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| Name | Class |
|---|---|
| University of Warwick | OTHER |
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This protocol concerns the implementation and evaluation of an intervention designed to realign the existing cadre of Community Health Workers (CHW) in Neno District, Malawi to better support the care needs of the clients they serve. The proposed intervention is a 'Household Model' where CHWs will be assigned to households, rather than HIV or TB specific patients, and will be trained to provide support for a wider range of conditions including HIV, hypertension, diabetes, and pediatric malnutrition. The new model is designed to improve retention in care for clients with chronic, non-communicable diseases, along with increased uptake of women's health services and treatment for pediatric malnutrition, while sustaining the high retention rates for clients in the HIV program. Eleven sites (health centres and hospitals) were arranged into six clusters by estimated size of the catchment area populations, with a population range of 11,680 to 26,260 and an average population of 20,400. The order in which the intervention will be rolled out across the sites will be randomized so that the intervention can be evaluated in a stepped-wedge cluster randomized controlled trial. These clusters were grouped based mostly on geographic location but also on catchment area sizes, in order to maximize feasibility of training for the CHW team and not overload CHW training sessions with too many trainees.
The objectives of the household model program are:
All CHWs in Neno will be reassigned and trained in the Household model in a staggered rollout over two years. The maximum number of trainees per group is capped at 60 participants, with some trainings occurring with two groups of CHWs per catchment area. CHWs will receive a 4 to 5 day foundational training, followed by half-day refresher trainings each quarter. CHW training will be evaluated through the following tools: training attendance count; CHW knowledge assessment; CHW skill assessment; CHW refresher assessment; and overall through a training dashboard.
The implementation of the new CHW model is designed so that it may be evaluated as a stepped wedge, cluster-randomized trial (SW-CRT). The stepped-wedge study design was selected for a number of reasons. First, the training of CHWs needs to be staggered due to training capacity constraints. Second, all sites in Neno will receive the intervention. And third, the stepped wedge RCT design permits estimation of the causal effects of the intervention.
Eleven intervention sites were clustered into six groups based on population size such that each group had manageable number of CHWs to train. The order of implementation for these six sites was randomized by a third party. In the SW-CRT study design, each cluster crosses over from control to intervention group until all groups receive the intervention.
The primary outcomes are:
HIV: % of enrolled clients with a visit to IC3 in the last 3m
NCDs
Malnutrition: % of children under five enrolled in care for moderate and severe pediatric malnutrition
Tuberculosis: % of total population diagnosed with new confirmed TB cases
Women's Health:
o Family Planning: % WCBA on long-term family planning methods
% women starting ANC within first trimester
The secondary outcomes are:
HIV:
Malnutrition:
o % of children aged 6m-59 who were discharged as cured in SFP or OTP (cure rate)
Tuberculosis:
Women's Health:
% women of child bearing age receiving modern family planning methods
% women of child bearing age newly initiating family planning
o Antenatal Care:
% expected pregnant women in ANC care
% number of women in cohort attending 4+ ANC visits
CHW retention o % of CHW retained during the entire intervention period
Descriptive Statistics:
Measure of Facility Performance o % of facilities offering women's health services on a daily basis
Outcomes Data
To measure the outcomes listed above, we will collect data from:
The study is designed as a stepped wedge randomized controlled trial. However, unlike a typical trial of this type, data will be collected at the aggregate cluster level rather than from individuals within clusters. As such, we specify a model for the cluster-time cell means. In addition, the primary outcomes are proportions of people, therefore we will specify the model in logs and control for population size to transform to the whole real line and make a linear model appropriate.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Zalewa | Active Comparator | Household Model Intervention introduced first - March 2017 |
|
| Ligowe and Magaleta | Active Comparator | Household Model Intervention to be introduced in June 2017 |
|
| Neno District Hospital and Neno Parish | Active Comparator | Household Model Intervention to be introduced in September 2017 |
|
| Matope | Active Comparator | Household Model Intervention to be introduced in December 2017 |
|
| Matandani and Nsambe | Active Comparator | Household Model Intervention to be introduced in March 2018 |
|
| Luwani, Nkula, and Midzemba | Active Comparator | Household Model Intervention to be introduced in June 2018 |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Household model | Behavioral | The proposed intervention is a 'Household Model' where, instead of being assigned to HIV or TB patients, CHWs will rather be assigned to households and will be trained to provide support for a wider range of conditions including HIV, hypertension, diabetes and pediatric malnutrition. The new model is designed to improve retention in care for clients with chronic, non-communicable diseases, along with increased uptake of women's health services and treatment for pediatric malnutrition, while sustaining the high retention rates for clients in the HIV program. |
