The Effect of Online Based Mentoring Program on the Blood Glucose and Satisfaction Score in Type 1 Diabetes Patients
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|ClinicalTrials.gov Identifier: NCT01157611|
Recruitment Status : Completed
First Posted : July 7, 2010
Last Update Posted : November 17, 2015
To evaluate the effects of online based mentoring program on the blood glucose and satisfaction score in type 1 diabetes patients. Peer group mentoring will be as effective as guidance by the doctors.
80 type 1 patients will be randomly divided into two groups (e.g. mentoring program group and control group). All patients will receive routine check up and blood test for ordinary type 1 patients. In addition, program group patients should register their SMBG, exercise, food intake and insulin dose on the website designed for this study and receive advices of mentors from peer group. Every patient will submit questionnaire on the first day of the study and the last day(after 12 weeks) of the study.
|Condition or disease||Intervention/treatment||Phase|
|Type 1 Diabetes||Behavioral: Mentoring program||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||57 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||The Effect of Online Based Mentoring Program on the Blood Glucose and Satisfaction Score in Type 1 Diabetes Patients|
|Study Start Date :||July 2010|
|Actual Primary Completion Date :||August 2013|
|Actual Study Completion Date :||August 2013|
Active Comparator: Mentoring program group
type 1 diabetes patients participating in online base mentoring program
Behavioral: Mentoring program
mentoring program group patients should register their SMBG, exercise, food intake and insulin dose on the website designed for this study and receive advices of mentors from peer group.
Other Name: online based mentoring program
No Intervention: Control group
type 1 diabetes patients receiving regular clinic visits
- change of the blood glucose [ Time Frame: week 0 (baseline), 6, 12 ]HbA1c, Fructosamine
- satisfaction score [ Time Frame: week 0 (baseline), 6, 12 ]incidence of hypoglycemia, numbers of daily SMBG, DTSQs, DTSQc, ADDQoL
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01157611
|Korea, Republic of|
|Samsung Medical Center|
|Seoul, Korea, Republic of, 135-710|
|Study Director:||Jae Hyeon Kim, M.D., Ph. D.||Samsung Medical Center|