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Using a Diabetic Kidney Disease (DKD) Registry to Treat to Multiple Targets (TMT) (DKD-TMT)

Primary Purpose

Diabetic Kidney Disease

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Telephone Reminder
Doctor-Nurse Follow Up
Personalized Risk Report for Patient Empowerment
Sponsored by
Asia Diabetes Foundation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetic Kidney Disease focused on measuring Diabetic Kidney Disease, Diabetes, Asian, Joint Asia Diabetes Evaluation (JADE) Program

Eligibility Criteria

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

Inclusion Criteria:

  • Type 2 diabetic patients with serum creatinine above 30% upper limit of normal of the laboratory range and/or estimated glomerular filtration rate (eGFR)< 65ml/min/1.73m2; or type 2 diabetic patients with both eGFR between 60 to 90ml/min/1.73m2 and urine albumin creatinine ratio (ACR) ≥ 25 mg/mmol.
  • Willingness to return for regular follow up visits

Exclusion Criteria:

  • Inability to give informed consent
  • Life threatening condition with reduced life expectancy
  • Patients on dialysis or eGFR<15 ml/min/1.732

Sites / Locations

  • The Forth Affiliated Hospital of China Medical University
  • Chinese University of Hong Kong, Prince of Wales Hospital
  • Department of Medicine, Alice Ho Miu Ling Nethersole Hospital
  • Bucheon St. Mary's Hospital, The Catholic University of Korea
  • Hally University Dongtan Sacred Heart Hospital
  • Seoul St.Mary's Hospital, The Catholic Unviersity of Korea
  • Universiti Sains Malysia
  • University Malaya Medical Centre, University of Malaya
  • Taipei Veterans General Hospital
  • Theptarin Hospital
  • Hoa Hao MEDIC Company LMT

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

No Intervention

Experimental

Experimental

Arm Label

Usual Care Group

Empowered Care Group

Team-based, Empowered Care Group

Arm Description

Usual care (UC) group: After undergoing a comprehensive assessment, all patients will receive UC in accordance to the practice of the health institution and return at 12 months for a repeat comprehensive assessment.

Empowered care (EC) group: After undergoing a comprehensive assessment, all patients will be given a JADE comprehensive assessment report which is a personalize risk report with treatment targets and decision support with explanation from the doctor and nurse. In addition to receiving UC in accordance to the practice of the health institution, the nurse will provide telephone reminder to patient 3-monthly to remind them to adhere to treatment, provide support and empower them to discuss with their doctors about their treatment needs and any concerns. All patients will return at 12 month for a repeat comprehensive assessment.

Team-based, empowered care (TEC) group: After undergoing a comprehensive assessment, patients randomized to the TEC group will be given a JADE comprehensive assessment report which is a personalized risk report for patient empowerment. They will receive telephone reminders and doctor-nurse follow up at least 3 monthly to achieve multiple targets recommended. The patients will also be given JADE reports 3-monthly and return at 12 month for a repeat comprehensive assessment.

Outcomes

Primary Outcome Measures

Attainment of at least 3 treatment targets
Attainment of at least 3 treatment targets of A1c<7% BP<130/80 mmHg LDL-C<1.8 mmol/L Triglyceride<1.7 mmol/L Persistence with RAS inhibitors taking into consideration safety and tolerability (e.g. hypoglycemia, hypotension, changes in electrolytes)

Secondary Outcome Measures

Incidence of all-diabetes related endpoints
Incidence of all-diabetes related endpoints (vascular, cancer, non-vascular non-cancer and all-cause death) between patients who attain at least 3 targets versus those who do not

Full Information

First Posted
April 28, 2014
Last Updated
April 12, 2022
Sponsor
Asia Diabetes Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT02176278
Brief Title
Using a Diabetic Kidney Disease (DKD) Registry to Treat to Multiple Targets (TMT)
Acronym
DKD-TMT
Official Title
Using a Diabetic Kidney Disease (DKD) Registry to Treat to Multiple Targets (TMT) (DKD-TMT)
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Completed
Study Start Date
June 2014 (Actual)
Primary Completion Date
February 2019 (Actual)
Study Completion Date
February 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Asia Diabetes Foundation

