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Clinical Trials in Canada / NCT05979077
Active, not recruiting Not applicable

Children's Hospital Academic Medical Organization (CHAMO) MyChart Study

NCT05979077 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2023-04-03
Last updated
2025-04-15

Condition(s) studied

Diabetes Mellitus, Type 1

Investigational drug(s) / intervention(s)

MyChart Questionnaire

MyChart Questionnaire: Prior to clinic visits, families completing the MyChart Questionnaire will enter details about their current management and visit goals, automatically populating their electronic health record for subsequent review/revision by the health care team before and during the visit, reallocating clinic time previously used for data acquisition to individual patient priorities

Study summary

Evolving technology and clinical innovation have led to dramatic changes in the management of type 1 diabetes (T1D). These changes have led to a need to collect a growing number of details from families during their visits. As a result, much of the physician-patient visit is spent transferring information instead of focusing on diabetes care, contributing to increased time pressures in clinic and unmet needs for patients.

In response to this reality, the investigators have developed a tool that allows families to input their diabetes-related information into their physicians' electronic health record (EHR) documentation tool before their clinic visit, using a questionnaire administered via CHEO's secure patient portal (MyChart®). The investigators will evaluate the impact of an integrated electronic patient questionnaire, on quality of care (patient-reported), diabetes control and clinic efficiency. The investigators hope that our study will determine whether having families input clinical data prior to a visit is an effective strategy to improve the quality of diabetes care. The investigators believe that the findings will be of interest to all those studying the value of incorporating patient-entered data both within diabetes care and beyond.

Eligibility

Sex
ALL
Min age
0 Years
Max age
131 Months
Healthy volunteers
No
Inclusion Criteria: * Diagnosis of T1D * Age \<11 years at enrollment Exclusion Criteria: * Patients ≥ 11 years of age at enrollment * Patients who are not fluent enough in English to complete all study related procedures * Patients unable or unwilling to provide consent and/or assent * Patients followed in Eating Disorder Clinic or Child and Youth Protection Clinic (there are MyChart activation restrictions for individuals followed in these clinics)

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Children's Hospital of Eastern Ontario - Research Institute Ottawa Ontario

More Children's Hospital of Eastern Ontario trials in Canada

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05979077 on ClinicalTrials.gov ↗ ← All trials in Canada