Informing Policy to Implement Pediatric Family Engagement in Meaningful Use Stage 3
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ClinicalTrials.gov Identifier: NCT01966068 |
Recruitment Status :
Completed
First Posted : October 21, 2013
Results First Posted : August 30, 2016
Last Update Posted : October 17, 2016
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This study will enroll parents/guardians of children who receive treatment at one of the pediatric primary care practice settings in the Pediatric Research in Office Settings (PROS) network or at the Children's Hospital of Philadelphia's Pediatric Research Consortium (PeRC) network.
The study will use an evidence-based conceptual model to study determinants of implementation success, implementation outcomes, and health care outcomes resulting from implementing an already functional, electronic health record (EHR)-linked asthma portal, MyAsthma. The study will measure the portal's feasibility and determine the impact on providing asthma education and fostering patient engagement as well as the ability to collect patient-reported outcomes for children, evaluate medication use and side effects and track parents' preferences and goals.
Condition or disease | Intervention/treatment | Phase |
---|---|---|
Asthma | Other: MyAsthma Web Portal | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 294 participants |
Allocation: | N/A |
Intervention Model: | Single Group Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Health Services Research |
Official Title: | Informing Policy to Implement Pediatric Family Engagement in Meaningful Use Stage 3 |
Study Start Date : | October 2013 |
Actual Primary Completion Date : | February 2015 |
Actual Study Completion Date : | February 2015 |

Arm | Intervention/treatment |
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Experimental: MyAsthma Web Portal
The portal, MyAsthma, will provide asthma education, collect patient-reported outcomes, evaluate medication use and side effects, and track parents' concerns and goals. Parents will log into the web portal each month (for a total of 3 portal visits in 6 months), and the information entered by parents will be shared through the electronic health record with the child's primary care provider.
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Other: MyAsthma Web Portal
Parents will log on to the MyAsthma Web Portal up to three different times over a 6 month period. During each portal visit, parents will be asked to complete a survey which will include questions regarding their views on treatment preferences, goals, asthma control, and medications for their child with asthma. |
- Difference Between Number of Families Who Adopted MyAsthma Portal Use and Number of Families With Sustained Use [ Time Frame: Up to 6 Months ]Implementation success was measure by comparing the of the number of enrolled families (parent/guardian) who logged on to the MyAsthma Portal once (adoption) with the number of enrolled families (parent/guardian) who logged on more than once (sustained use). Parents/guardians were asked to log on and complete the same survey on the MyAsthma Portal 3 times during a 6 month period.

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Ages Eligible for Study: | Child, Adult, Older Adult |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria For Parents/Guardians:
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Parent/guardian of a child who:
- Is between the ages of 6-12 years old
- Has a diagnosis of asthma on his/her problem list at the time of recruitment
- Has had an office visit with asthma as a diagnosis within the past 12 months
- Must be able to speak and read English
Exclusion Criteria For Parents/Guardians:
- Child has not had an office visit for asthma with in the last 12 months
- Parent or guardian does not speak or read English

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01966068
United States, Illinois | |
Pediatrick Research in Office Settings (PROS) | |
Elk Grove Village, Illinois, United States, 60007 | |
United States, Pennsylvania | |
Pediatric Research Consortium of the Children's Hospital of Philadelphia (PeRC) | |
Philadelphia, Pennsylvania, United States, 19104 |
Principal Investigator: | Alexander Fiks, MD, MSCE | Children's Hospital of Philadelphia |
Responsible Party: | Children's Hospital of Philadelphia |
ClinicalTrials.gov Identifier: | NCT01966068 |
Other Study ID Numbers: |
13-010285 |
First Posted: | October 21, 2013 Key Record Dates |
Results First Posted: | August 30, 2016 |
Last Update Posted: | October 17, 2016 |
Last Verified: | August 2016 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | Undecided |
Asthma Pediatrics Health Technology Meaningful Use Stage-3 Web Portal |
Asthma Bronchial Diseases Respiratory Tract Diseases Lung Diseases, Obstructive Lung Diseases |
Respiratory Hypersensitivity Hypersensitivity, Immediate Hypersensitivity Immune System Diseases |