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
In this quality improvement program (DKD-TMT), patients will be recruited from multiple sites across Asia, with each site recruiting at least 300 type 2 diabetic patients with Diabetic Kidney Disease (DKD). After explanation by trained doctors and nurses, and with written informed consent, patients will be randomized to the UC (n=100, usual care) group, the EC (n=100, empowered care) group, or the TEC (n=100, team-based, empowered care) group. Patients in all 3 groups will undergo a comprehensive assessment (CA) guided by the templates in the Joint Asia Diabetes Evaluation (JADE) portal at baseline and at month 12. They will also self-administer a set of questionnaires for assessing quality of life and psychological distress during the CA at both time points. During the 12 months between the 2 CAs: Patients in the UC group will receive UC in accordance to the practice of the health institution. Patients in the EC group will receive a JADE summary report with personalized risk prediction, treatment targets and decision support with explanation from the doctor and nurse. In addition to receiving UC in accordance to the practice of the health institution, the nurse will telephone the patient 3-monthly to remind them to adhere to treatment, provide support and empower them to discuss with their doctors about their treatment needs and any concerns. Patients in the TEC group will be followed by a doctor-nurse team at least 3 monthly to achieve multiple targets, but tailored to patients' risk profile. The patients will receive telephone reminders and also be given a JADE follow up report 3-monthly. The primary composite endpoint is attainment of treatment goals and/or control of risk factors. The secondary composite endpoint is all-diabetes related clinical endpoints. The tertiary changes are behavioral changes, psychological well-being and quality of life.
Detailed Description
Hypothesis: Patient empowerment and team-based care augmented by the JADE program with features of risk stratification and decision support improves multiple risk factor control in Asian type 2 diabetic patients with chronic kidney disease. Attaining multiple treatment targets reduces all diabetes-related endpoints in these high risk patients. Objectives: To use the JADE program which 1) includes task delegation and change in workflow augmented by 2) a web-based portal consisting of features of risk stratification, feedback, recommendations and decision support to set up a DKD registry in order to 1) document control of risk factors and care standards in real practice in Asian type 2 diabetic patients; 2) empower doctors and patients to make informed decisions and 3) use a team approach to treat to multiple targets and reduce all diabetes related clinical outcomes. Study design: This will be a multicentre randomized translational program to compare the effects of usual care (UC) versus empowered care (EC) versus team-based, empowered care (TEC) on risk factor control and clinical outcomes in 3000 patients with DKD in Asian countries. Intervention: All patients will undergo a comprehensive assessment (CA) guided by the templates in the JADE portal at baseline and at month 12. All patients will also self-administer a set of questionnaires for assessing quality of life (EQ-5D-3L, WHOQOL-BREF, and a Time Trade-Off (TTO) question) and psychological distress (PHQ-9 and DASS-21) during the CA at baseline and at month 12. During the 12 months between the 2 CAs: Patients in the UC group will receive UC in accordance to the practice of the health institution. Patients in the EC group will receive a JADE summary report with personalized risk prediction, treatment targets and decision support with explanation from the doctor and nurse. In addition to receiving UC in accordance to the practice of the health institution, the nurse will telephone the patient 3-monthly to remind them to adhere to treatment, provide support and empower them to discuss with their doctors about their treatment needs and any concerns. Patients in the TEC group will be followed by a doctor-nurse team at least 3 monthly to achieve multiple targets, but tailored to patients' risk profile. The patients will receive telephone reminders and also be given a JADE follow up report 3-monthly. Outcome: The primary composite endpoint is attainment of treatment goals and/or control of risk factors. The secondary composite endpoint is all-diabetes related clinical endpoints. The tertiary changes are behavioral changes, psychological well-being and quality of life.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Kidney Disease
Keywords
Diabetic Kidney Disease, Diabetes, Asian, Joint Asia Diabetes Evaluation (JADE) Program

