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Evaluation of a Shared Decision Making Portal for Pediatric Asthma

Evaluation of a Shared Decision Making Portal for Pediatric Asthma

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01715389
Enrollment
81
Registered
2012-10-29
Start date
2012-11-30
Completion date
2015-03-31
Last updated
2015-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asthma

Keywords

Asthma, Goals, Shared Decision Making, Patient Portal, Electronic Medical Record

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.

Interventions

OTHERMyAsthma Patient Portal

Parents in the intervention group will use the MyAsthma Patient Portal to receive enhanced educational information on asthma and its treatment, identify concerns and goals related to asthma treatment, track progress toward goals and management of concerns monthly, and track asthma symptoms monthly. Clinicians seeing intervention families at office visits will have access to information from the portal including concerns, goals, progress toward goals, and tracking of asthma symptoms.

Sponsors

Children's Hospital of Philadelphia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
6 Years to 12 Years
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

Design outcomes

Primary

MeasureTime frameDescription
Acceptability of the intervention to parents and clinicians24 monthsParents 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

MeasureTime frameDescription
Parent Activation0 months, 3 months, 6 monthsParent activation will be measured by the Parent Patient Activation Measure (PPAM).
Goal Attainment0 months, 3 months, 6 months then MonthlyParents will identify one or more goals at the study start. Progress toward the goal(s) will be assessed at 3 and 6 month follow-up using Likert-scaled items for the control group, and monthly through use of the portal for the intervention group.
Asthma-Related Quality of Life0 months, 6 monthsAsthma-related quality of life will be measured using The Integrated Therapeutics Group Child Asthma Short Form (ITG-CASF)
Asthma Control0 months, 6 monthsAsthma control will be assessed using the Pediatric Asthma Control Tool (PACT)
Shared decision makingBaselineJoint participation in decision-making will be measured by the Observing Parent Involvement (OPTION) scale.
Asthma Medication Adherence/Receipt6 monthsPrescribed medications for the treatment and management of asthma Type and number of prescriptions for asthma
Feasibility of Recruitment24 monthsThe feasibility of recruitment will be assessed by examining the proportion of all families contacted who meet enrollment criteria and the proportion of families meeting enrollment criteria who enroll.
Feasibility of Follow-up24 monthsThe feasibility of follow-up will be assessed by the proportion of enrolled families who complete each study measure.
Feasibility of Portal Use24 monthsThe feasibility of portal use will be assessed by the level of research team/other outside support needed.
Asthma-related Utilization3 months, 6 monthsUtilization will be measured by parent report and chart review by the research team of the following: Any primary care or subspecialty outpatient encounters relevant to asthma care, asthma-specific acute primary care visits or Urgent Care Center visits, asthma-specific Emergency Room visits, asthma-specific hospital admissions.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026