Skip to content

Comprehensive Approach to Hypertension Management in Nepal

A Cluster Randomized Trial to Evaluate Comprehensive Approach to Hypertension Management in Nepal

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05292469
Enrollment
1252
Registered
2022-03-23
Start date
2022-05-02
Completion date
2023-08-29
Last updated
2025-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension

Keywords

Nepal, Monitoring

Brief summary

Hypertension is a global risk factor for cardiovascular diseases. Approximately 80% hypertension burden is in low-and-middle income countries. Hypertension can be managed with antihypertensive medication and following effective lifestyle interventions, however the control rate of hypertension among those on treatment is dismal. In Nepal, a quarter of adult population have hypertension of whom, 44% are unaware of their status, 33% are on treatment, and, only 12% are controlled. A comprehensive intervention strategy for hypertension management has shown promising results in high income countries. Therefore, it is of interest to understand its effectiveness, appropriateness and feasibility in the low income settings such as Nepal. The objective of the trial is to assess the impact on net change in mean systolic blood pressure measured between 7 to 8 months follow-up of a comprehensive intervention which provides personalized counselling on lifestyle modification and medication adherence together with support for regular monitoring of blood pressure at home, compared with a control arm where hypertensive patients have access to routine care only. The investigators are proposing a cluster randomized controlled trial conducted in government health facilities from Budhanilakantha, an urban municipality in the Bagmati Province of Nepal. Trial arms: 1) control (routine hypertension care); 2) Comprehensive approach to hypertension management that includes blood pressure (BP) audit and feedback by physician (nurse and doctor), and patient support to monitor BP, and home based patient care by community health workers to encourage self-monitoring of BP followed by tailored educational counselling on behavioral and lifestyle change. Eligible participants providing consent will be enrolled into the trial by a research assistant who will conduct interviews. Those from the intervention arm will receive the home visits for 6 months. Participants from both arms will provide follow up data in 7 to 8 months.

Interventions

BEHAVIORALComprehensive approach to hypertension management

Trained health workers will review blood pressure (BP) logs and provide treatment. The patients will receive a BP lowering informational package, BP monitoring device and log book and pill-box and medication table. The participants will receive monthly home visits (6 visits) to discuss hypertension and ways to manage it. They will be encouraged to identify problems and developing an action plan to solve them. The participants will be encouraged to set behavioral goals. The follow up visits will review the progress made in implementing action plan and goals set and updating them. Review BP logs and facilitate tailored discussion on topics based on problems faced by participants on barriers to medication adherence, physical activity, weight management or diet. The family members will be involved and be accountable in supporting the patients in achieving the action plans.

Sponsors

Institute for Implementation Sciences and Health, Kathmandu, Nepal
CollaboratorUNKNOWN
Norwegian University of Science and Technology
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

Cluster randomized Trial

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Hypertension patients (systolic blood pressure 140 mmHg or more and/or diastolic blood pressure 90 mmHg or more on at least two separate visits, or use of antihypertensive medication) * Living in the area served by the participating health facilities

Exclusion criteria

* Pregnancy * Not able or willing to give informed consent, * Critically ill from depilating conditions such as dialysis, cancer, palliative care * Not likely to continue living in the area served by the health facility during trial follow up period (8 months)

Design outcomes

Primary

MeasureTime frameDescription
Mean systolic blood pressure (BP) (mmHg)Measured at baseline and follow up between 7 to 8 months after baselineNet change in mean systolic BP from baseline to follow up

Secondary

MeasureTime frameDescription
Proportion controlling BP (<140/90 mmHg)Measured at baseline and follow up between 7 to 8 months after baselineProportion of participants controlling BP (\<140/90 mmHg) from baseline to follow up
Waist Circumference (cm)Measured at baseline and follow up between 7 to 8 months after baselineThe mean difference in waist circumference measured at baseline and follow up
Body weight (Kg)Measured at baseline and follow up between 7 to 8 months after baselineThe mean difference in weight measured at baseline and follow up
Diet low in cholesterol, high in fruits and vegetablesReported at baseline and follow up between 7 to 8 months after baselineThe proportion consuming diet low in cholesterol, high in fruits and vegetables in the last 24 hours self reported at baseline and follow up
Daily salt intake (<1 teaspoon per day)Reported at baseline and follow up between 7 to 8 months after baselineThe proportion consuming less than 1 teaspoon of salt per day self reported at baseline and follow up
Mean diastolic BP (mmHg)Measured at baseline and follow up between 7 to 8 months after baselineNet change in mean diastolic BP from baseline to follow up
Physical activitySelf reported at baseline and follow up between 7 to 8 months after baselineThe proportion engaged in moderate physical activity (2.5 hours per week) measured at baseline and follow up
Hypertension Knowledge ScoreSelf reported at baseline and follow up between 7 to 8 months after baselineAll together 21 hypertension knowledge statement with 12 true false responses and others with multiple responses to create a aggregate score on hypertension Knowledge
Perceived Social Support ScaleSelf reported at baseline and follow up between 7 to 8 months after baselineTwelve statements on perceived social support with 7 point Likert scale will be used at baseline and endline
Maintaining BP logsSelf reported at follow up between 7 to 8 months after baselineProportion of trial participants maintaining self BP measurement logs asked during follow up
Medication adherenceSelf reported at baseline and follow up between 7 to 8 months after baselineThe proportion adhering to prescribed medication in the past two weeks measured at baseline and follow up

Countries

Nepal

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 27, 2026