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Clinical Trials/NCT00521105
NCT00521105
Completed
Not Applicable

Assessment of an Alternative Model Using Telemedicine Follow-up of Children and Adolescents With Type 1 Diabetes

University of Calgary1 site in 1 country82 target enrollmentAugust 2005

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Type 1 Diabetes Mellitus
Sponsor
University of Calgary
Enrollment
82
Locations
1
Primary Endpoint
Medical outcomes: HbA1c, rates of severe hypoglycemia, rates of DKA
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

The purpose of the study is to look at the effect of replacing the physician only visit by a transmission of information on the participant's current diabetes management and blood glucose monitoring results followed by a phone contact by the diabetes nurse educator. The study will also measure the effect on diabetes control (HbA1c), satisfaction with care, resource utilisation, and costs to the health care system and to the participant.

We hypothesize that replacement of the physician-only visit by a virtual visit will not result in worsening of the medical outcomes and that it will result in a reduction in medical resources utilization and costs for families while increasing the satisfaction with care.

Detailed Description

Improved metabolic control reduces both the onset and progression of diabetes-related complications in adults and adolescents with type 1 diabetes. Frequency of contact with the medical care team has been associated with better control. Both the American Diabetes Association and Canadian Diabetes Association recommend regular quarterly visits. However, the increase in case loads and the limited manpower available forces us to look at alternative models of care. A model of care in which medical visits alternate between a face to face multidisciplinary visits and a virtual visit done via fax or e-mail communication and a phone call may be advantageous to both the patient and the medical care team. For the patient and his family, this model would decrease time away from school and work, travel inconveniences and costs. For the medical care team it may decrease time per patient and therefore increase the number of patients served with the same resources.

Registry
clinicaltrials.gov
Start Date
August 2005
End Date
November 2009
Last Updated
14 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dr. Danièle Pacaud

Pediatric Endocrinologist

University of Calgary

Eligibility Criteria

Inclusion Criteria

  • Children: 17 years of age or less
  • Diagnosis of Type 1 Diabetes for at least 12 months
  • Currently being followed at the Alberta Children's Hospital Diabetes Clinic.

Exclusion Criteria

  • Compromised metabolic control (HbA1c \> 10%)
  • Uncontrolled hypo or hyperthyroidism
  • Uncontrolled celiac disease
  • Language or psychosocial barrier preventing the family from completing the study
  • Diabetes duration of less than 1 year
  • Participation in other clinical trials with specified clinic visits.

Outcomes

Primary Outcomes

Medical outcomes: HbA1c, rates of severe hypoglycemia, rates of DKA

Time Frame: 1 year

Secondary Outcomes

  • Resource utilization: physicians, nurses, and dietitians, emergency room visits(1 year)
  • Family satisfaction with diabetes care(1 year)
  • Associated costs to the family (time away from school and work, travel, etc)(1 year)

Study Sites (1)

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