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Community-based, eHealth Supported Type 2 Diabetes Care by Lay Village Health Workers in Rural Lesotho (ComBaCaL T2D)

Primary Purpose

Type 2 Diabetes Mellitus (T2D)

Status
Recruiting
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
T2D care package
Referral to the responsible health facility
Sponsored by
University Hospital, Basel, Switzerland
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Type 2 Diabetes Mellitus (T2D) focused on measuring Community-Based Chronic Disease Care Lesotho (ComBaCaL) cohort study, low- and middle-income countries (LMICs), lay healthcare worker (LHW), chronic care village health worker (CC-VHW), chronic care nurse (CC nurse), non-communicable disease (NCD), blood glucose (BG), cardiovascular disease risk factor (CVDRF), glycated haemoglobin (HbA1c), Lesotho Ministry of Health (MoH) Village Health Worker Program, first-line antidiabetics, first-line lipid-lowering treatment

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Participant of the ComBaCaL cohort study (signed informed consent available) Living with T2D, defined as reporting intake of antidiabetic medication or being newly diagnosed during screening via standard diagnostic algorithm Exclusion Criteria: Known type 1 diabetes mellitus Reported pregnancy

Sites / Locations

  • SolidarMed LesothoRecruiting
  • University of Basel, Division of Clinical EpidemiologyRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Intervention villages

Control villages

Arm Description

In the intervention villages, CC-VHWs will offer a T2D care package including lifestyle counselling, firstline antidiabetic (metformin) and lipid-lowering (statin) treatment for uncomplicated T2D and treatment support and regular check-ups for complicated T2D at village-level according to clinical algorithms based on international guidelines for primary healthcare management of T2D and the updated Lesotho Standard Treatment Guidelines. Direct guidance for treatment initiation, drug prescription, counselling and monitoring will be provided via the ComBaCaL app. In case of complicated disease (i.e. if treatment targets are not reached with metformin alone), unclear diagnosis, relevant comorbidities or presence of clinical alarm signs or symptoms, participants will be referred to the closest health facility for further management.

In control villages, CC-VHWs will refer participants to the responsible health facility for therapeutic management after enrolment and baseline assessment.

Outcomes

Primary Outcome Measures

Mean HbA1c (in percent)
Mean HbA1c (in percent)

Secondary Outcome Measures

Change in 10-year CVD risk estimated
Change in 10-year CVD risk estimated using the World Health Organization (WHO) CVD risk prediction tool
Mean HbA1c (in percent)
Mean HbA1c (in percent)
Change in mean fasting blood glucose (FBG) (mmol/l)
Change in mean fasting blood glucose (FBG) (mmol/l)
Change in proportion of participants with an HbA1c below 8%
Change in proportion of participants with an HbA1c below 8%
Change in proportion of participants with an FBG below 7 mmol/l
Change in proportion of participants with an FBG below 7 mmol/l
Change in number of CVD risk factors
Change in number of CVD risk factors (such as smoking status, BMI, abdominal circumference, blood lipid status, blood pressure, dietary habits and physical activity)
Linkage to care: Change in proportion of participants not taking treatment at enrolment who have initiated pharmacological antidiabetic treatment
Change in proportion of participants not taking treatment at enrolment who have initiated pharmacological antidiabetic treatment
Engagement in care: Change in proportion of participants who are engaged in care
Change in proportion of participants who are engaged in care, defined as reporting intake of antidiabetic medication as per prescription of a healthcare provider or reaching treatment targets without intake of medication
Change in self-reported adherence to antidiabetic medication
Change in self-reported adherence to antidiabetic medication
Occurrence of Serious Adverse Events (SAEs) and Adverse Events of Special Interest (AESIs)
Occurrence of Serious Adverse Events (SAEs) and Adverse Events of Special Interest (AESIs)

Full Information

First Posted
February 14, 2023
Last Updated
October 10, 2023
Sponsor
University Hospital, Basel, Switzerland
Collaborators
Swiss Agency for Development and Cooperation (SDC), World Diabetes Foundation (WDF), SolidarMed
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1. Study Identification

Unique Protocol Identification Number
NCT05743387
Brief Title
Community-based, eHealth Supported Type 2 Diabetes Care by Lay Village Health Workers in Rural Lesotho
Acronym
ComBaCaL T2D
Official Title
Community-based, eHealth Supported Type 2 Diabetes Care by Lay Village Health Workers in Rural Lesotho Protocol for a Cluster-randomized Trial Within the ComBaCaL Cohort Study (ComBaCaL T2D TwiC)
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 13, 2023 (Actual)
Primary Completion Date
August 2024 (Anticipated)
Study Completion Date
August 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Basel, Switzerland
Collaborators
Swiss Agency for Development and Cooperation (SDC), World Diabetes Foundation (WDF), SolidarMed

