The goal of this clinical trial is to evaluate whether a multifaceted community-based intervention, comprising 1) screening and lifestyle counseling by female community health volunteers (FCHVs); community health workers in Nepal, through home visits, and 2) regular Short Message Service (SMS) messages, can effectively reduce systolic blood pressure (SBP), lower fasting blood glucose, and increase smoking cessation rates among adults living in Pokhara with hypertension, type 2 diabetes, and smoking habits, respectively. The main research questions are: * Can FCHV home visits combined with regular mobile phone messages focused on blood pressure management reduce systolic blood pressure in adults with hypertension? * Can FCHV home visits combined with regular mobile phone messages focused on diabetes management lower fasting blood glucose levels in adults with type 2 diabetes? * Can FCHV home visits combined with regular mobile phone messages focused on smoking cessation increase the cessation rate among current smokers? Researchers will compare the intervention group with a usual care group, which does not receive regular FCHV home visits for managing the three aforementioned risk factors or mobile phone messages.
Background: Rapid globalization and urbanization continue to escalate the burden of non-communicable diseases (NCDs) across the world, disproportionally affecting low- and middle-income countries (LMICs). To date, trials have documented that task-sharing with community health workers (CHWs) can reduce systolic blood pressure and fasting blood glucose and achieve smoking cessation. However, most trials have been done in rural settings, and only focused on managing a single condition, such as hypertension. Furthermore, despite increasing evidence of the effectiveness from clinical trials, there is a lack of studies exploring best practices for 'how' to implement and sustain these interventions in LMICs. Study Design: Type 2 hybrid effectiveness-implementation research study containing 1) a qualitative study, 2) open-label, two-armed, cluster randomized controlled trial (cRCT), and 3) implementation research plan. The details of the c-RCT only are presented below. Settings: Pokhara Metropolitan City of Nepal. Pokhara is the second largest city in Nepal containing 33 administrative units called "wards". The investigators consider wards as clusters and randomize these 30 clusters (28 independent wards and 2 combined wards) into intervention and control groups in a 1:1 ratio. Participants: Adults with ages between 40-75 having at least one of the following conditions: * Hypertension, defined as: i. BP≥140/90 mmHg at two separate measures, or ii. Under pharmacotherapy for hypertension * Type 2 diabetes mellitus, defined as i. Fingerprick glucose (fasting) ≥100 mg/dl, plasma glucose (fasting) ≥126 mg/dL, and ii. HbA1c ≥ 6.5 %, or iii. Under pharmacotherapies for type 2 diabetes * Current tobacco smoking, defined as i. Ever smoked ≥100 cigarettes in lifetime, and ii. Currently smokes every day or on some days. Intervention: Multifaceted intervention containing the following two components: 1. FCHV home visits every three months 2. Mobile phone messages, including Control: Usual care in Pokhara Metropolitan City in Nepal, which does not include FCHV home visits for management of hypertension, diabetes, or smoking, and mobile phone messages. Outcome: Changes in systolic blood pressure, fasting blood glucose, and smoking cessation at 6 months post randomization will be measured as primary outcomes.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SCREENING
Masking
NONE
Enrollment
2,070
1. FCHV home visits every three months, including * For hypertension i. Blood pressure measurement with digital BP devices ii. Lifestyle counseling iii. Referral if uncontrolled BP (≥140/90 mmHg) for 3 months * For type 2 diabetes i. Fasting blood glucose measurement with glucometer ii. Lifestyle counseling focusing on diabetes management iii. Referral if uncontrolled diabetes (≥126mg/dl) for 3 months * For current smokers i. Smoking cessation counseling ii. Referral for nicotine replacement therapy if request by participants 2. Mobile phone messages, including * Lifestyle modification * Conveyed as voice or text messages, depending on participant preference
Pokhara Metropolitan City
Pokhara, Gandaki, Nepal
RECRUITINGSystolic blood pressure (mmHg)
Difference in systolic blood pressure change between the intervention and the control groups among participants enrolled as having hypertension.
