This study aims to know the effectiveness of "MaRiTensi" in improving knowledge, motivation, efficacy, self-care and blood pressure control for hypertension patients.
This study hypothesizes that MaRiTensi effectively increases the knowledge, motivation, self-efficacy and self-care of hypertensive patients and reduces blood pressure in the intervention group compared to the control group.
Respondent recruitment is as follows:
1. The respondent candidate will be identified based on data on record medical
2. Appropriate respondent candidates' criteria inclusion and exclusion contacted for given informed consent
3. Prospective respondents who are willing to participate and fulfill the criteria for pressure blood moment measurement will request signed consent
4. Respondents fill in the basic data and recapitulate by the assistant researcher
5. Done randomization for allocation of group interventions and group control
6. Respondents given envelope closed (using sequentially numbered, opaque sealed envelopes (SNOSE) method )
7. Respondents' group intervention was given maintenance by Hospital or health center standard-added intervention using MaRiTensi by conditions; meanwhile, group control was provided care by Hospital or health center standards.