Recruitment

Recruitment Status
Not yet recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Adhesion
  • Blood Pressure
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: The participants will be randomized into 2 intervention groupsMasking: Single (Outcomes Assessor)Masking Description: blind research assistantPrimary Purpose: Screening

Participation Requirements

Age
Between 18 years and 65 years
Gender
Both males and females

Description

To evaluate treatment adherence and blood pressure reduction, through the HiperCross App, between two groups of hypertensive patients in a Hypertension Public Ambulatory in Porto Alegre. The investigators hope to identify better adherence to treatment, as well as a significant reduction in blood pre...

To evaluate treatment adherence and blood pressure reduction, through the HiperCross App, between two groups of hypertensive patients in a Hypertension Public Ambulatory in Porto Alegre. The investigators hope to identify better adherence to treatment, as well as a significant reduction in blood pressure, all of these results will be better evaluated using the HiperCross application.

Tracking Information

NCT #
NCT04475367
Collaborators
Not Provided
Investigators
Study Director: Bruna Eibel, PhD Post Graduation professor - Cardiology Foundation