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Integrated NCD Intervention in Rural Nepal

An Integrated Intervention for Chronic Care Management in Rural Nepal: a Type 2 Hybrid Effectiveness-implementation Study

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04087369
Enrollment
0
Registered
2019-09-12
Start date
2019-12-01
Completion date
2023-12-31
Last updated
2021-06-25

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

Conditions

Chronic Obstructive Pulmonary Disease, Diabetes Mellitus, Type 2, Hypertension, Noncommunicable Diseases

Keywords

implementation research, low- and middle-income countries, Nepal, Package of Essential Noncommunicable disease interventions for primary care in low-resource settings, task-shifting, non-physician health workers, digital tools, motivational interviewing

Brief summary

We will test an NCD intervention bundle incorporating the World Health Organisation (WHO)'s Package for Essential Non-Communicable Disease Interventions (PEN) within an approximate population of 300,000 people in rural Nepal. This intervention integrates three evidence-based approaches for both facility- and community-based NCD care focused on the key areas of Clinical Practice, Counseling, and Technology for two tiers of non-physician healthcare worker - Mid-Level Providers and Community Health Workers: 1) Task-shifting of evidence-based medicine algorithms and clinical skills from PEN protocols to non-physician healthcare workers; 2) Delivering quality counseling based on the Motivational Interviewing Model to drive behavior change with respect to both treatment adherence (defined as medication adherence and follow-up completion) and risk factor modification (alcohol, tobacco, diet, physical activity); 3) Employing a facility- and community-based clinical decision support tool for effective integration of PEN protocols into non-physician healthcare worker workflow. This five-year study will initial test the acceptability and feasibility of the intervention (two years) followed by a type 2 hybrid effectiveness-implementation research trial (three years) to which we will apply the RE-AIM implementation evaluative framework of both outcomes and process indicators. Co-primary outcomes for the intervention bundle will be: a) disease-specific, evidence-based control metrics that measures clinical efficacy; b) qualitative evaluation of acceptability and feasibility that incorporates perspectives of patients, providers, and government stakeholders; and c) an implementation checklist of key intervention process measures.

Interventions

OTHERBundled NCD WHO PEN Intervention

In the intervention includes the planned roll-out of the World Health Organization's Package of essential noncommunicable disease interventions (WHO PEN) for primary care in low resource settings by the Government of Nepal, Ministry of Health and Population. In addition, this intervention will include three evidence-based components: 1) non-communicable disease (NCD) care integration using mid-level practitioners (MLPs) and community healthcare workers (CHWs); 2) clinical decision support (CDS) tools to ensure quality care in accordance with best practices; and 3) training and supervision of MLPs to provide motivational interviewing (MI) techniques for modifiable risk factor optimization, with a specific focus on tobacco and alcohol use.

Sponsors

Nyaya Health Nepal
CollaboratorUNKNOWN
Ministry of Health and Population, Nepal
CollaboratorOTHER_GOV
Possible
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

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

Inclusion criteria

1. Adult patients aged 18 or older that screen into Nyaya Health Nepal/Possible's chronic disease program for the following conditions: Hypertension, Type II Diabetes Mellitus, COPD, and Asthma OR 2. Adult patients aged 18 or older with end-organ pathology resulting from the aforementioned conditions including the following: Chronic Kidney Disease, Ischemic Heart Disease, Cerebrovascular Disease AND 3. Healthcare staff; mid-level providers serving at district/primary health center-level facility; community health workers serving village clusters, Nyaya Health Nepal/Possible and Government of Nepal/Ministry of Health and Population employees involved in study design, program implementation, data collection, or data analysis processes. * Note, study populations 1 and 2 must reside in either Achham or Dolakha (Nepal) districts. * Patients must have a noncommunicable note in electronic medical record system at least twice (indicating at least one follow-up visit) and must have minimum 12 weeks in between baseline/endline clinical measures (indicating patients have been followed up for at least 3 months and have 3 months of exposure to intervention). * Patients do not need to have been in study for all 3 years. Duration of exposure to intervention will depend on stepped implementation design. Patients may be identified at Bayalpata Hospital (Achham, Nepal) or Charikot Primary Health Center (Dolakha, Nepal) by facility clinicians. Community health workers can also identify hypertensive patients and refer them to the facility for diagnosis confirmation. Patient enrollment will not be restricted by economic status or caste. Patients will not be recruited exclusively to participate in the study but will undergo routine evaluations, entering the final diagnosis in electronic health record system, tracking progress at each patient contact, the frequency for which is determined by the clinician's recommendation per World Health Organization Package of Essential Noncommunicable disease intervention protocols and the patient's availability. Patients will receive longitudinal care via the community health workers at their homes and at the hospitals by mid-level providers and staff physicians. Their receipt of care is not contingent upon their enrollment in the study; they receive care per routine service delivery.

Exclusion criteria

1. Patients migrate from the study are before completion of any of the Package of Essential Noncommunicable disease interventions 2. Patients explicitly request exclusion from the study and decline to consent to the study.