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This cluster-randomized intervention is embedded in the ComBaCaL (Community-Based Chronic disease care Lesotho) cohort study (EKNZ ID AO_2022-00058, clinicaltrials.gov ID NCT05596773, Lesotho NH-REC ID 210-2022), a platform for the investigation of chronic diseases and their management in rural Lesotho that is maintained by local lay chronic care village health workers (CC-VHWs). The overall objective of the ComBaCaL cohort study and nested TwiCs is to assess the impact of eHealthsupported, lay-led chronic disease control measures in rural Lesotho. In this T2D TwiC, the effect, safety and feasibility of a community-based T2D care package (which includes the offer of first-line oral antidiabetic and lipid-lowering treatment for uncomplicated T2D by lay CC-VHWs in comparison to facility-based care after community-based screening and diagnosis) will be evaluated.
Detailed Description
Globally, 9.3% of the adult population or 436 million individuals were estimated to be living with diabetes in 2019. Until 2045 this number is expected to increase by more than 50% to over 700 million. Four out of five people affected by diabetes are currently living in low- and middle-income countries (LMICs). Over 90% of all diabetes cases are due to type 2 diabetes (T2D) which is also the main driver of the projected increase in overall diabetes cases. The increase in T2D prevalence is caused by ageing populations and changing lifestyles with decreasing levels of physical activity and higher caloric diets and associated obesity. This cluster-randomized intervention is embedded in the ComBaCaL (Community-Based Chronic disease care Lesotho) cohort study (EKNZ ID AO_2022-00058, clinicaltrials.gov ID NCT05596773, Lesotho NH-REC ID 210-2022), a platform for the investigation of chronic diseases and their management in rural Lesotho that is maintained by local lay chronic care village health workers (CC-VHWs). In this trial, using the Trials within Cohorts (TwiCs) approach, it will be analyzed whether an LHW-led model could be capacitated to safely and effectively provide first-line management (including oral antidiabetic, lipid-lowering treatment and lifestyle counselling) at community-level. In villages randomized to the intervention arm, lay Chronic Care Village Health Workers (CCVHWs) operating within the existing Ministry of Health (MoH) village health worker system will be capacitated to screen for and diagnose T2D, to provide lifestyle counselling, to prescribe and to monitor first-line antidiabetic and lipid-lowering treatment for uncomplicated T2D and to provide treatment support for complicated T2D, supported by a tailored clinical decision support application (ComBaCaL app) in their villages. The control group consists of people diagnosed with T2D living in villages that are also part of the ComBaCaL cohort but not sampled for the intervention (control villages), where CC-VHWs will only screen for and diagnose T2D with subsequent standardized counselling and referral to the closest health facility if T2D is present, but no village-based prescriptions. The overall objective of the ComBaCaL cohort study and nested TwiCs is to assess the impact of eHealthsupported, lay-led chronic disease control measures in rural Lesotho.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes Mellitus (T2D)
Keywords
Community-Based Chronic Disease Care Lesotho (ComBaCaL) cohort study, low- and middle-income countries (LMICs), lay healthcare worker (LHW), chronic care village health worker (CC-VHW), chronic care nurse (CC nurse), non-communicable disease (NCD), blood glucose (BG), cardiovascular disease risk factor (CVDRF), glycated haemoglobin (HbA1c), Lesotho Ministry of Health (MoH) Village Health Worker Program, first-line antidiabetics, first-line lipid-lowering treatment

