Type 2 diabetes
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients with type 2 diabetes who have been taking 2 or more oral antidiabetic drugs for more than 3 months. The prescription time at the time of consent is 28 days or more. Men and women over the age of 18 when obtaining consent. Consent for study participation was obtained. Patients who meet all of the above.
Exclusion criteria
Exclusion criteria: Use of insulin injection, use of GLP-1 receptor agonist, home patient, dementia, diabetes completely cured during study period, hospitalized patient, drug management is third party, dialysis patient, lactating woman, alcohol / Drug addiction. Those who receive dietary guidance from a dietitian during the survey period. The above is excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Compare the DTR QOL of the intervention group and control group after 3 months with the baseline | — |
Secondary
| Measure | Time frame |
|---|---|
| HbA1c Copmare mean increase or decrease values of intervention group and control group Compliance and adherence Compare the mean number of days prescribed for the intervention group and the control group divided by the interval between visits. Remaining drug remaining drug amount Compare the baseline and difference of the intervention group and control group after 3 months. The price is calculated at the price determined by the Ministry of Health Labor and Welfare. Side effects sick days Compare the percentage of all phone calls in the intervention group that found side effects and sick days. Number of written reports to doctors Compare the number of written submissions in the intervention and control groups the number of drug changes and dose changes. Reduced drug Compared the increase and decrease in the number of drugs in the diabetes prescription of the intervention group and the control group. | — |
Countries
Japan
Contacts
Total Medical Service Co., Ltd. Sakura Pharmacy, Shingu Chuo Station