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Clinical Trials/NCT01715389
NCT01715389CompletedNot Applicable

Evaluation of a Shared Decision Making Portal for Pediatric Asthma

Children's Hospital of Philadelphia2 sites in 1 country81 target enrollmentStarted: November 2012Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
81
Locations
2
Primary Endpoint
Acceptability of the intervention to parents and clinicians

Study Overview

Brief Summary

This pilot intervention study will test the feasibility and acceptability and explore the outcomes of a primary care-based shared decision making (SDM) electronic medical record (EMR)-based portal that provides education, elicits and tracks patients/families' treatment concerns and goals, assesses symptoms and asthma control over time, and provides decision support to clinicians and families.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
6 Years to 12 Years (Child)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Parents/legal guardians of children aged 6-12 with persistent asthma, currently receiving chronic maintenance therapy, cared for at a study practice, with consistent access to a computer with an internet connection where they feel comfortable accessing MyChart (patient portal)
  • Clinician at study site

Exclusion Criteria

  • parents non-english speaking
  • child's primary care provider at the time of enrollment is a pediatric resident
  • not meeting inclusion criteria

Outcomes

Primary Outcomes

Acceptability of the intervention to parents and clinicians

Time Frame: 24 months

Parents and clinicians will be asked a series of open-ended questions regarding themes including satisfaction, acceptability and unintended consequences of using the portal for intervention subjects and using MyChart in general for control subjects. Subjects will also be asked a series of Likert-scaled questions related to satisfaction.

Secondary Outcomes

  • Feasibility of Portal Use(24 months)
  • Shared decision making(Baseline)
  • Goal Attainment(0 months, 3 months, 6 months then Monthly)
  • Parent Activation(0 months, 3 months, 6 months)
  • Asthma-Related Quality of Life(0 months, 6 months)
  • Asthma Control(0 months, 6 months)
  • Asthma-related Utilization(3 months, 6 months)
  • Asthma Medication Adherence/Receipt(6 months)
  • Feasibility of Recruitment(24 months)
  • Feasibility of Follow-up(24 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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