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self-care economic evaluation of patients with type 2 diabetes mellitus

Pharmacotherapeutic strategy for individual empowerment of patients with diabetes mellitus type 2 - pharmacoeconomic analysis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-6t4qmn
Enrollment
Unknown
Registered
2016-09-23
Start date
2015-08-15
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 2 Diabetes Mellitus diabetes complications

Interventions

Group Intervention: Individual Empowerment pharmacotherapy (EIEF). 46 participants. Three meetings with the pharmaceutical, 1st meeting: presentation of the project, informed consent signature, applic
Identification of priority to be worked. After 30 days - 3 - selection of an activity, task or action to establish a goal. After 120 days it happens the 4th meeting to evaluate the results and guideli
Drug
Other
N03.219.390

Sponsors

Universidade Federal São João Del-Rei
Lead Sponsor
Universidade Federal São João Del-Rei
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Group Intervention: Patients with DM2 registered HIPERDIA. Aged 18 years. Both sexos.Residentes in the areas of coverage of ESFs belonging to the study. Graduates of EIEF. Low and moderate cardiovascular risk, according to the Framingham score. Control Group: Patients with DM2 registered HIPERDIA. Age less than 18. Both sexes. Residents in the areas covered by ESFs belonging to the study. No participant in any meeting of EIEF. Low and moderate cardiovascular risk, according to the Framingham score.

Exclusion criteria

Exclusion criteria: Group Intervention: Participants from other intervention projects related to DM. reduced cognitive ability, classified by the team of the FHS, as unable to reproduce the transferred information. Control Group:Indivíduos participants from other intervention projects related to DM. Patients with reduced cognitive ability, classified by the ESF team, as unable to reproduce the transferred information. Patients without result HbA1c in the reference period for data collection the study.

Design outcomes

Primary

MeasureTime frame
VVariation of 0.67 in mean glycated hemoglobin , comparing the beginning and end of the study , verified by conducting the laboratory examination .

Secondary

MeasureTime frame
Cost-effectiveness analysis : total annual cost of each group ( currency ) divided by the change in HbA1c ( observed benefit) , measured at the beginning and end of the intervention , through consultation of the computerized system (cost) and laboratory test (HbA1c );Reason Incremental Cost-Effectiveness : Cost difference between the intervention and control groups divided by the difference of change in HbA1c between the intervention and control groups, measured at the beginning and end of the intervention , through consultation of the computerized system (cost) and laboratory examination (HbA1c).;Markov modeling: Patients will be allocated according to the Markov health status (healthy, stable, blindness and death). Each of these branches node has a probability weight ranging between 0 and 1. It is then held Markov modeling ten cycles, each cycle corresponding to a year. Thus, you can estimate the number of patients who could develop any complications related to DM2 the end of ten years. The terminal node death will also be possible to estimate the number of years of life were saved by the intervention.

Countries

Brazil

Contacts

Public ContactAna Carolina Gonçalves

Universidade Federal São João Del-Rei

aco_goncalves@yahoo.com.br+55 (37) 99115 0193

Outcome results

None listed

Source: REBEC (via WHO ICTRP)