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Clinical Trials/NCT02456064
NCT02456064
Completed
N/A

Impact of a Program of Non-pharmacological Intervention in Patients With Type 2 Diabetes Mellitus With Poor Control of Their Disease

Equipo Multidisciplinar Sanitario CS Foietes0 sites25 target enrollmentMay 2015

Overview

Phase
N/A
Intervention
Not specified
Conditions
Diabetes Mellitus, Type 2
Sponsor
Equipo Multidisciplinar Sanitario CS Foietes
Enrollment
25
Primary Endpoint
HbA1c
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this study is to determine whether a non-drug intensive program can help improve control of type 2 diabetes mellitus.

Detailed Description

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 .

Registry
clinicaltrials.gov
Start Date
May 2015
End Date
January 2016
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Equipo Multidisciplinar Sanitario CS Foietes
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients with type 2 diabetes mellitus with poor control of their disease.
  • No changes have been made in pharmacological previous 3 months.

Exclusion Criteria

  • Changes in their drug treatment in the past 3 months.

Outcomes

Primary Outcomes

HbA1c

Time Frame: 6 months

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