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Using an Online Patient Monitoring System to Improve Care for Children With Chronic Conditions

Integrated Clinical Information Sharing System: Implementation and Mixed-Methods Evaluation of a Web-based Monitoring and Management System for Patients With Chronic Conditions

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02097355
Acronym
TriVoxHealth
Enrollment
946
Registered
2014-03-27
Start date
2014-12-31
Completion date
2019-12-31
Last updated
2020-07-14

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

Conditions

Asthma, Attention Deficit Hyperactivity Disorder, Autism Spectrum Disorder, Depression, Epilepsy

Keywords

chronic disease, patient portal, health information technology, patient provider communication, quality improvement

Brief summary

TriVox Health is an online system designed to make it easy for healthcare providers to monitor patients' disease symptoms and functioning over time and in between in-person visits (http://www.youtube.com/watch?v=VR1vcbx0Ef4). Using combined quality improvement and randomized clinical trial methods, we will evaluate the impact of TriVox on the health outcomes, patient/family experience of care, and healthcare utilization for children and adolescents with Attention Deficit Hyperactivity Disorder (ADHD), asthma, autism, depression, and epilepsy.

Detailed description

TriVox Health is a web-based patient management and monitoring system designed to track patients' disease symptoms and response to therapy over time. TriVox Health enables clinics to use electronic surveys to gather data remotely from multiple responders, including patients, parents/guardians, school personnel and ancillary providers, and view the responses in a timely manner via graphical, tabular, and narrative summary formats. This quality improvement (QI) initiative will implement TriVox as the standard of care for all patients who receive care for ADHD, asthma, autism, depression, and epilepsy within seven ambulatory specialties at Boston Children's Hospital. Patients and families will use TriVox to report on patient health status and will complete clinically-reTriVoxlevant questionnaires at routine intervals. Providers will use the information collected through TriVox to inform their clinical care of the patient/family. To evaluate the effectiveness of TriVox, we will conduct a 24-month phased, cluster randomized controlled trial (RCT) where we randomize providers to active vs. delayed-start to TriVox use, with patients clustered by provider (within specialties) for analytic purposes. Delayed-start providers will crossover to active TriVox use after 12 months. Patients/families will complete additional surveys in order to assess the system's actual or potential effects on patient/family-provider interactions, healthcare utilization and costs.

Interventions

OTHERTriVox for clinical care

Use TriVox disease modules to manage patients

Sponsors

Boston Children's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Pediatric patients with clinical diagnosis of ADHD, asthma, autism, depression, and/or epilepsy * Patient receives care for these diagnoses from providers in participating ambulatory clinics (Primary Care, Adolescent Medicine, Developmental Medicine, Neurology, Psychiatry) * Patient's primary caregiver enrolled in TriVox

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Change in caregiver-rated disease-specific symptomsBaseline to 12 monthsCaregiver-reported ratings on disease-specific symptom rating scale. For example, Vanderbilt ADHD Parent Rating Scale for ADHD; Asthma Control Test for asthma

Secondary

MeasureTime frameDescription
Number of patients with red flag alerts1 monthNumber of patients whose responses to clinical questionnaires trigger a red flag alert in ICISS
Change in caregiver-rated global functioningBaseline to 12 monthsCaregiver ratings on modified Clinical Global Assessment Scale
Experience of careBaseline and after every ambulatory visit for up to 84 monthsParticipant ratings on Post-Visit Experience of Care Survey

Other

MeasureTime frameDescription
Healthcare utilization12 monthsinpatient and ambulatory visits within healthcare system directly related to patient's medical or mental health condition
Direct out of pocket expenditures12 monthsOut of pocket expenditures directly related to care for child's medical or mental health condition, e.g. co-pays, prescription costs

Countries

United States

Outcome results

None listed

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