The Application of the E-health Education on Shared Care Program for Patients With Type 2 Diabetes
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|ClinicalTrials.gov Identifier: NCT03061266|
Recruitment Status : Recruiting
First Posted : February 23, 2017
Last Update Posted : February 23, 2017
|Condition or disease||Intervention/treatment||Phase|
|Type 2 Diabetes Mellitus||Behavioral: E-health Education Other: Routine care||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||110 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Double (Participant, Investigator)|
|Primary Purpose:||Health Services Research|
|Official Title:||The Application of the E-health Education on Shared Care Program for Patients With Type 2 Diabetes - Taking Local Teaching Hospital for Example|
|Actual Study Start Date :||March 9, 2016|
|Estimated Primary Completion Date :||March 8, 2017|
|Estimated Study Completion Date :||March 8, 2017|
Experimental: E-health education group
E-health education group will be received the shared care program using e-health education.
Behavioral: E-health Education
E-health education on shared care program will be established by different type's professionals including diabetes physicians, pharmacists, dietitians and diabetes health teacher.
Control group will be received the shared care program as advised by clinical professionals, which included medications, dietary control and general physical activities.
Other: Routine care
Routine care on shared care program as advised by clinical professionals, which included medications, dietary control and general physical activities.
- Glycated hemoglobin (HbA1c) [ Time Frame: up to 6 months after the experiment ]glucose index
- Perceived diabetes self-management abilty using questionnaire [ Time Frame: baseline, 3 and 6 months after the experiment ]self-management abilty
- quality of life using questionnaire [ Time Frame: baseline, 3 and 6 months after the experiment ]the general well-being of individuals and societies, outlining negative and positive features of life
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): NCT03061266
|Contact: Chen Li-Li, PhDfirstname.lastname@example.org|
|Contact: Pai Lee-Wen, PhDemail@example.com|
|Puli Christian Hospital||Recruiting|
|Nantou, Taiwan, 54510|
|Contact: Chen Mei-Chih +886--49291-2151 firstname.lastname@example.org|
|Study Director:||Chen Li-Li, PhD||China Medical University, Taichung, Taiwan|
|Principal Investigator:||Pai Lee-Wen, PhD||Department of Nursing, Central Taiwan University of Science and Technology, Taichung, Taiwan|