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NCT04191902 Clinical Trial

Educational Intervention Using SMS to Evaluate Clinical Effects and Satisfaction in Patients With Diabetes Mellitus

Educational Problems Clinical Trial

— SMS  

Official title:
Educational Intervention Using SMS to Evaluate Clinical Effects and Satisfaction in Patients With Diabetes Mellitus: A Brazilian Case Study

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT04191902
Other study ID # Diabetes Mellitus
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date January 5, 2021
Est. completion date February 15, 2022

Study information
Verified date November 2020
Source Universidade Federal Fluminense
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The investigators evaluated the satisfaction of these patients with the health service and their self-care. The study included patients diagnosed with DM, respecting the established inclusion and exclusion criteria. Participants were randomized into the control group and the intervention group.

Description:

Patients with diabetes mellitus (DM) have greater control over the disease when they acquire some knowledge about it. In this context, the use of technology by health professionals for nutritional guidance and self-care has shown promising results. This study aims to evaluate the impact of these educational approaches via SMS on glycemic control of patients with DM, followed at the Endocrinology Outpatient Clinic of the Antonio Pedro University Hospital (HUAP). Also, the investigators evaluated the satisfaction of these patients with the health service and their self-care. The study included patients diagnosed with DM, respecting the established inclusion and exclusion criteria. Participants were randomized into the control group and the intervention group. The patients in the intervention group received weekly SMS for six months, with dietary guidelines and DM care. Both groups answered a questionnaire at the beginning and end of the intervention, which consisted of assessing satisfaction with the health service received and their care for DM. Similarly, the investigators collected their clinical and laboratory data from medical records at the beginning and end of the intervention.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 50
Est. completion date February 15, 2022
Est. primary completion date January 5, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - diabetes Exclusion Criteria: - non diabetes

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• orientation
patients will be oriented

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Universidade Federal Fluminense

Outcome
Type Measure Description Time frame Safety issue
Primary differences in glycemic control Evaluation of the glycemic indices 1 year
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