Diabetes mellitus
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients with diabetes mellitus treated with conventional insulin, attended by the Pharmacy of the Family Health Center of Fernandes Pinheiro; with cognitive ability; who agree to participate in the research by signing the Informed Consent Form.
Exclusion criteria
Exclusion criteria: Patients with cognitive difficulties who do not have a companion or caregiver, hindering the understanding of the pharmaceutical and study guidelines. Diabetes mellitus patients receiving insulin analogues or not receiving insulin treatment.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected Outcome 1. Improve treatment adherence by assessing the degree of agreement between the actual and estimated withdrawal intervals in days before and at the end of pharmacotherapeutic follow-up.;Expected Outcome 2. Improve glycemic control by reducing glycated hemoglobin from baseline. Data collected before the first intervention and at the 9th month, at the end of pharmacotherapeutic follow-up.;Expected Outcome 3. Improve patients' quality of life, according to the DQOL-Brazil-8 questionnaire, applied before and after pharmacotherapeutic follow-up. | — |
Secondary
| Measure | Time frame |
|---|---|
| Improve glycemic control by reducing fasting blood glucose levels and self-monitoring of blood glucose. Data collected at all stages of pharmacotherapeutic follow-up.;Reduce problems related to pharmacotherapy, according to an instrument of the Ministry of Health. Data collected at all stages of pharmacotherapeutic follow-up. | — |
Countries
Brazil
Contacts
Universidade Estadual de Ponta Grossa