Primary Care in the post-COVID-19 pandemic period: development of a Mobile Health Applicatio
Not Applicable
Recruiting
- Conditions
- Arterial HypertensionDiabetes MellitusC23.550.291.898
- 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
Name Time Method 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
Name Time Method 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.