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Primary Care in the post-COVID-19 pandemic period: development of a Mobile Health Applicatio

Not Applicable
Recruiting
Conditions
Arterial Hypertension
Diabetes Mellitus
C23.550.291.898
Registration Number
RBR-45hqzmf
Lead Sponsor
niversidade Federal de Viçosa
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
Not specified
Inclusion Criteria

Age equal to or greater than 18 years; users of the Unified Health System (SUS); diagnosis of Arterial Hypertension (AH) and/or Diabetes Mellitus (DM); accompanied by the Family Health Strategy (ESF) teams

Exclusion Criteria

Age less than 18 years old; individuals with serious medical conditions; pregnant women; smoking volunteers; history of alcohol or drug abuse; bedridden; wheelchair users

Study & Design

Study Type
Intervention
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
It was expected to find a reduction in the clinical values of glycated hemoglobin in 6 months after the intervention, verified through the performance of biochemical tests and from the verification of a variation of at least 10% in the pre- and post-intervention measurements.;It was expected to find a reduction in blood pressure levels 6 months after the intervention, verified by measuring blood pressure and from the observation of a variation of at least 10% in pre- and post-intervention measurements.
Secondary Outcome Measures
NameTimeMethod
Evaluate the changes in anthropometric measurements (body weight, abdominal and calf circumference) in 6 months after the intervention, which will be verified with the aid of a scale and a body measuring tape and from the verification of a variation of at least 5 % in pre- and post-intervention measures.
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