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Enhanced Asthma Monitoring Technology for Childhood Asthma (EMT Trial)

N/A
Waitlist Available
Research Sponsored by Nemours Children's Clinic
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24 weeks
Awards & highlights

EMT Trial Summary

This trial looks to see if a home monitoring program can help kids with asthma manage their symptoms.

Who is the study for?
This trial is for children with persistent asthma who have access to a mobile device with internet, are followed by certain primary care practices, and can perform lung function tests. It's not for non-English speakers or those with serious heart/lung conditions besides asthma.Check my eligibility
What is being tested?
The study is testing a home monitoring program for childhood asthma that includes remote visits and lung function testing via a mobile app. It aims to assess the feasibility, acceptability, accessibility of the program, and its impact on asthma control.See study design
What are the potential side effects?
Since this trial involves monitoring technology rather than medication, traditional side effects aren't expected. However, there may be indirect effects related to using the technology or potential stress from frequent health monitoring.

EMT Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and 24 weeks for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Acceptability
Accessibility
Feasibility (Completion of study measures including generation of mobile spirometry results)
+1 more
Secondary outcome measures
Explore asthma-related factors associated with successful completion of the intervention.
Explore patient and family-related demographic characteristics and psychosocial factors associated with successful completion of the intervention.
Explore the preliminary effectiveness of the pilot program on asthma control.
+1 more

EMT Trial Design

1Treatment groups
Experimental Treatment
Group I: Pilot study arm for technology-enhanced asthma interventionExperimental Treatment1 Intervention
All participants will be in the pilot arm for technology-enhanced intervention program.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Pilot study arm for technology-enhanced asthma intervention
2023
N/A
~20

Find a Location

Who is running the clinical trial?

Nemours Children's ClinicLead Sponsor
124 Previous Clinical Trials
18,116 Total Patients Enrolled
National Institute of General Medical Sciences (NIGMS)NIH
268 Previous Clinical Trials
248,745 Total Patients Enrolled

Media Library

Childhood Asthma Clinical Trial 2023: Pilot study arm for technology-enhanced asthma intervention Highlights & Side Effects. Trial Name: NCT05824936 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Is this trial allowing minors to participate?

"This clinical trial is specifically recruiting patients aged 12 to 18; accordingly, there are 141 trials available for individuals in this age range and 216 studies catering to those over 65."

Answered by AI

Am I eligible to participate in this research endeavor?

"Aspiring participants of this trial must have a childhood history with asthma and fall within the age range between 12-18 years old. The study is planning to accept 15 enrollees in total."

Answered by AI

Are there any slots available for potential participants in this research endeavor?

"Clinicaltrials.gov verifies that the subject trial, which initially became available on May 15th 2023, is not currently seeking participants. However, there are 347 other clinical trials open to enrolment at this time."

Answered by AI

What objectives are being sought in this experiment?

"The principal aim of this 24-week study is to determine the feasibility, which includes the generation of mobile spirometry results. Secondary objectives include characterizing asthma-related factors associated with successful completion of the intervention via a questionnaire, exploring the preliminary effectiveness on asthma control through an ACT score assessment, and measuring daytime sleepiness using ESS-CHAD scores in order to measure efficacy."

Answered by AI
~8 spots leftby Apr 2025