Clinical trial · Interventional
Asthma In-Home Monitoring (AIM) Trial
"Internet-based Home Monitoring and Education of Children With Asthma is Comparable to Ideal, Office-based Care: Results of a One-year, Asthma In-Home Monitoring (AIM) Trial"
NCT00282516CI-TRIAL-00085695completedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
OBJECTIVE: Determine whether home asthma telemonitoring using store-and-forward technology improves outcomes when compared to in-person, office-based visits.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Mild, Moderate and Severe Persistent Asthma as Defined by NHLBI-2 Guidelines | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| In-home telemonitoring of pediatric patients with persistent asthma | Procedure | — | UNRESOLVED |
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 6 Years
- Maximum age
- 17 Years
Show eligibility criteria text
Inclusion Criteria: * Diagnosis of persistent asthma as defined using the NHLBI Expert Panel Report -2 guidelines Assignment of severity classification will be made at the beginning of the study based on severity of disease off therapy. * Dependent of active duty or retired US military personnel * 6 to 17 years of age * Not moving from Oahu for 12 months after entry into study * Ability to receive cable modem hook-up in home * Willingness to learn to record and send MDI + spacer technique and peak flow two times week * Willing to attend asthma education follow-up visits either in person or electronically at 2- weeks, 6- weeks, 3-months and 6-month intervals after initiation into the study. * Willing to complete survey at the end of study period. * Willing to sign informed, written consent Exclusion Criteria: * Diagnosis of mild intermittent asthma as defined by Expert Panel Report -2 guidelines. * \<6 and \>17 years of age * Family leaving Oahu within 12 months * Inability to receive cable modem hook-up in home * Unwilling or unable to learn to record and send MDI + spacer technique and peak flow and/or to attend asthma education follow-up visits either in person or electronically at initiation into study and at 2- weeks, 6- weeks, 3-months and 6 month intervals. * Unwilling to complete survey at the end of study period. * Patients or parents who decline to participate. * Patients with other chronic pulmonary disease (cystic fibrosis, bronchopulmonary dysplasia)
References
Publications (0)
Data not yet available
No reference posted for this study.