Web-Based and Tailored Asthma Management Intervention (Puff City) in Teens With Asthma Attending Urban Clinics (PCC)
Primary Purpose
Asthma
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Teens randomized to the experimental arm will receive 4 sessions plus a booster of web-based, tailored asthma management.
Teens in the control group will receive generic, web-based asthma education.
Sponsored by

About this trial
This is an interventional other trial for Asthma focused on measuring Urban adolescents, Acute asthma, Asthma, Computer tailoring, Web-based intervention, Puff City
Eligibility Criteria
Inclusion Criteria:
- 13-19 years of age
- Must be able to provide electronic assent and have consent from a parent/guardian if applicable
Diagnosis of asthma by meeting one of the following criteria within the last 12 months:
- At least one emergency department diagnosis of asthma or
- At least one acute inpatient encounter with asthma as the principal diagnosis or
- At least four outpatient visits with an asthma diagnosis and at least 2 asthma medications dispensed or
- At least four asthma medications dispensed
Exclusion Criteria:
- Inability to provide informed consent/assent
- Lack of physician diagnosis of asthma
- Other co-morbidities that make it impossible for the individual to participate.
Sites / Locations
- Henry Ford Health System
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Tailored asthma management program
Control
Arm Description
Teens randomized to the experimental arm will receive 4 sessions plus a booster of web-based, tailored asthma management.
Teens in the control group will receive generic, web-based asthma education.
Outcomes
Primary Outcome Measures
Asthma Control Test (ACT)
Comparison of ACT scores at 12 months after the randomization
Secondary Outcome Measures
Asthma Exacerbations/Functional Status
Comparison of asthma exacerbations (asthma hospitalizations, emergency department visits, or oral corticosteroid dispensing)and functional status(e.g. self report of symptom-days, symptom nights, days of restricted activity, school/work days missed) at 12 months after randomization.
Full Information
NCT ID
NCT01757002
First Posted
December 7, 2012
Last Updated
August 8, 2017
Sponsor
Henry Ford Health System
Collaborators
University of Michigan, Augusta University, National Heart, Lung, and Blood Institute (NHLBI)
1. Study Identification
Unique Protocol Identification Number
NCT01757002
Brief Title
Web-Based and Tailored Asthma Management Intervention (Puff City) in Teens With Asthma Attending Urban Clinics
Acronym
PCC
Official Title
Pragmatic Randomized Controlled Trial of the Web-Based Asthma Management Intervention (Puff City) in Teens With Asthma Attending Urban Clinics
Study Type
Interventional
2. Study Status
Record Verification Date
August 2017
Overall Recruitment Status
Completed
Study Start Date
March 2013 (undefined)
Primary Completion Date
May 2015 (Actual)
Study Completion Date
November 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Henry Ford Health System
Collaborators
University of Michigan, Augusta University, National Heart, Lung, and Blood Institute (NHLBI)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to evaluate the Puff City web-based behavioral intervention of asthma management program in a clinical setting. This study also examines and evaluates the cost and efficiency of patient eligibility determination methods, patient recruitment, study monitoring (compliance with study regimen, participant retention and follow-up), and the collection of clinical endpoints.
Detailed Description
Asthma continues to be a major public health problem in the US with high economic and social costs. Vulnerable ethnic communities are disproportionately affected by asthma as demonstrated by higher morbidity and mortality for these groups. We have completed two school-based, randomized trials of a web-based, computer-tailored asthma management intervention that targets urban teens (Puff City).
The current study, Puff City in the Clinic, will be evaluated as a clinical tool by initiating the web-based behavioral intervention of asthma management in a clinical setting. However, the current paradigm for conducting such a trial is costly with respect to patient recruitment, intervention delivery, and data collection and management. To address these high costs, the study utilizes comparative effectiveness research (CER) pragmatic approaches to design a randomized controlled trial for patient recruitment and determination of eligibility, study monitoring (compliance with study regimen, participant retention and follow-up), and collection of clinical endpoints.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma
Keywords
Urban adolescents, Acute asthma, Asthma, Computer tailoring, Web-based intervention, Puff City
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
266 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Tailored asthma management program
Arm Type
Experimental
Arm Description
Teens randomized to the experimental arm will receive 4 sessions plus a booster of web-based, tailored asthma management.
Arm Title
Control
Arm Type
Active Comparator
Arm Description
Teens in the control group will receive generic, web-based asthma education.
Intervention Type
Behavioral
Intervention Name(s)
Teens randomized to the experimental arm will receive 4 sessions plus a booster of web-based, tailored asthma management.
Intervention Description
Web-based, computer-tailored asthma management intervention delivered in 4 sessions, plus a 6 month booster.
Intervention Type
Behavioral
Intervention Name(s)
Teens in the control group will receive generic, web-based asthma education.
Intervention Description
Web-based, generic asthma management intervention delivered in 4 sessions.
Primary Outcome Measure Information:
Title
Asthma Control Test (ACT)
Description
Comparison of ACT scores at 12 months after the randomization
Time Frame
12 Months
Secondary Outcome Measure Information:
Title
Asthma Exacerbations/Functional Status
Description
Comparison of asthma exacerbations (asthma hospitalizations, emergency department visits, or oral corticosteroid dispensing)and functional status(e.g. self report of symptom-days, symptom nights, days of restricted activity, school/work days missed) at 12 months after randomization.
Time Frame
12 Months
Other Pre-specified Outcome Measures:
Title
The Cost
Description
The cost of study intervention will be evaluated: The cost for participant enrollment with Electronic Medical Record (EMR) initiation; data collection and management with/o EMR initiation including assessing the reliability of EMR clinical outcomes/primary endpoints, compared to chart abstraction.
Time Frame
Up to 12 months
Title
The Cost Effectiveness
Description
The cost effectiveness of Puff City intervention compared to controls without study intervention.
Time Frame
Up to 12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
13 Years
Maximum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
13-19 years of age
Must be able to provide electronic assent and have consent from a parent/guardian if applicable
Diagnosis of asthma by meeting one of the following criteria within the last 12 months:
At least one emergency department diagnosis of asthma or
At least one acute inpatient encounter with asthma as the principal diagnosis or
At least four outpatient visits with an asthma diagnosis and at least 2 asthma medications dispensed or
At least four asthma medications dispensed
Exclusion Criteria:
Inability to provide informed consent/assent
Lack of physician diagnosis of asthma
Other co-morbidities that make it impossible for the individual to participate.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mei Lu, PhD
Organizational Affiliation
Henry Ford Health System
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Christine Joseph, PhD
Organizational Affiliation
Henry Ford Health System
Official's Role
Principal Investigator
Facility Information:
Facility Name
Henry Ford Health System
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48202
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
24607295
Citation
Lu M, Ownby DR, Zoratti E, Roblin D, Johnson D, Johnson CC, Joseph CL. Improving efficiency and reducing costs: Design of an adaptive, seamless, and enriched pragmatic efficacy trial of an online asthma management program. Contemp Clin Trials. 2014 May;38(1):19-27. doi: 10.1016/j.cct.2014.02.008. Epub 2014 Mar 6.
Results Reference
derived
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Web-Based and Tailored Asthma Management Intervention (Puff City) in Teens With Asthma Attending Urban Clinics
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