Design outcomes

Primary

MeasureTime frameDescription
Type II diabetes mellitus control measure24 monthsPercentage of enrolled type II diabetes patients achieving at goal status, at the completion of the study period (type II diabetes mellitus: Hemoglobin A1c \< 7.5 OR fasting blood sugar \<130 mg/dL)
Hypertension control measure24 monthsPercentage of enrolled hypertension patients achieving at goal status, at the completion of the study period (hypertension: blood pressure \<130/80mm Hg or patient-tailored goal per risk stratification)
COPD control measure24 monthsPercentage of enrolled COPD patients achieving at goal status, at the completion of the study period (COPD: exacerbation status ≤1/3 Anthonisen criteria)

Secondary

MeasureTime frameDescription
Tobacco use24 monthsPercentage of enrolled NCD patients who were using tobacco at enrollment who are non-users or who have reduced by \>50% their tobacco intake, at the completion of the study period
Alcohol use24 monthsPercentage of enrolled NCD patients who were alcohol drinkers at enrollment who are non-drinkers or who have reduced by \>50% alcohol intake, at the completion of the study period

Other

MeasureTime frameDescription
Clinic visit coverage (Reach)1 monthPercentage of enrolled NCD patients having an MLP visit at the clinic, measured monthly according to the patients indicated to be seen that month based on protocol-based guidelines
Demographic, geographic barriers and facilitators24 monthsPercentage of enrolled NCD patients whose CHW has GPS-mapped their households, describing barriers/facilitators to individuals' access, and identifying contributors to variation/inequities
Loss to follow-up (Reach)24 monthsPercentage of patients, stratified by demographic data and NCD conditions, that are lost-to-follow-up after enrollment
Monthly patient touch-points (Effectiveness)1 monthNumber of monthly per-patient touch-points, including interactions by both MLPs and CHWs
Evidence-based hypertension management (Effectiveness)3 monthsPercentage of enrolled hypertension patients in accordance with evidence-based recommendations, as prescribed by clinical algorithms, assessed quarterly by EHR audits
Evidence-based diabetes management (Effectiveness)3 monthsPercentage of enrolled diabetes patients in accordance with evidence-based recommendations, as prescribed by clinical algorithms, assessed quarterly by EHR audits
Evidence-based COPD management (Effectiveness)3 monthsPercentage of enrolled COPD patients in accordance with evidence-based recommendations, as prescribed by clinical algorithms, assessed quarterly by EHR audits
Village cluster adoption (Adoption)24 monthsPercentage of intended village clusters receiving intervention
MLP training adoption (Adoption)24 monthsPercentage of MLPs trained in intervention implementation
Care integration (Implementation)1 monthPercentage of all NCD patients enrolled at the facilities seen by CHWs at home within first month
CHW supervision completion (Implementation)3 monthsPercentage of scheduled CHW supervision field visits completed, stratified by CHN and district
CHW supervision review meeting completion (Implementation)3 monthsPercentage of scheduled quarterly data review meetings held with CHWs and CHNs
CHW home visit completion (Implementation)3 monthsPercentage of enrolled NCD patients with 100% of algorithm-indicated home visits received
CHW home visit fidelity (Implementation)3 monthsPercentage of of topics included at each session as dictated by the condition-specific algorithms, assessed during the CHW supervision field visits by CHNs
MLP retention adoption (Adoption)24 monthsPercentage of of trained MLPs retained in their positions at the completion of the study period
Referral completion (Implementation)3 monthsPercentage of % of patients referred by CHWs seen by MLPs within the prescribed time window according to the clinical algorithms (e.g. 24hours, 72 hours, 1 week)
MLP supervision model (Implementation)3 monthsPercentage of enrolled NCD patients appropriately referred to see a physician by MLPs as indicated by the clinical algorithms, assessed during monthly physician supervision sessions
MLP visit fidelity (Implementation)1 monthPercentage of of enrolled NCD patients with 100% of algorithm-indicated facility visits received, assessed during monthly physician supervision sessions
Total intervention cost (Maintenance)24 monthsCost of each intervention component and total costs using the Joint Learning Network costing methodology
Intervention initiation costs (Maintenance)24 monthsPercentage breakdown of initial (one-time) costs for intervention (training, equipment, etc)
Intervention maintenance costs (Maintenance)24 monthsPercentage breakdown of maintenance (recurring) costs (on-going training, personnel, materials, and other)
Facility vs. community costs (Maintenance)24 monthsPercentage of costs of health care divided between facility level and community level
Geographic cost variation (Maintenance)24 monthsVariance in costs between village clusters and districts within the intervention catchment area
Out-of-pocket patient costs (Maintenance)24 monthsPercentage of costs of health care divided between facility level and community level
Integrated intervention cost-effectiveness analysis (Maintenance)24 monthsPre/post intervention marginal effectiveness for primary outcomes
Cost per unit patient (Maintenance)24 monthsIntervention cost per enrolled patient
Cost per capita (Maintenance)24 monthsIntervention cost per capita
Projected scale cost(Maintenance)24 monthsProjected cost to scale intervention nationally
Referral fidelity (Implementation)3 monthsPercentage of patients appropriately referred to MLP care as indicated by the clinical algorithms, assessed during the CHW supervision field visits by CHNs
Timely adoption (Adoption)24 monthsPercentage of intended village clusters rolling-out intervention within 3 months of schedule, according to local governance decisions to roll-out the intervention
CHW training adoption (Adoption)6 monthsPercentage of CHWs trained in intervention implementation within first six months
CHW retention adoption (Adoption)24 monthsPercentage of of trained CHWs retained in their positions at the completion of the study period
Home visit coverage (Reach)1 monthPercentage of enrolled NCD patients having a CHW home visit

Countries

Nepal

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 28, 2026