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Cluster-randomized controlled trial nested within the ComBaCaL cohort study following a trial within cohort (TwiC) approach. 50% of the villages being part of the overarching ComBaCaL cohort will be randomized stratified by district and access to health facility to receive the intervention.
Masking
Outcomes Assessor
Masking Description
Participants are not blinded to the intervention due to the nature of the intervention. Due to the cluster level randomization and TwiCs approach participants are blinded to the allocation (i.e. participants in the control villages are not aware of the intervention being implemented in the intervention villages). The main outcome and the safety endpoints are assessed by an independent study physician blinded to the allocation. The statistician and data managers cannot be blinded to the allocation.
Allocation
Randomized
Enrollment
240 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention villages
Arm Type
Active Comparator
Arm Description
In the intervention villages, CC-VHWs will offer a T2D care package including lifestyle counselling, firstline antidiabetic (metformin) and lipid-lowering (statin) treatment for uncomplicated T2D and treatment support and regular check-ups for complicated T2D at village-level according to clinical algorithms based on international guidelines for primary healthcare management of T2D and the updated Lesotho Standard Treatment Guidelines. Direct guidance for treatment initiation, drug prescription, counselling and monitoring will be provided via the ComBaCaL app. In case of complicated disease (i.e. if treatment targets are not reached with metformin alone), unclear diagnosis, relevant comorbidities or presence of clinical alarm signs or symptoms, participants will be referred to the closest health facility for further management.
Arm Title
Control villages
Arm Type
Active Comparator
Arm Description
In control villages, CC-VHWs will refer participants to the responsible health facility for therapeutic management after enrolment and baseline assessment.
Intervention Type
Other
Intervention Name(s)
T2D care package
Intervention Description
T2D care package including lifestyle counselling, firstline antidiabetic (metformin) and lipid-lowering (statin) treatment for uncomplicated T2D and treatment support and regular check-ups for complicated T2D at village-level. Guidance will be provided via the ComBaCaL app. In case of complicated disease referral to the closest health facility for further management.
Intervention Type
Other
Intervention Name(s)
Referral to the responsible health facility
Intervention Description
CC-VHWs will refer participants to the responsible health facility for therapeutic management. The ComBaCaL app supports clinical decision making and documentation for screening, diagnosis and referral, but not prescription/provision and monitoring of antidiabetic or lipid-lowering medication for uncomplicated T2D patients or treatment support for complicated T2D patients.
Primary Outcome Measure Information:
Title
Mean HbA1c (in percent)
Description
Mean HbA1c (in percent)
Time Frame
12 months after enrolment
Secondary Outcome Measure Information:
Title
Change in 10-year CVD risk estimated
Description
Change in 10-year CVD risk estimated using the World Health Organization (WHO) CVD risk prediction tool
Time Frame
6 and 12 months after enrolment
Title
Mean HbA1c (in percent)
Description
Mean HbA1c (in percent)
Time Frame
6 months after enrolment
Title
Change in mean fasting blood glucose (FBG) (mmol/l)
Description
Change in mean fasting blood glucose (FBG) (mmol/l)
Time Frame
6 and 12 months after enrolment
Title
Change in proportion of participants with an HbA1c below 8%
Description
Change in proportion of participants with an HbA1c below 8%
Time Frame
6 and 12 months after enrolment
Title
Change in proportion of participants with an FBG below 7 mmol/l
Description
Change in proportion of participants with an FBG below 7 mmol/l
Time Frame
6 and 12 months after enrolment
Title
Change in number of CVD risk factors
Description
Change in number of CVD risk factors (such as smoking status, BMI, abdominal circumference, blood lipid status, blood pressure, dietary habits and physical activity)
Time Frame
6 and 12 months after enrolment
Title
Linkage to care: Change in proportion of participants not taking treatment at enrolment who have initiated pharmacological antidiabetic treatment
Description
Change in proportion of participants not taking treatment at enrolment who have initiated pharmacological antidiabetic treatment
Time Frame
6 and 12 months after enrolment
Title
Engagement in care: Change in proportion of participants who are engaged in care
Description
Change in proportion of participants who are engaged in care, defined as reporting intake of antidiabetic medication as per prescription of a healthcare provider or reaching treatment targets without intake of medication
Time Frame
6 and 12 months after enrolment
Title
Change in self-reported adherence to antidiabetic medication
Description
Change in self-reported adherence to antidiabetic medication
Time Frame
6 and 12 months after enrolment
Title
Occurrence of Serious Adverse Events (SAEs) and Adverse Events of Special Interest (AESIs)
Description
Occurrence of Serious Adverse Events (SAEs) and Adverse Events of Special Interest (AESIs)
Time Frame
within 6 and 12 months after enrolment
Other Pre-specified Outcome Measures:
Title
Number of consultations (at a health facility and with the CC-VHW)
Description
Number of consultations at a health facility and with the CC-VHW
Time Frame
within 6 and 12 months after enrolment
Title
Trajectory of participants between facility-based and community-based care in the intervention villages
Description
Trajectory of participants between facility-based and community-based care in the intervention villages (i.e. number of participants accepting community-based care at baseline, number of people switching to facility-based care and back to community-based care
Time Frame
during the study period (up to 12 months)
Title
Proportion of participants with T2D who stop drug treatment or interrupt drug treatment for more than three weeks or require a switch of drug treatment due to (perceived) adverse events (AEs)
