Effectiveness of Integrated Care on Delaying Chronic Kidney Disease Progression in Rural Communities of Thailand (ESCORT)
Primary Purpose
Chronic Kidney Disease
Status
Completed
Phase
Not Applicable
Locations
Thailand
Study Type
Interventional
Intervention
Integrated Chronic Kidney Disease care
Conventional CKD care
Sponsored by
About this trial
This is an interventional treatment trial for Chronic Kidney Disease focused on measuring Chronic Kidney Disease, Integrated Chronic Kidney Disease Care, Village Health Volunteers
Eligibility Criteria
Inclusion Criteria:
- ages 18-70 years and known to have diabetes and/or hypertension.
- eGFR are in a range of 15 - 59 ml/min/1.73m2 estimated twice at 3 months.
Exclusion Criteria:
- unstable/advanced cardiovascular disease
- active glomerular disease, obstructive uropathy, end-stage renal disease, HIV infection, pregnancy, body mass index (BMI) less than 18 or more than 40 kg/m2, being under treatment for malignancy, urine protein-creatinine ratio more than 3.5 g/g creatinine and active urinary sediment (urine red blood cells >3 cells/high power field or urine white blood cells >10 cells/high power field).
Sites / Locations
- Bhumirajanagarindra Kidney Institute
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Integrated Chronic Kidney Disease care
Conventional CKD care
Arm Description
standard guidelines of CKD treatment + Integrated CKD care consisting of multidisciplinary team care and home visit by community care network
standard guidelines of CKD treatment
Outcomes
Primary Outcome Measures
The difference of rate of estimated glomerular filtration rate (eGFR) decline
We compare the difference of rate of estimated glomerular filtration rate (eGFR) decline between intervention group and control group from baseline to the end of the study.
Secondary Outcome Measures
Cardiovascular Morbidity or Event
The definitions of cardiovascular event in this study are the numbers of myocardial infarction, stroke including ischemic and hemorrhagic event.
Incidence of Initiation of Renal Replacement Therapy
Incidence of initiation of renal replacement therapy consisting of hemodialysis, peritoneal dialysis, and kidney transplantation.
Hospitalization
The definitions of hospitalization in the study are any medical problem that relevant to cardiovascular disease and kidney problem which physician decide to admit the patients.
Change from baseline in Systolic Blood Pressure at 24 months
Blood pressure will be recorded twice with a sphygmomanometer with a 15-minute rest interval during each hospital visit of both groups
Change from baseline in amount of proteinuria at 24 months
Changes in amount of proteinuria which is measured by using urine protein-creatinine ratio.
Change from Baseline in Hemoglobin A1C at 24 months
We compare the difference of hemoglobin A1C of diabetic patients between intervention and control group.
Change from baseline in 24 hour urine sodium at 24 months
To evaluate amount of sodium intake, we compare the difference of 24 hour urine sodium between intervention group and control group.
Change from baseline in Protein Intake at 24 months
We compare the amount of protein intake by using normalized Protein Nitrogen Appearance, which will be calculated from 24 hour urine urea and ideal body weight.
Full Information
NCT ID
NCT01978951
First Posted
December 8, 2012
Last Updated
March 29, 2014
Sponsor
Bhumirajanagarindra Kidney Institute, Thailand
Collaborators
Ministry of Health, Thailand
1. Study Identification
Unique Protocol Identification Number
NCT01978951
Brief Title
Effectiveness of Integrated Care on Delaying Chronic Kidney Disease Progression in Rural Communities of Thailand
Acronym
ESCORT
Official Title
Effectiveness of Integrated Care on Delaying Chronic Kidney Disease Progression in Rural Communities of Thailand (ESCORT Study)
Study Type
Interventional
2. Study Status
Record Verification Date
March 2014
Overall Recruitment Status
Completed
Study Start Date
July 2011 (undefined)
Primary Completion Date
July 2013 (Actual)
Study Completion Date
December 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Bhumirajanagarindra Kidney Institute, Thailand
Collaborators
Ministry of Health, Thailand
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
If primary health-care officers and Villages Health Volunteers (VHVs) be trained to render proper CKD care, it is interesting if their intimate relationship and commitment to their responsible village households will result in better outcomes when compared with the conventional care model as mention above. In this project, we plan to compare the effectiveness of a conventional care program against an integrated multidisciplinary CKD care program provided by nephrologists in conjunction with well-trained paramedical personnel and VHVs on CKD progression.
Detailed Description
Background The unique characteristic of community-health care in Thailand is a system of primary- health care officers and Village Health Volunteers (VHVs) providing basic health care to more than 90% of Thai population. Should these allied personnel be trained on how to render proper chronic kidney disease (CKD) care, it would be interesting to study whether their role play care will result in better quality of CKD care.
