Strengthening primary care for diabetes and hypertension in Eswatini: study protocol for a nationwide cluster-randomized controlled trial.

Cardiovascular disease Community health worker Community outreach Diabetes Differentiated service delivery Eswatini Health service decentralization Hypertension Non-communicable disease WHO-PEN

Journal

Trials
ISSN: 1745-6215
Titre abrégé: Trials
Pays: England
ID NLM: 101263253

Informations de publication

Date de publication:
22 Mar 2023
Historique:
received: 22 12 2022
accepted: 12 01 2023
entrez: 23 3 2023
pubmed: 24 3 2023
medline: 25 3 2023
Statut: epublish

Résumé

Diabetes and hypertension are increasingly important population health challenges in Eswatini. Prior to this project, healthcare for these conditions was primarily provided through physician-led teams at tertiary care facilities and accessed by only a small fraction of people living with diabetes or hypertension. This trial tests and evaluates two community-based healthcare service models implemented at the national level, which involve health care personnel at primary care facilities and utilize the country's public sector community health worker cadre (the rural health motivators [RHMs]) to help generate demand for care. This study is a cluster-randomized controlled trial with two treatment arms and one control arm. The unit of randomization is a primary healthcare facility along with all RHMs (and their corresponding service areas) assigned to the facility. A total of 84 primary healthcare facilities were randomized in a 1:1:1 ratio to the three study arms. The first treatment arm implements differentiated service delivery (DSD) models at the clinic and community levels with the objective of improving treatment uptake and adherence among clients with diabetes or hypertension. In the second treatment arm, community distribution points (CDPs), which previously targeted clients living with human immunodeficiency virus, extend their services to clients with diabetes or hypertension by allowing them to pick up medications and obtain routine nurse-led follow-up visits in their community rather than at the healthcare facility. In both treatment arms, RHMs visit households regularly, screen clients at risk, provide personalized counseling, and refer clients to either primary care clinics or the nearest CDP. In the control arm, primary care clinics provide diabetes and hypertension care services but without the involvement of RHMs and the implementation of DSD models or CDPs. The primary endpoints are mean glycated hemoglobin (HbA1c) and systolic blood pressure among adults aged 40 years and older living with diabetes or hypertension, respectively. These endpoints will be assessed through a household survey in the RHM service areas. In addition to the health impact evaluation, we will conduct studies on cost-effectiveness, syndemics, and the intervention's implementation processes. This study has the ambition to assist the Eswatini government in selecting the most effective delivery model for diabetes and hypertension care. The evidence generated with this national-level cluster-randomized controlled trial may also prove useful to policy makers in the wider Sub-Saharan African region. NCT04183413. Trial registration date: December 3, 2019.

Sections du résumé

BACKGROUND BACKGROUND
Diabetes and hypertension are increasingly important population health challenges in Eswatini. Prior to this project, healthcare for these conditions was primarily provided through physician-led teams at tertiary care facilities and accessed by only a small fraction of people living with diabetes or hypertension. This trial tests and evaluates two community-based healthcare service models implemented at the national level, which involve health care personnel at primary care facilities and utilize the country's public sector community health worker cadre (the rural health motivators [RHMs]) to help generate demand for care.
METHODS METHODS
This study is a cluster-randomized controlled trial with two treatment arms and one control arm. The unit of randomization is a primary healthcare facility along with all RHMs (and their corresponding service areas) assigned to the facility. A total of 84 primary healthcare facilities were randomized in a 1:1:1 ratio to the three study arms. The first treatment arm implements differentiated service delivery (DSD) models at the clinic and community levels with the objective of improving treatment uptake and adherence among clients with diabetes or hypertension. In the second treatment arm, community distribution points (CDPs), which previously targeted clients living with human immunodeficiency virus, extend their services to clients with diabetes or hypertension by allowing them to pick up medications and obtain routine nurse-led follow-up visits in their community rather than at the healthcare facility. In both treatment arms, RHMs visit households regularly, screen clients at risk, provide personalized counseling, and refer clients to either primary care clinics or the nearest CDP. In the control arm, primary care clinics provide diabetes and hypertension care services but without the involvement of RHMs and the implementation of DSD models or CDPs. The primary endpoints are mean glycated hemoglobin (HbA1c) and systolic blood pressure among adults aged 40 years and older living with diabetes or hypertension, respectively. These endpoints will be assessed through a household survey in the RHM service areas. In addition to the health impact evaluation, we will conduct studies on cost-effectiveness, syndemics, and the intervention's implementation processes.
DISCUSSION CONCLUSIONS
This study has the ambition to assist the Eswatini government in selecting the most effective delivery model for diabetes and hypertension care. The evidence generated with this national-level cluster-randomized controlled trial may also prove useful to policy makers in the wider Sub-Saharan African region.
TRIAL REGISTRATION BACKGROUND
NCT04183413. Trial registration date: December 3, 2019.

Identifiants

pubmed: 36949485
doi: 10.1186/s13063-023-07096-4
pii: 10.1186/s13063-023-07096-4
pmc: PMC10031170
doi:

Banques de données

ClinicalTrials.gov
['NCT04183413']

Types de publication

Clinical Trial Protocol Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

210

Subventions

Organisme : Horizon 2020
ID : 825823

Informations de copyright

© 2023. The Author(s).

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Auteurs

Michaela Theilmann (M)

Heidelberg Institute of Global Health, Heidelberg University, Im Neuenheimer Feld 130.3, 69120, Heidelberg, Germany. michaela.theilmann@uni-heidelberg.de.
Assistant Professorship of Behavioral Science for Disease Prevention and Health Care, Technical University of Munich, Munich, Germany. michaela.theilmann@uni-heidelberg.de.

