Reducing Asthma Disparities Through School-Based Telemedicine for Rural Children
Asthma, Quality of Life, Children

About this trial
This is an interventional health services research trial for Asthma focused on measuring Pediatric Asthma, Low-income, Arkansas Delta Region
Eligibility Criteria
Inclusion Criteria:
The investigators will recruit students (ages 7-14 years) with asthma who are currently enrolled in public school districts located in the Delta region of Arkansas.
Eligibility of identified children will be determined by a brief telephone survey. The survey questions will determine if the child fulfills inclusion/exclusion criteria.
- Age ≥ 7 and ≤ 14 years.
- Use of asthma medications for acute relief of symptoms (rescue) or for control of symptoms (preventive) in the past 6 months. Children not on a controller who report using a rescue medication only for prevention of exercised-induced symptoms will not be eligible for the study.
- Physician-diagnosed asthma by parent/caregiver report. OR
In the absence of a formal physician diagnosis, the caregiver must report symptoms consistent with at least mild persistent asthma. The investigators will use asthma screening criteria to ensure that participants meet eligibility requirements. Participants must establish a history of episodic airflow obstruction or airway hyperresponsiveness and meet National Heart Lung and Blood Institute (NHLBI) guidelines for persistent asthma. Mild persistent asthma will be defined as any 1 of the following during the prior 4 weeks (by caregiver report):
- An average of > 2 days per week with asthma symptoms
- > 2 days per week with rescue medication use
- > 2 nights per month awakened with nighttime symptoms
- Minor limitation of activity
- ≥ 2 episodes of asthma during the past year that have required systemic corticosteroids
Exclusion Criteria:
- Significant underlying respiratory disease other than asthma (such as cystic fibrosis or chronic lung disease) that could potentially interfere with asthma-related outcome measures.
- Significant co-morbid conditions (such as severe developmental delay) that could preclude participation in an education-based intervention.
- Inability to speak or understand English (child or parent).
- Children in foster care or other situations in which consent cannot be obtained from a guardian.
- Prior enrollment in the study.
- Families without access to a working telephone as all survey data will be collected via telephone.
Sites / Locations
- Arkansas Children's Hospital Research Institute
Arms of the Study
Arm 1
Experimental
Intervention
Telemedicine asthma education sessions Asthma health assessment via telemonitoring Provider treatment prompts School absenteeism Prescription filling profile