign of poorly
controlled asthma. This research will focus on whether having a specialized asthma nurse
join the family at a child's doctor visit after an ED visit for asthma to make sure the
child and parent keep the follow-up appointment and have the nurse remind the child's doctor
to prescribe preventive asthma medicines and an asthma action plan for home (PAAL
intervention) will result in young children with asthma having fewer days with wheezing and
cough.
The investigators hypothesize that:
1. Significantly more children receiving the PAAL intervention will attend greater than 2
non-urgent visits and greater than 6 refills for the child's anti-inflammatory
medications over 12 months when compared to children in the control or standard asthma
education group.
2. Children in the PAAL intervention group will experience less morbidity and caregivers
will experience increased quality of life compared to children in the control of
standard asthma education group.
| Status | Completed |
| Enrollment | 350 |
| Est. completion date | June 2013 |
| Est. primary completion date | June 2013 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 3 Years to 10 Years |
| Eligibility |
Inclusion Criteria: All 6 criteria must be met: 1. Physician-diagnosed asthma (based on caregiver report with validation from the child's physician) 2. > 2 ED visits or > 1 hospitalization for asthma within past 12 months 3. Mild persistent to severe persistent asthma based on NHLBI guidelines criteria (7-9) having any 1 of the following: - An average of > 2 days per week of asthma symptoms - > 2 days per week with rescue medication use (albuterol, xopenex) OR - > 2 days per month of nighttime symptoms 4. Age > 3 and < 10 years 5. Reside in Baltimore Metropolitan area 6. Not currently participating in another asthma study or sibling enrolled in PAAL study Exclusion Criteria: 1. Inability to speak and understand English 2. No access to a working phone or alternate phone for follow-up surveys 3. Co-morbid respiratory condition including cystic fibrosis, chronic lung disease (BPD), lung cancer, tracheostomy that could interfere with the assessment of asthma-related outcome measures. 4. Children residing in foster care or where consent cannot be obtained from a legal guardian. |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Prevention
| Country | Name | City | State |
|---|---|---|---|
| United States | Johns Hopkins University | Baltimore | Maryland |
| Lead Sponsor | Collaborator |
|---|---|
| Johns Hopkins University | University of Maryland, University of Rochester |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Number of primary care appointments kept over 12 months | 12 months | No | |
| Secondary | Number of refills for anti-inflammatory medications prescribed over 12 months | 12 months | No |
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