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Strategies for Kidney Outcomes Prevention and Evaluation - The SKOPE Study (SKOPE)

Primary Purpose

Chronic Kidney Diseases

Status
Recruiting
Phase
Not Applicable
Locations
Singapore
Study Type
Interventional
Intervention
Multicomponent intervention
Sponsored by
Duke-NUS Graduate Medical School
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Chronic Kidney Diseases focused on measuring chronic kidney disease, clinical trial, primary care, kidney function

Eligibility Criteria

40 Years - 79 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

4.3 Inclusion Criteria

  • Patients with CKD Stage 3 or Stage 4 defined as persistent reduction in Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) formula eGFR ≥15 and < 60 ml/min/1.73m2 for at least 3 months based on two eGFR readings at least 3 months apart and the last eGFR should be measured at least 3 months ago.
  • Receiving care at the polyclinics in Singapore for at least one year at the time of recruitment
  • Age >=40 and <80 years
  • Singaporean or permanent resident

4.4 Exclusion Criteria

  • On kidney replacement therapy
  • Pregnancy or breastfeeding
  • Known terminal illness
  • Recent hospitalization during last 3 months
  • History of leg or foot ulcers, severe mental illness, prior kidney transplant
  • Inability to provide informed consent

Sites / Locations

  • SingHealth PolyclinicsRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

multicomponent intervention

Usual care

Arm Description

1) 1. Training Nurses/service coordinators as Health Coaches and Hybrid Follow-up Approach of in-person, Telephone and Secure Video Sessions; 2)Training physicians in algorithm-based standardized management of CKD and hybrid care delivery;3) subsidy on sodium-glucose transport protein-2 inhibitors (SGLT-2i) for CKD; and 4) regular CKD case review meetings.

treated by physicians and nurses who are not trained in SKOPE treatment algorithms.

Outcomes

Primary Outcome Measures

the eGFR

Secondary Outcome Measures

Mean change in CVD risk score
measured by The Million Hearts Longitudinal atherosclerotic cardiovascular disease(ASCVD) Risk Assessment score:not assessed via a scale. Results are given as a percent (%) on a scale of less than 1% to 99.99%. A higher score indicates a higher risk
Mean change in CKD quality of life
Assessed by Kidney Disease Quality of Life 36-item short form survey(KDQOL-36TM), score ranges from 0 to 100, higher scores dente better quality of life
Mean change in CKD quality of life
Assessed by The 5-level EuroQol-5D version (EQ-5D-5L):Health state index scores generally range from less than 0 (where 0 is the value of a health state equivalent to dead; negative values representing values as worse than dead) to 1 (the value of full health), with higher scores indicating higher health utility. The second part of the questionnaire consists of a visual analogue scale (VAS) on which the patient rates his/her perceived health from 0 (the worst imaginable health) to 100 (the best imaginable health).

Full Information

First Posted
March 15, 2022
Last Updated
August 10, 2022
Sponsor
Duke-NUS Graduate Medical School
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1. Study Identification

Unique Protocol Identification Number
NCT05295368
Brief Title
Strategies for Kidney Outcomes Prevention and Evaluation - The SKOPE Study
Acronym
SKOPE
Official Title
Strategies for Kidney Outcomes Prevention and Evaluation - The SKOPE Study
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Recruiting
Study Start Date
July 21, 2022 (Actual)
Primary Completion Date
August 2025 (Anticipated)
Study Completion Date
June 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Duke-NUS Graduate Medical School

4. Oversight

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

5. Study Description

Brief Summary
Background: Chronic kidney disease (CKD) is a major public health threat associated with significant morbidity, high mortality, and reduced quality of life. However, empirical evidence is limited on strategies to enhance the effectiveness of care for CKD. The objective of the trial is to evaluate the effectiveness and cost-effectiveness of multicomponent primary care strategies in preserving kidney function among patients with CKD at primary care clinics in Singapore. Methods: A pragmatic, randomized controlled trial, in 4 socioeconomically diverse primary care clinics (polyclinics) in Singapore over 3 years. A total of 896 participants with CKD Stage 3 or worse aged ≥40 and <80 years will be enrolled, with 224 from each polyclinic. Participants enrolled in each polyclinic will be randomly allocated to the intervention or usual care group in a 1:1 ratio. Intervention includes four components 1) training nurses as health coaches for motivational conversation and CKD specific lifestyle counseling on diet and exercise, using hybrid follow-up approach of in-person, telephone, and secure WhatsApp video meetings; 2)Training physicians in algorithm-based standardized management of CKD and hybrid care delivery;3) subsidy on sodium-glucose transport protein-2 inhibitors (SGLT-2i) for CKD; and 4) regular CKD case review meetings. Patients in the usual care arm will be treated by physicians and nurses who and are not trained in SKOPE treatment algorithms. Study outcomes: The primary outcome will be the eGFR total slope from randomization to final follow-up at 36 months. secondary effectiveness outcomes will be 1) Change in CVD risk score as measured by The Million Hearts Longitudinal ASCVD Risk Assessment score 2) Change in CKD quality of life measured by KDQOL-36TM

