A randomized clinical trial to reduce asthma morbidity among inner-city children: Results of the National Cooperative Inner-City Asthma Study

Objective: To evaluate a family-focused asthma intervention designed for in ner-city children 5 to 11 years old with moderate to severe asthma. Study design: Randomized, multisite, controlled trial to minimize symptom d ays (wheeze, loss of sleep, reduction in play activity) measured by a 2-wee k recall assessed at 2-month intervals over a 2-year follow-up period. The intervention was tailored to each family's individual asthma risk. profile assessed at baseline. Results: Averaged over the first 12 months, participants in the interventio n group (n = 515) reported 3.51 symptom days in the 2 weeks before each fol low-up interview compared with 4.06 symptom days far the control group (n = 518), a difference of 0.55 (95% CI, 0.18 to 0.92, P = .004). The reduction among children with severe asthma was approximately 3 times greater (1.54 d/2 wk). More children in the control group (18.9%) were hospitalized durin g the intervention compared with. children in the intervention group (14.8% ), a decrease of 4.19% (CI, -8.75 to 0.36, P = .071). These improvements we re maintained in the intervention group during the second year of follow-up , during which they did not have access to the asthma counselor Conclusions: We demonstrated that an individually tailored, multifaceted in tervention carried out. by Masters-level social workers trained in asthma m anagement can reduce asthma symptoms among children in the inner city.