| Measure | Description | Time Frame |
|---|---|---|
| HIV | Percentage of enrolled patients with a visit to integrated care clinic | Last 3 months |
| Hypertension | Percentage of enrolled patients with a visit to integrated care clinic | Last 3 months |
| Asthma | Percentage of enrolled patients with a visit to integrated care clinic | Last 3 months |
| Diabetes | Percentage of enrolled patients with a visit to integrated care clinic | Last 3 months |
| Epilepsy | Percentage of enrolled patients with a visit to integrated care clinic | Last 3 months |
| Mental Health | Percentage of enrolled patients with a visit to integrated care clinic | Last 3 months |
| Malnutrition | Percentage of children under five enrolled in care for moderate and severe paediatric malnutrition | Last 3 months |
| Tuberculosis | Percentage of total population diagnosed with new confirmed TB cases | Last 3 months |
| Measure | Description | Time Frame |
|---|---|---|
| ART Initiation | Percentage of clients initiated on ART with visit in last 3 months | Last year |
| EID | Percentage of infants who attend 10 week EID visit |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Luckson Dullie, MBBS, M Fam Med | Partners in Health | Principal Investigator |
| Elizabeth Dunbar, MPH | Partners in Health | Principal Investigator |
| Emily Wroe, MD, MPH | Partners in Health | Study Chair |
| Richard Lilford, Dsc, PhD, FRCOG, FRCP, FFPH | University of Warwick | Study Chair |
| Celia Taylor, BSocSc (Hons), PhD, QTS, FHEA | University of Warwick | Study Chair |
| Samuel Watson, PhD, MPH | University of Warwick | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Partners In Health / Abwenzi Pa Za Umoyo | Neno | Malawi |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 30007924 | Derived | Dunbar EL, Wroe EB, Nhlema B, Kachimanga C, Gupta R, Taylor C, Michaelis A, Cundale K, Dullie L, Jumbe A, Nazimera L, McBain R, Lilford RJ, Watson SI. Evaluating the impact of a community health worker programme on non-communicable disease, malnutrition, tuberculosis, family planning and antenatal care in Neno, Malawi: protocol for a stepped-wedge, cluster randomised controlled trial. BMJ Open. 2018 Jul 13;8(7):e019473. doi: 10.1136/bmjopen-2017-019473. |
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| ID | Term |
|---|---|
| D000163 | Acquired Immunodeficiency Syndrome |
| D006973 | Hypertension |
| D001249 | Asthma |
| D003920 | Diabetes Mellitus |
| D004827 | Epilepsy |
| D001523 | Mental Disorders |
| D044342 | Malnutrition |
| D014376 | Tuberculosis |
| ID | Term |
|---|---|
| D015658 | HIV Infections |
| D000086982 | Blood-Borne Infections |
| D003141 | Communicable Diseases |
| D007239 | Infections |
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The roll-out of this study is designed as a stepped wedge cluster randomised controlled trial. The study consists of six clusters: the first cluster will receive the intervention in March 2017, with a new cluster receiving the intervention every three months thereafter.
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|
| Family Planning |
Percentage of women of childbearing age on long-term family planning methods |
| Last 3 months |
| Antenatal Care | Percentage of women starting ANC within first trimester | Last 3 months |
| Last 3 months |
| HTC | Percentage of population tested for HIV | Last 3 months |
| Malnutrition - Cured | Percentage of children aged 6-59m who were discharged as cured in SFP or OTP (cure rate) | Last 3 months |
| Tuberculosis Treatment | Percentage of TB cases completing treatment successfully (no loss to follow up or death) | Last 3 months |
| Modern Family Planning Methods | Percentage of WCBA receiving modern family planning methods | Last 3 months |
| Newly Initiated Family Planning | Percentage of WCBA newly initiating family planning | Last 3 months |
| ANC Coverage | Percentage of expected pregnant women in ANC care | Last 3 months |
| 4+ ANC Visits | Percentage of in cohort attending 4+ ANC visits | Last 3 months |
| CHW Retention | Percentage of CHWs retained during the entire intervention period | Last 2 years |
| D015229 |
| Sexually Transmitted Diseases, Viral |
| D012749 | Sexually Transmitted Diseases |
| D016180 | Lentivirus Infections |
| D012192 | Retroviridae Infections |
| D012327 | RNA Virus Infections |
| D014777 | Virus Diseases |
| D012897 | Slow Virus Diseases |
| D000091662 | Genital Diseases |
| D000091642 | Urogenital Diseases |
| D007153 | Immunologic Deficiency Syndromes |
| D007154 | Immune System Diseases |
| D014652 | Vascular Diseases |
| D002318 | Cardiovascular Diseases |
| D001982 | Bronchial Diseases |
| D012140 | Respiratory Tract Diseases |
| D008173 | Lung Diseases, Obstructive |
| D008171 | Lung Diseases |
| D012130 | Respiratory Hypersensitivity |
| D006969 | Hypersensitivity, Immediate |
| D006967 | Hypersensitivity |
| D044882 | Glucose Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
| D004700 | Endocrine System Diseases |
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
| D009422 | Nervous System Diseases |
| D009748 | Nutrition Disorders |
| D009164 | Mycobacterium Infections |
| D000193 | Actinomycetales Infections |
| D016908 | Gram-Positive Bacterial Infections |
| D001424 | Bacterial Infections |
| D001423 | Bacterial Infections and Mycoses |