Impact of a Program of Non-pharmacological Intervention in Patients With Type 2 Diabetes Mellitus

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

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT02456064

Enrollment

Registered

2015-05-28

Start date

2015-05-31

Completion date

2016-01-31

Last updated

2017-03-28

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

Conditions

Diabetes Mellitus, Type 2

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 .

Interventions

BEHAVIORALLifestyle counseling

* Group medical visits * Telephone medical consultations * Expert patient * Training workshops

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

25 Years to No maximum

Healthy volunteers

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.

Design outcomes

Primary

Measure	Time frame
HbA1c	6 months

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026