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

C

Children's Hospital of Eastern Ontario

Status

Active, not recruiting

Conditions

Diabetes Mellitus, Type 1

Treatments

Other: MyChart Questionnaire

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Enrollment

200 estimated patients

Sex

All

Ages

Under 131 months old

Volunteers

No Healthy Volunteers

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)

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

200 participants in 2 patient groups

MyChart Questionnaire (Intervention Group)
Experimental group
Description:
Participants within the intervention group will complete the patient-facing EHR-enabled MyChart® questionnaire.
Treatment:
Other: MyChart Questionnaire
Standard Clinical Care (Control Group)
No Intervention group
Description:
Participants within the control group will undergo standard clinical care with no study intervention.

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Elias Abou-Assaly, BA; Saunya Dover, MSc

Data sourced from clinicaltrials.gov

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