diabetes
Conditions
Interventions
1:Intensive intervention plus conventional intervention
Sponsors
Third Military Medical University
Eligibility
Sex/Gender
All
Age
25 Years to 70 Years
Inclusion criteria
Inclusion criteria: Subjects were included if they (1) freely given informed consent; (2) had been identified within the last 6 months with pre-diabetes which is defined as a fasting plasma glucose level of 6.1mmol/L to 6.9mmol/L or a 2h plasma glucose of 7.8mmol/L to 11.0mmol/L after 75 grams glucose load; (3) age 25 to 60 years; (4) were accessible by mobile phone that could receive Chinese text message or micro letter; and (5) provided a family volunteer and a friend to support them in behaviour change.
Exclusion criteria
Exclusion criteria: Subjects were excluded from the study if they (1) had a history of diabetes mellitus; (2) unable to use mobile phone; (3) had major illness,such as cancer, chronic liver or kidney disease; (4) in pregnant or lactation period or plan to become pregnant during study; (5) another household member is a staff member in the study; (6) current or anticipated participation in another intervention research project that would interfere with any of the interventions offered in this trial; (7) were currently on medication known to alter glucose tolerance; and (8) conditions not specifically mentioned above may serve as criteria for exclusion at the discretion of the clinic site.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Blood glucose level test;blood pressure;Hemoglobin A1C; | — |
Secondary
| Measure | Time frame |
|---|---|
| Triglyceride;total cholesterol;high density lipoprotein cholesterol;Low high lipoprotein cholesterol;Weight;waist circumference; | — |
Countries
China
Contacts
Public ContactXiong Hongyan
Outcome results
None listed