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Semi-automatic Response System(SARS)in Type 2 Diabetes

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01058733
Acronym
SARS
Enrollment
79
Registered
2010-01-29
Start date
2006-10-31
Completion date
2007-05-31
Last updated
2010-01-29

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

Conditions

Diabetes Mellitus

Keywords

semi-automatic response system (SARS), Diabetes Mellitus, Internet, ubiquitous health care system

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.

Interventions

new clinical decision-supporting system for glucose monitoring, SARS, which could identify glucose data recorded by patients and make some optimal decisions.The SARS engine assigned subjects to one of three levels according to the glucose control status and glucose control method.

Sponsors

The Catholic University of Korea
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 70 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frame
physicians' labour time and frequency of contact with the online communication system required for reviewing the patients' information and sending recommendations24 weeks

Countries

South Korea

Outcome results

None listed

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