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
2400 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Usual Care Group
Arm Type
No Intervention
Arm Description
Usual care (UC) group: After undergoing a comprehensive assessment, all patients will receive UC in accordance to the practice of the health institution and return at 12 months for a repeat comprehensive assessment.
Arm Title
Empowered Care Group
Arm Type
Experimental
Arm Description
Empowered care (EC) group: After undergoing a comprehensive assessment, all patients will be given a JADE comprehensive assessment report which is a personalize risk report with treatment targets and decision support with explanation from the doctor and nurse. In addition to receiving UC in accordance to the practice of the health institution, the nurse will provide telephone reminder to patient 3-monthly to remind them to adhere to treatment, provide support and empower them to discuss with their doctors about their treatment needs and any concerns. All patients will return at 12 month for a repeat comprehensive assessment.
Arm Title
Team-based, Empowered Care Group
Arm Type
Experimental
Arm Description
Team-based, empowered care (TEC) group: After undergoing a comprehensive assessment, patients randomized to the TEC group will be given a JADE comprehensive assessment report which is a personalized risk report for patient empowerment. They will receive telephone reminders and doctor-nurse follow up at least 3 monthly to achieve multiple targets recommended. The patients will also be given JADE reports 3-monthly and return at 12 month for a repeat comprehensive assessment.
Intervention Type
Other
Intervention Name(s)
Telephone Reminder
Intervention Description
Nurse will provide telephone contact to patients every 3 month to remind them to adhere to treatment, provide support and empower them to discuss with their doctors about their treatment needs and any concerns
Intervention Type
Other
Intervention Name(s)
Doctor-Nurse Follow Up
Intervention Description
Patient will be followed by a doctor-nurse team at least 3 monthly to achieve multiple targets recommended as A1c<7%, BP<130/80 mmHg, LDL-C<1.8 mmol/l, triglyceride<1.7 mmol/l and persistence with RAS inhibitors taking into consideration safety and tolerability (e.g. hypoglycemia, hypotension, changes in electrolytes). Patient report will be given after follow up.
Intervention Type
Other
Intervention Name(s)
Personalized Risk Report for Patient Empowerment
Intervention Description
Patients will be given with personalized risk reports after baseline and 12-month repeat comprehensive assessments.
Primary Outcome Measure Information:
Title
Attainment of at least 3 treatment targets
Description
Attainment of at least 3 treatment targets of A1c<7% BP<130/80 mmHg LDL-C<1.8 mmol/L Triglyceride<1.7 mmol/L Persistence with RAS inhibitors taking into consideration safety and tolerability (e.g. hypoglycemia, hypotension, changes in electrolytes)
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Incidence of all-diabetes related endpoints
Description
Incidence of all-diabetes related endpoints (vascular, cancer, non-vascular non-cancer and all-cause death) between patients who attain at least 3 targets versus those who do not
Time Frame
1 year
Other Pre-specified Outcome Measures:
Title
Changes in A1c
Description
To examine the absolute and % changes in A1c amongst the UC, EC and TEC groups
Time Frame
1 Year
Title
Changes in eGFR
Description
To examine the absolute and % changes in eGFR amongst the UC, EC and TEC groups
Time Frame
1 Year
Title
Use of medication
Description
To understand the use of medications including statins, RAS inhibitors and insulin amongst the UC, EC and TEC groups
Time Frame
1 year
Title
Incidence of ESRD and all-cause death
Description
To examine the difference of incidence of ESRD and all-cause death between patients who are treated to multiple targets and those who are not
Time Frame
1 year
Title
Incidence of all CV events
Description
To investiage the difference of incidence of all CV events including stroke, acute myocardial infarction, heart failure, acute coronary syndrome, all-cause death between patients who are treated to multiple targets and those who are not
Time Frame
1 year
Title
Incidence of all-site cancer and all-cause death
Description
To examine incidence of all-site cancer and all-cause death between patients who are treated to multiple targets and those who are not
Time Frame
1 year
Title
Cost-effectiveness and quality of life analysis
Time Frame
1 year
Title
Changes in lipid
Description
To examine the absolute and % changes in lipids amongst the UC, EC and TEC groups
Time Frame
1 year
Title
Changes in BP
Description
To examine the absolute and % changes in BP amongst the UC, EC and TEC groups
Time Frame
1 year
Title
Changes in body weight
Description
To exmine the absolute and % changes in body weight amongst the UC, EC and TEC groups
Time Frame
1 year
Title
Changes in albuminuria
Description
To exmine the absolute and % changes albuminuria amongst the UC, EC and TEC groups
Time Frame
1 year

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Type 2 diabetic patients with serum creatinine above 30% upper limit of normal of the laboratory range and/or estimated glomerular filtration rate (eGFR)< 65ml/min/1.73m2; or type 2 diabetic patients with both eGFR between 60 to 90ml/min/1.73m2 and urine albumin creatinine ratio (ACR) ≥ 25 mg/mmol. Willingness to return for regular follow up visits Exclusion Criteria: Inability to give informed consent Life threatening condition with reduced life expectancy Patients on dialysis or eGFR<15 ml/min/1.732
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Juliana CN Chan, MD
Organizational Affiliation
Asia Diabetes Foundation
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Forth Affiliated Hospital of China Medical University
City
Shengyang
Country
China
Facility Name
Chinese University of Hong Kong, Prince of Wales Hospital
City
Hong Kong
Country
Hong Kong
Facility Name
Department of Medicine, Alice Ho Miu Ling Nethersole Hospital
City
Hong Kong
Country
Hong Kong
Facility Name
Bucheon St. Mary's Hospital, The Catholic University of Korea
City
Seoul
State/Province
Gyenonggo-do
Country
Korea, Republic of
Facility Name
Hally University Dongtan Sacred Heart Hospital
City
Gyeonggi-do
Country
Korea, Republic of
Facility Name
Seoul St.Mary's Hospital, The Catholic Unviersity of Korea
City
Seoul
ZIP/Postal Code
137-701
Country
Korea, Republic of
Facility Name
Universiti Sains Malysia
City
Kubang Kerian
State/Province
Kelantan
Country
Malaysia
Facility Name
University Malaya Medical Centre, University of Malaya
City
Kuala Lumpur
Country
Malaysia
Facility Name
Taipei Veterans General Hospital
City
Taipei
Country
Taiwan
Facility Name
Theptarin Hospital
City
Bangkok
ZIP/Postal Code
10110
Country
Thailand
Facility Name
Hoa Hao MEDIC Company LMT
City
Ho Chi Minh
Country
Vietnam

