Lowering Blood Pressure by Changing Lifestyle (LBP)
High Blood Pressure

About this trial
This is an interventional health services research trial for High Blood Pressure focused on measuring lifestyle, health literacy, cluster RCT, physical exercise, smoking
Eligibility Criteria
Inclusion Criteria:
- Participants with clinic blood pressure more than or equal to 130/80 mm Hg who are not taking medication
- Participants with controlled blood pressure defined as < 130/80 using anti-hypertensive medication for a minimum of six weeks.
- Participants live in Banshgram Union only
Exclusion Criteria:
- Aged > 75 years of age
- Pregnant women
- People who have advanced CVDs or are any serious condition that restricts their participation in the study
- Participants will be withdrawn from the study if they are unwilling to continue their participation and withdraw their consent, or any women participants who become pregnant during the study.
Sites / Locations
- Organisation for Rural Community DevelopmentRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Monitoring of lifestyle change activities
lifestyle change activities: non-monitoring
The intervention arm will involve (i) the delivery of a blended learning education program and (ii) weekly phone calls to participants. The lectures will be delivered to 10 teams, comprised of about 15 participants in each team and lead by a volunteer team leader using the ORCD's laptop, overhead projector and the sound system in local clubs, school premises or participants' houses. The ORCD investigator including the physician and an information technology person will facilitate the education programs. The interpretations or additional explanations will be made by the physician following WHO guidelines and recommendations[36]. The investigator will maintain a folder for each team and will communicate at least with the team leaders by phone calls once every week to remind them to adhere to lifestyle modification intervention program. The weekly monitoring program will continue until the study ends.
The control group will only receive the printed materials, no active monitoring