Time frame: 6 months post randomization
Fasting Plasma glucose
Difference in fasting plasma glucose change between the intervention and the control groups among participants enrolled as having type 2 diabetes.
Time frame: 6 months post randomization
Participants Who Have Achieved Smoking cessation
Participants who have not smoked for the past 30 days between the intervention and the control groups, among participants enrolled as current smokers.
Time frame: 6 months post randomization
Diastolic blood pressure (mmHg)
Difference in diastolic blood pressure change between the intervention and the control groups among participants enrolled as having hypertension.
Time frame: 6 months post randomization
Controlled blood pressure control (<140/90 mmHg) rate
Difference in the proportion of those with BP\<140/90 mmHg between the intervention and the control groups, among participants enrolled as having hypertension.
Time frame: 6 months post randomization
Mean HbA1c level
Difference in mean HbA1c between the intervention and the control groups, among participants enrolled as having type 2 diabetes.
Time frame: 6 months post randomization
Mean Weight in Kg
Difference in mean weight between the intervention and the control groups, among participants enrolled as having type 2 diabetes.
Time frame: 6 months post randomization
Mean Total Cholesterol (mg/dL)
Difference in mean total cholesterol levels between the intervention and the control groups, among participants with high total cholesterol (≥ 200 mg/dL) at baseline.
Time frame: 6 months post randomization
Mean HDL (mg/dL)
Difference in mean HDL levels between the intervention and the control groups, among participants with low HDL (\< 40 mg/dL) at baseline.
Time frame: 6 months post randomization
Mean LDL level (mg/dL)
Difference in mean LDL levels between the intervention and the control groups, among participants with high LDL (≥ 100 mg/dL) at baseline.
Time frame: 6 months post randomization
Mean Triglyceride Levels (mg/dL)
Difference in mean triglyceride levels between the intervention and the control groups, among participants with high triglyceride level (≥ 150 mg/dL) at baseline.
Time frame: 6 months post randomization
Medication adherence, antihypertensive medicines
Difference in the proportion of those not missing a single anti-hypertensive pill over the past 1 week between the intervention and the control groups, among participants enrolled as having hypertension.
Time frame: 6 months post randomization
Medication adherence, hypoglycemic medicines
Difference in the proportion of those not missing a single hypoglycemic pill or injection over the past 1 week between the intervention and the control groups, among participants enrolled as having type 2 diabetes.
Time frame: 6 months post randomization
Fagerstrom Test for Nicotine Dependence (FTND) score
Difference in the proportion of those with a high FTND score (5-10) between the intervention and the control groups, among participants enrolled as current smokers. Higher means more dependence on nicotine.
Time frame: 6 months post randomization
Smoking cessation, 7 days
Difference in the proportion of those who have not smoked for the past 7 days between the intervention and the control groups, among participants enrolled as current smokers.
Time frame: 6 months post randomization
Harmful alcohol consumption rate, self-report
Difference in the proportion of those taking 7 (if women) and 14 (if men) standard drinks over the past 1 week between the intervention and the control groups, among all participants.
Time frame: 6 months post randomization
Low dietary salt intake rate, self-report
Difference in the proportion of those taking 5 mg or less salt per day between the intervention and the control groups, among participants enrolled as having hypertension.
Time frame: 6 months post randomization
High physical activity rate, self-report
Difference in the proportion of those who had 3000 metabolic equivalents of tasks (MET) or more per week between the intervention and control groups, among participants enrolled as having hypertension and/or diabetes.
Time frame: 6 months post randomization
High fruit and vegetable intake rate, self-report
Difference in the proportion of those who consumed 5 or more servings of fruits and/or vegetables per day between the intervention and control groups, among participants enrolled as having hypertension and/or diabetes.
Time frame: 6 months post randomization
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