Description
Proportion of participants with T2D who stop drug treatment or interrupt drug treatment for more than three weeks or require a switch of drug treatment due to (perceived) adverse events (AEs)
Time Frame
within 6 and 12 months after enrolment
Title
Change in proportion of participants who are reaching treatment targets (FBG <7 mmol/l) and are reporting no intake of antidiabetic medication in the two weeks prior to assessment
Description
Change in proportion of participants who are reaching treatment targets (FBG <7 mmol/l) and are reporting no intake of antidiabetic medication in the two weeks prior to assessment
Time Frame
6 and 12 months after enrolment
Title
Change in proportion of participants accessing lipid-lowering medication
Description
Change in proportion of participants accessing lipid-lowering medication
Time Frame
6 and 12 months after enrolment
Title
Change in health system costs for the management of participants condition
Description
Change in health system costs for the management of participants condition
Time Frame
within 6 and 12 months after diagnosis
Title
Change in individual costs for participants for the management of their condition
Description
Change in individual costs for participants for the management of their condition
Time Frame
within 6 and 12 months after diagnosis
Title
Change in10-year CVD risk estimated using the Globorisk score
Description
Change in10-year CVD risk estimated using the Globorisk score, a cardiovascular disease risk score that predicts risk of heart attack or stroke in healthy individuals for all countries in the world. It uses information on a person's country of residence, age, sex, smoking, diabetes, blood pressure and cholesterol to predict the chance that they would have a heart attack or stroke in the next 10 years.
Time Frame
6 and 12 months after enrolment
Title
Change in10-year CVD risk estimated using the Framingham Risk Score
Description
Change in10-year CVD risk estimated using the Framingham Risk Score, a sex-specific algorithm used to estimate the 10-year cardiovascular risk of an individual. The Framingham Risk Score was first developed based on data obtained from the Framingham Heart Study.
Time Frame
6 and 12 months after enrolment
Title
Quality of life (QOL) using the EQ-5D-5L instrument
Description
The EQ-5D-5L is a self-assessed, health related, quality of life questionnaire. The scale measures quality of life on a 5-component scale including mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. The QOL scores are summed so that a higher score indicates higher quality of life.
Time Frame
12 months after enrolment
Title
Health beliefs using the Beliefs about Medicines Questionnaire (BMQ) adapted for people living with T2D
Description
The BMQl comprises two 4-item factors assessing beliefs that medicines are harmful, addictive, poisons which should not be taken continuously and that medicines are overused by doctors.The items are scored on a 5 point Likert scale with scores ranging from 4 to 20.
Time Frame
12 months after enrolment
Title
Diabetes distress using the five item version of the "Problem Areas in Diabetes" (PAID-5) scale Problem Areas in Diabetes Scale-Five-item Short Form
Description
Problem Areas in Diabetes Scale-Five-item Short Form. Total scores on the PAID-5 can range from 0 to 20, with higher scores suggesting greater diabetes-related emotional distress.
Time Frame
12 months after enrolment
Title
Change in dosage of antidiabetic medications prescribed by CC-VHWs or healthcare professionals
Description
Change in dosage of antidiabetic medications prescribed by CC-VHWs or healthcare professionals
Time Frame
6 and 12 months after enrolment
Title
Change in dosage of lipid-lowering medications prescribed by CC-VHWs or healthcare professionals
Description
Change in dosage of lipid-lowering medications prescribed by CC-VHWs or healthcare professionals
Time Frame
6 and 12 months after enrolment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Participant of the ComBaCaL cohort study (signed informed consent available) Living with T2D, defined as reporting intake of antidiabetic medication or being newly diagnosed during screening via standard diagnostic algorithm Exclusion Criteria: Known type 1 diabetes mellitus Reported pregnancy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Niklaus Labhardt, Prof.
Phone
+41 79 870 18 59
Email
niklaus.labhardt@usb.ch
First Name & Middle Initial & Last Name or Official Title & Degree
Alain Amstutz, Dr.
Phone
+41 79 489 94 48
Email
alain.amstutz@usb.ch
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Niklaus Labhardt, Prof.
Organizational Affiliation
Division of Clinical Epidemiology, University Hospital Basel
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Alain Amstutz, MD
Organizational Affiliation
Division of Clinical Epidemiology, University Hospital Basel, University of Basel
Official's Role
Principal Investigator
Facility Information:
Facility Name
SolidarMed Lesotho
City
Maseru
Country
Lesotho
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Irene Ayakaka, MD
Phone
+266 28325172
Email
ayakaka@gmail.com
First Name & Middle Initial & Last Name & Degree
Irene Ayakaka, MD
First Name & Middle Initial & Last Name & Degree
Ravi Gupta, MBBS
First Name & Middle Initial & Last Name & Degree
Mamakhala Chitja, MBBS
Facility Name
University of Basel, Division of Clinical Epidemiology
City
Basel
ZIP/Postal Code
4051
Country
Switzerland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Niklaus Labhardt, Prof.
Phone
+41 79 870 18 59
Email
niklaus.labhardt@usb.ch
First Name & Middle Initial & Last Name & Degree
Felix Gerber
Phone
+41 78 704 08 85
Email
felix.gerber@usb.ch
First Name & Middle Initial & Last Name & Degree
Niklaus Labhardt, Prof.
First Name & Middle Initial & Last Name & Degree
Alain Amstutz, MD
First Name & Middle Initial & Last Name & Degree
Thabo Lejone
First Name & Middle Initial & Last Name & Degree
Felix Gerber

12. IPD Sharing Statement

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Community-based, eHealth Supported Type 2 Diabetes Care by Lay Village Health Workers in Rural Lesotho

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