Trials / Completed
CompletedNCT01167855
Reducing Asthma Disparities Through School-Based Telemedicine for Rural Children
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 823 (actual)
- Sponsor
- Arkansas Children's Hospital Research Institute · Academic / Other
- Sex
- All
- Age
- 7 Years – 14 Years
- Healthy volunteers
- Accepted
Summary
The overall goal of this proposal is to examine the efficacy of a school-based asthma telemedicine intervention in a predominately minority, low-income rural pediatric population.
Detailed description
A total of 1110 subjects will be enrolled in this research study. Five hundred forty (540) subjects will be between the ages of 7-14 years. The remaining 540 subjects will be comprised of the primary caregiver of the participants. Thirty (30) school nurse/s providing care to the 270 intervention participants will also be enrolled in the study. To test our hypotheses, the investigators will conduct a cluster randomized trial with 540 children, ages 7-14 years and their parent/guardian(s), to address the following specific aims: Specific Aim 1: Examine the efficacy of a school-based asthma telemedicine intervention in improving asthma-related health outcomes in an intervention group compared to children receiving usual care. Specific Aim 2: Determine the effects of a school-based asthma telemedicine intervention on asthma self-management skills of intervention caregivers and participants compared to a usual care group. The investigators will compare changes in asthma self-efficacy, quality of life, and knowledge between groups. Specific Aim 3: Determine the cost of the intervention in relation to health outcomes.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Asthma Education Sessions | Comprehensive asthma education sessions delivered via telemedicine. |
| OTHER | Asthma Health Assessment via Telemonitoring | Each intervention participant will undergo assessment of asthma via school-based telemonitoring to measure lung function and provide a self-report of asthma symptoms. |
| OTHER | Provider Treatment Prompt | A treatment prompt will be mailed to the primary care provider at baseline and 3 months. |
| OTHER | School Absenteeism | Absenteeism before and after the intervention will be compared in the intervention group and also will be compared to absentee rates of the usual care group. |
| OTHER | Prescription Filling Profile | Study personnel will monitor participants' prescription profiles. |
Timeline
- Start date
- 2011-05-25
- Primary completion
- 2017-02-01
- Completion
- 2017-02-01
- First posted
- 2010-07-22
- Last updated
- 2017-05-16
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01167855. Inclusion in this directory is not an endorsement.