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Evaluation of an Intervention Based on Cell Phones

Evaluation of the Effect of an Intervention Based on Cell Phones on Glycemic Control in Adults With Type 2 Diabetes Mellitus

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02094846
Enrollment
88
Registered
2014-03-24
Start date
2012-10-31
Completion date
2013-05-31
Last updated
2014-03-24

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

Conditions

Type 2 Diabetes Mellitus

Keywords

Cellular phones, Type 2 diabetes, Glycated hemoglobin, glycemic control

Brief summary

The aim of the study was to assess the effect of an individualized intervention based on cell phones to improve glycemic control in patients with type 2 diabetes attending Epidemiology Research Unit in Cuernavaca, Morelos. Mexico

Detailed description

In this study before randomization, the participants received workshops on diet, physical activity, glycemic index of foods. Bandura´s theoretical model was used in the voice messages sent to the intervention group.

Interventions

BEHAVIORALVoice messages

Voice messages reinforced with self-efficacy

Sponsors

Instituto Nacional de Salud Publica, Mexico
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
30 Years to 69 Years
Healthy volunteers
No

Inclusion criteria

* type 2 diabetes mellitus \> 10 years * Glycated hemoglobin \>7%

Exclusion criteria

* Take insulin regularly * Pregnant woman * Woman who expected to be pregnant the next 6 months * 24 hrs creatinine \< 30 ml/minute

Design outcomes

Primary

MeasureTime frameDescription
Glycated hemoglobinBasal and 3 monthsGlycated hemoglobin is obtained from a blood sample at the beginning of the study and 3 months later.

Secondary

MeasureTime frameDescription
Low Density LipoproteinBasal and 3 monthsLow Density Lipoprotein is obtained from a blood sample at the beginning of the study and 3 months later.
High Density LipoproteinBasal and 3 monthsHigh Density Lipoprotein is obtained from a blood sample at the beginning of the study and 3 months later.
CholesterolBasal and 3 monthsCholesterol is obtained from a blood sample at the beginning of the study and 3 months later.
Self-efficacyBasal and 3 monthsSelf-efficacy questionnaire is divided into a diet´s self-efficacy questionnaire and physical activity´s self-efficacy questionnaire. People can obtained low self-efficacy status or high self-efficacy status
Physical activityBasal and 3 monthsA triaxial accelerometer was used, colocated on the hip and the participants were supposed to use it 7 days for a minimal of 10 hours per day

Countries

Mexico

Outcome results

None listed

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