Ntombifuthi Ginindza (N)

Ministry of Health in Eswatini, Ministry of Justice & Constitutional Affairs Building, Mhlambanyatsi Road, Mbabane, Eswatini.

John Myeni (J)

Ministry of Health in Eswatini, Ministry of Justice & Constitutional Affairs Building, Mhlambanyatsi Road, Mbabane, Eswatini.

Sijabulile Dlamini (S)

Ministry of Health in Eswatini, Ministry of Justice & Constitutional Affairs Building, Mhlambanyatsi Road, Mbabane, Eswatini.

Bongekile Thobekile Cindzi (BT)

Clinton Health Access Initiative, Mbhilibhi House, Plot 170, Corner Tsekwane/Mbhilibhi Street, Mbabane, Eswatini.

Dumezweni Dlamini (D)

Diabetes Eswatini, Manzini, Eswatini.

Thobile L Dlamini (TL)

Eswatini Business Health and Wellness, Malagwane Hill, Mbabane, Eswatini.

Maike Greve (M)

University of Göttingen, Humboldtallee 3, 37073, Göttingen, Germany.

Harsh Vivek Harkare (HV)

Swiss Tropical and Public Health Institute, Kreuzstrasse 2, 4123, Allschwil, Switzerland.
University of Basel, Basel, Switzerland.

Mbuso Hleta (M)

Eswatini Business Health and Wellness, Malagwane Hill, Mbabane, Eswatini.

Philile Khumalo (P)

Diabetes Eswatini, Manzini, Eswatini.

Lutz M Kolbe (LM)

University of Göttingen, Humboldtallee 3, 37073, Göttingen, Germany.

Simon Lewin (S)

Division of Health Services, Norwegian Institute of Public Health, Oslo, Norway.
Department of Health Sciences Ålesund, Norwegian University of Science and Technology (NTNU), Ålesund, Norway.
Health Systems Research Unit, South African Medical Research Council, Cape Town, South Africa.

Lisa-Rufaro Marowa (LR)

Clinton Health Access Initiative, Mbhilibhi House, Plot 170, Corner Tsekwane/Mbhilibhi Street, Mbabane, Eswatini.

Sakhile Masuku (S)

University of Eswatini, M48V+JXG, Mbabane, Eswatini.

Dumsile Mavuso (D)

Diabetes Eswatini, Manzini, Eswatini.

Marjan Molemans (M)

Amsterdam Institute for Global Health and Development, Paasheuvelweg 25, 1105 BP, Amsterdam, Netherlands.
Amsterdam Institute for Social Science Research, Amsterdam, Netherlands.
Amsterdam Public Health Research Institute, Amsterdam, Netherlands.

Nyasatu Ntshalintshali (N)

Clinton Health Access Initiative, Mbhilibhi House, Plot 170, Corner Tsekwane/Mbhilibhi Street, Mbabane, Eswatini.

Nomathemba Nxumalo (N)

University of Eswatini, M48V+JXG, Mbabane, Eswatini.

Brianna Osetinsky (B)

Swiss Tropical and Public Health Institute, Kreuzstrasse 2, 4123, Allschwil, Switzerland.
University of Basel, Basel, Switzerland.

Christopher Pell (C)

Amsterdam Institute for Global Health and Development, Paasheuvelweg 25, 1105 BP, Amsterdam, Netherlands.
Amsterdam Public Health Research Institute, Amsterdam, Netherlands.
Amsterdam UMC, location University of Amsterdam, Department of Global Health, Amsterdam, The Netherlands.

Ria Reis (R)

Amsterdam Institute for Global Health and Development, Paasheuvelweg 25, 1105 BP, Amsterdam, Netherlands.
Amsterdam Institute for Social Science Research, Amsterdam, Netherlands.
Dept. of Public Health & Primary Care, Leiden University Medical Center, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands.
School of Child and Adolescent Health, Children's Institute, University of Cape Town, Cape Town, South Africa.

Fortunate Shabalala (F)

University of Eswatini, M48V+JXG, Mbabane, Eswatini.

Bongumusa R Simelane (BR)

Eswatini Business Health and Wellness, Malagwane Hill, Mbabane, Eswatini.

Lisa Stehr (L)

Heidelberg Institute of Global Health, Heidelberg University, Im Neuenheimer Feld 130.3, 69120, Heidelberg, Germany.

Fabrizio Tediosi (F)

Swiss Tropical and Public Health Institute, Kreuzstrasse 2, 4123, Allschwil, Switzerland.
University of Basel, Basel, Switzerland.

Frank van Leth (F)

Amsterdam Public Health Research Institute, Amsterdam, Netherlands.
Department of Health Sciences, Vrije Universiteit, De Boelelaan 1105, 1081 HV, Amsterdam, The Netherlands.

Jan-Walter De Neve (JW)

Heidelberg Institute of Global Health, Heidelberg University, Im Neuenheimer Feld 130.3, 69120, Heidelberg, Germany.

Till Bärnighausen (T)

Heidelberg Institute of Global Health, Heidelberg University, Im Neuenheimer Feld 130.3, 69120, Heidelberg, Germany.
Harvard Center for Population and Development Studies, Cambridge, USA.
Africa Health Research Institute, KwaZulu-Natal, 3935, South Africa.

Pascal Geldsetzer (P)

Division of Primary Care and Population Health, Stanford University, 291 Campus Drive, Stanford, CA, 94305-5101, USA. pgeldsetzer@gmail.com.
Chan Zuckerberg Biohub, San Francisco, CA, 94158, USA. pgeldsetzer@gmail.com.

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