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Clinical Trials/NCT01058733
NCT01058733
Completed
Not Applicable

Seoul St. Mary's Hospital College of Medicine The Catholic University of Korea, Seoul, Korea

The Catholic University of Korea1 site in 1 country79 target enrollmentOctober 2006

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Diabetes Mellitus
Sponsor
The Catholic University of Korea
Enrollment
79
Locations
1
Primary Endpoint
physicians' labour time and frequency of contact with the online communication system required for reviewing the patients' information and sending recommendations
Status
Completed
Last Updated
16 years ago

Overview

Brief Summary

Background

  • Various kinds of interactive online communication systems have been introduced for long-term diabetes management, and their importance in managing patients is increasing. The investigators investigated the amount of physician time needed to maintain such a system, and the investigators developed software to maximise the cost effectiveness.

Methods

  • The investigators conducted a prospective, randomised, controlled trial to investigate the efficacy and safety of a semi-automatic response system (SARS) for online glucose monitoring over a 24-week period of patients with type 2 diabetes. In the SARS group, the "SARS" software filtered the recorded self-monitoring of blood glucose data automatically to reduce the physicians' time, and the physicians managed patients regularly but only manually in the control (manual) group. The investigators measured the time spent by the physicians for online management and compared the HbA1c levels at enrolment and follow-up.
Registry
clinicaltrials.gov
Start Date
October 2006
End Date
May 2007
Last Updated
16 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • men or women aged 20-70 years with type 2 diabetes
  • lasting more than one year who had used the online communication system for diabetes management at the web site https://www.bi odang.com for more than six months
  • baseline HbA1c level was 6-10%
  • Patients who able and willing to complete glucose-monitoring diaries on a web chart as instructed.

Exclusion Criteria

  • patients who required intensive insulin therapy (multiple insulin injections or insulin pump therapy) or who were unwilling to use self-monitoring of blood glucose (SMBG)
  • acute metabolic complications of diabetes (e.g., diabetic ketoacidosis, hyperosmolar non-ketotic hyperglycaemia, lactic acidosis)
  • serum creatinine concentration \>2.0 mg/dl at screening
  • active liver disease or ALT or AST activities \>2.5 times the upper limit of normal
  • acute illness, chronic infection, heart failure of NYHA Class III or IV
  • recent myocardial infarction or stroke during the past six months
  • pregnancy or GDM, or any other factor likely to limit protocol compliance or reporting of adverse events

Outcomes

Primary Outcomes

physicians' labour time and frequency of contact with the online communication system required for reviewing the patients' information and sending recommendations

Time Frame: 24 weeks

Study Sites (1)

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