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Asthma In-Home Monitoring (AIM) Trial

NCT00282516 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2025-02-10

No results posted yet for this study

Summary

OBJECTIVE: Determine whether home asthma telemonitoring using store-and-forward technology improves outcomes when compared to in-person, office-based visits.

Conditions

  • Mild, Moderate and Severe Persistent Asthma as Defined by NHLBI-2 Guidelines

Interventions

PROCEDURE

In-home telemonitoring of pediatric patients with persistent asthma

Sponsors & Collaborators

  • U.S. Army Medical Research Acquisition Activity

    collaborator FED

  • Tripler Army Medical Center

    lead FED

Principal Investigators

  • Charles W Callahan, DO · Chief, Department of Pediatrics, Tripler Army Medical Center

  • Debora S Chan, PharmD · Department of Pediatrics, Tripler Army Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
6 Years
Max Age
17 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2003-04-30
Primary Completion
2004-04-30
Completion
2004-04-30

Countries

  • United States

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00282516 on ClinicalTrials.gov