Feasibility of an ED Initiated Online Asthma Management Program for Urban Teens

NCT01695031 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 126

Last updated 2015-04-01

No results posted yet for this study

Summary

The objective of this study is to determine the feasibility of conducting a randomized controlled trial to evaluate the effectiveness of an online, Emergency Department-initiated asthma management intervention designed to reduce asthma-related morbidity among urban teenagers aged 13-19 years with uncontrolled asthma. The study will examine issues around recruitment, participant compliance with the study protocol, Internet access, and attrition. Investigators will first develop a protocol for recruiting 13-19 year old patients with acute asthma into an ED-initiated pilot trial of an online asthma management program, describing recruitment and refusal rates. Investigators will measure participant compliance with the pilot study protocol including 4 online sessions and a 6 month survey. Investigators will also measure compliance of the participants parents at baseline and a six month follow up. Investigators will then use pilot study results to describe the intervention effect on selected outcomes including ED visits, asthma control as measured by Asthma Control Questionnaire, functional limitations, quality of life, and behavior change.

Conditions

  • Acute Asthma

Interventions

BEHAVIORAL

Tailored asthma management program

web-based, computer-tailored asthma management intervention delivered every week for 4 weeks

BEHAVIORAL

Generic web-based education

Generic, web-based asthma education

Sponsors & Collaborators

  • University of Michigan

    collaborator OTHER
  • Children's Hospital of Michigan

    collaborator OTHER
  • Augusta University

    collaborator OTHER
  • Henry Ford Health System

    lead OTHER

Principal Investigators

  • Christine LM Joseph, PhD, MPH · Henry Ford Health System

Study Design

Allocation
RANDOMIZED
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
13 Years
Max Age
19 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-10-31
Primary Completion
2015-03-31
Completion
2015-03-31

Countries

  • United States

Study Locations

More Related Trials

Entities

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 NCT01695031 on ClinicalTrials.gov