Design This study is a community-based cluster randomized controlled trial to be conducted in 2 districts of Kamphaeng Phet Province, located about 400 kilometers north of Bangkok. About 300 stage 3-4 CKD patients will be enrolled to each of the 2 treatment groups. Patients in both groups will be treated according to The National Kidney Foundation Kidney Disease Outcomes Quality Initiative guidelines. The District 1 (control group) patients will be provided a conventional CKD care. For the District 2 (intervention group) patients, an integrated CKD care program will be provided by the multidisciplinary team of district hospital in conjunction with the community CKD care networks (i.e. primary-health care officers and VHVs). The key activities of integrated CKD care program are live demonstration about treatment and optimal diets for CKD patients which will be provided during each hospital visit and quarterly home visits. Clinical and laboratory parameters of all cases will be assessed every 3 months. Duration of the study is 24 months. The primary outcome of this study is the rate of eGFR decline. The secondary outcomes are time of initiation of dialysis, cardiovascular mortality, and all-cause mortality.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Kidney Disease
Keywords
Chronic Kidney Disease, Integrated Chronic Kidney Disease Care, Village Health Volunteers
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
443 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Integrated Chronic Kidney Disease care
Arm Type
Experimental
Arm Description
standard guidelines of CKD treatment + Integrated CKD care consisting of multidisciplinary team care and home visit by community care network
Arm Title
Conventional CKD care
Arm Type
Active Comparator
Arm Description
standard guidelines of CKD treatment
Intervention Type
Behavioral
Intervention Name(s)
Integrated Chronic Kidney Disease care
Other Intervention Name(s)
Multidisciplinary team + Community CKD care network
Intervention Description
Activities of integrated CKD care program, which will be provided during each hospital visit and quarterly home visits, are live demonstration about treatment and optimal diets for CKD patients, monitor drug compliance.
Intervention Type
Behavioral
Intervention Name(s)
Conventional CKD care
Other Intervention Name(s)
group counselling
Intervention Description
group counselling about optimal diets for CKD patients
Primary Outcome Measure Information:
Title
The difference of rate of estimated glomerular filtration rate (eGFR) decline
Description
We compare the difference of rate of estimated glomerular filtration rate (eGFR) decline between intervention group and control group from baseline to the end of the study.
Time Frame
30 months
Secondary Outcome Measure Information:
Title
Cardiovascular Morbidity or Event
Description
The definitions of cardiovascular event in this study are the numbers of myocardial infarction, stroke including ischemic and hemorrhagic event.
Time Frame
24 months
Title
Incidence of Initiation of Renal Replacement Therapy
Description
Incidence of initiation of renal replacement therapy consisting of hemodialysis, peritoneal dialysis, and kidney transplantation.
Time Frame
24 months
Title
Hospitalization
Description
The definitions of hospitalization in the study are any medical problem that relevant to cardiovascular disease and kidney problem which physician decide to admit the patients.
Time Frame
24 months
Title
Change from baseline in Systolic Blood Pressure at 24 months
Description
Blood pressure will be recorded twice with a sphygmomanometer with a 15-minute rest interval during each hospital visit of both groups
Time Frame
24 months
Title
Change from baseline in amount of proteinuria at 24 months
Description
Changes in amount of proteinuria which is measured by using urine protein-creatinine ratio.
Time Frame
24 months
Title
Change from Baseline in Hemoglobin A1C at 24 months
Description
We compare the difference of hemoglobin A1C of diabetic patients between intervention and control group.
Time Frame
24 months
Title
Change from baseline in 24 hour urine sodium at 24 months
Description
To evaluate amount of sodium intake, we compare the difference of 24 hour urine sodium between intervention group and control group.
Time Frame
24 months
Title
Change from baseline in Protein Intake at 24 months
Description
We compare the amount of protein intake by using normalized Protein Nitrogen Appearance, which will be calculated from 24 hour urine urea and ideal body weight.
Time Frame
24 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
ages 18-70 years and known to have diabetes and/or hypertension.
eGFR are in a range of 15 - 59 ml/min/1.73m2 estimated twice at 3 months.
Exclusion Criteria:
unstable/advanced cardiovascular disease
active glomerular disease, obstructive uropathy, end-stage renal disease, HIV infection, pregnancy, body mass index (BMI) less than 18 or more than 40 kg/m2, being under treatment for malignancy, urine protein-creatinine ratio more than 3.5 g/g creatinine and active urinary sediment (urine red blood cells >3 cells/high power field or urine white blood cells >10 cells/high power field).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Teerayuth Jiamjariyaporn, M.D.
Organizational Affiliation
Bhumirajanagarindra Kidney Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Bhumirajanagarindra Kidney Institute
City
Bangkok
ZIP/Postal Code
10400
Country
Thailand
12. IPD Sharing Statement
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Effectiveness of Integrated Care on Delaying Chronic Kidney Disease Progression in Rural Communities of Thailand
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