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
19573118
Citation
Chan J, So W, Ko G, Tong P, Yang X, Ma R, Kong A, Wong R, Le Coguiec F, Tamesis B, Wolthers T, Lyubomirsky G, Chow P. The Joint Asia Diabetes Evaluation (JADE) Program: a web-based program to translate evidence to clinical practice in Type 2 diabetes. Diabet Med. 2009 Jul;26(7):693-9. doi: 10.1111/j.1464-5491.2009.02751.x.
Results Reference
background
PubMed Identifier
19460913
Citation
Chan JC, So WY, Yeung CY, Ko GT, Lau IT, Tsang MW, Lau KP, Siu SC, Li JK, Yeung VT, Leung WY, Tong PC; SURE Study Group. Effects of structured versus usual care on renal endpoint in type 2 diabetes: the SURE study: a randomized multicenter translational study. Diabetes Care. 2009 Jun;32(6):977-82. doi: 10.2337/dc08-1908.
Results Reference
background
PubMed Identifier
16916809
Citation
Wu JY, Leung WY, Chang S, Lee B, Zee B, Tong PC, Chan JC. Effectiveness of telephone counselling by a pharmacist in reducing mortality in patients receiving polypharmacy: randomised controlled trial. BMJ. 2006 Sep 9;333(7567):522. doi: 10.1136/bmj.38905.447118.2F. Epub 2006 Aug 17.
Results Reference
background
PubMed Identifier
16378791
Citation
Leung WY, So WY, Tong PC, Chan NN, Chan JC. Effects of structured care by a pharmacist-diabetes specialist team in patients with type 2 diabetic nephropathy. Am J Med. 2005 Dec;118(12):1414. doi: 10.1016/j.amjmed.2005.07.050.
Results Reference
background
PubMed Identifier
15280527
Citation
Leung WY, So WY, Tong PC, Lo MK, Lee KF, Ko GT, Chan WB, Cockram CS, Brenner BM, Shahinfar S, Critchley JA, Chan JC. The renoprotective effects of structured care in a clinical trial setting in type 2 diabetic patients with nephropathy. Nephrol Dial Transplant. 2004 Oct;19(10):2519-25. doi: 10.1093/ndt/gfh408. Epub 2004 Jul 27.
Results Reference
background
PubMed Identifier
24781960
Citation
Chan JC, Sui Y, Oldenburg B, Zhang Y, Chung HH, Goggins W, Au S, Brown N, Ozaki R, Wong RY, Ko GT, Fisher E; JADE and PEARL Project Team. Effects of telephone-based peer support in patients with type 2 diabetes mellitus receiving integrated care: a randomized clinical trial. JAMA Intern Med. 2014 Jun;174(6):972-81. doi: 10.1001/jamainternmed.2014.655.
Results Reference
background
PubMed Identifier
35333363
Citation
Chan JCN, Thewjitcharoen Y, Nguyen TK, Tan A, Chia YC, Hwu CM, Jian D, Himathongkam T, Wong KL, Choi YM, Mirasol R, Mohamed M, Kong APS, Ma RCW, Chow EYK, Ozaki R, Lau V, Fu AWC, Hong EG, Yoon KH, Tsang CC, Lau ESH, Lim LL, Luk AOY. Effect of a Web-Based Management Guide on Risk Factors in Patients With Type 2 Diabetes and Diabetic Kidney Disease: A JADE Randomized Clinical Trial. JAMA Netw Open. 2022 Mar 1;5(3):e223862. doi: 10.1001/jamanetworkopen.2022.3862.
Results Reference
derived
Links:
URL
https://www.adf.org.hk
Description
Asia Diabetes Foundation
URL
https://jamanetwork.com/journals/jamanetworkopen/fullarticle/2790519
Description
JAMA Network Open: Effect of a Web-Based Management Guide on Risk Factors in Patients With Type 2 Diabetes and Diabetic Kidney Disease

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Using a Diabetic Kidney Disease (DKD) Registry to Treat to Multiple Targets (TMT)

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