The purpose of this study is to determine whether a non-drug intensive program can help improve control of type 2 diabetes mellitus.
This study is based on the creation of two groups of patients with type 2 diabetes mellitus over a period of six months . In one of the groups an intensive program be developed through : group medical consultations , workshops , informative talks, " expert patient " telephone inquiries .. etc. Meanwhile , the control group that will be followed in the consultations as usual. We will make a determination of HbA1c at 3 months and 6 months later to assess whether there are significant differences between the two groups .
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
25
* Group medical visits * Telephone medical consultations * Expert patient * Training workshops
HbA1c
Time frame: 6 months
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