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Kidney Diseases
Keywords
chronic kidney disease, clinical trial, primary care, kidney function

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
896 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
multicomponent intervention
Arm Type
Experimental
Arm Description
1) 1. Training Nurses/service coordinators as Health Coaches and Hybrid Follow-up Approach of in-person, Telephone and Secure Video Sessions; 2)Training physicians in algorithm-based standardized management of CKD and hybrid care delivery;3) subsidy on sodium-glucose transport protein-2 inhibitors (SGLT-2i) for CKD; and 4) regular CKD case review meetings.
Arm Title
Usual care
Arm Type
No Intervention
Arm Description
treated by physicians and nurses who are not trained in SKOPE treatment algorithms.
Intervention Type
Other
Intervention Name(s)
Multicomponent intervention
Intervention Description
Intervention includes four components 1) training nurses as health coaches for motivational conversation and CKD specific lifestyle counseling on diet and exercise, using hybrid follow-up approach of in-person, telephone, and secure video sessions; 2)Training physicians in algorithm-based standardized management of CKD and hybrid care delivery;3) subsidy on sodium-glucose transport protein-2 inhibitors (SGLT-2i) for CKD; and 4) regular CKD case review meetings.
Primary Outcome Measure Information:
Title
the eGFR
Time Frame
from randomization to final follow-up at 36 months
Secondary Outcome Measure Information:
Title
Mean change in CVD risk score
Description
measured by The Million Hearts Longitudinal atherosclerotic cardiovascular disease(ASCVD) Risk Assessment score:not assessed via a scale. Results are given as a percent (%) on a scale of less than 1% to 99.99%. A higher score indicates a higher risk
Time Frame
at 12, 24, and 36 months from the baseline
Title
Mean change in CKD quality of life
Description
Assessed by Kidney Disease Quality of Life 36-item short form survey(KDQOL-36TM), score ranges from 0 to 100, higher scores dente better quality of life
Time Frame
at 12, 24, and 36 months from the baseline
Title
Mean change in CKD quality of life
Description
Assessed by The 5-level EuroQol-5D version (EQ-5D-5L):Health state index scores generally range from less than 0 (where 0 is the value of a health state equivalent to dead; negative values representing values as worse than dead) to 1 (the value of full health), with higher scores indicating higher health utility. The second part of the questionnaire consists of a visual analogue scale (VAS) on which the patient rates his/her perceived health from 0 (the worst imaginable health) to 100 (the best imaginable health).
Time Frame
at 12, 24, and 36 months from the baseline
Other Pre-specified Outcome Measures:
Title
Incident eGFR <30 ml/min/1.73m2
Time Frame
from randomization to final follow-up at 36 months
Title
Incident eGFR <45 ml/min/1.73m2;
Time Frame
from randomization to final follow-up at 36 months
Title
Incident eGFR <15 ml/min/1.73m2;
Time Frame
from randomization to final follow-up at 36 months
Title
Incident ACR >300 mg/g;
Time Frame
from randomization to final follow-up at 36 months
Title
Incident dialysis
Time Frame
from randomization to final follow-up at 36 months
Title
Rate of MACE (composite of total death, myocardial infarction, coronary revascularization, stroke, and hospitalization because of heart failure
Time Frame
from randomization to final follow-up at 36 months
Title
Mean change in kidney failure risk equation ( KFRE) score
Description
The score is based on an equation not on a scale,Results are given as a percent (%) on a scale of less than 1% to 99.99%. A higher score indicates a higher risk
Time Frame
from randomization to final follow-up at 36 months
Title
Proportion of subjects who experienced albuminuria defined as ACR >30 mg/g
Description
defined as ACR >30 mg/g
Time Frame
from randomization to final follow-up at 36 months
Title
Rate of All-cause mortality
Time Frame
from randomization to final follow-up at 36 months
Title
Rate of CVD deaths
Time Frame
from randomization to final follow-up at 36 months
Title
Rate of hospital admission due to CHD, heart failure, or stroke
Time Frame
from randomization to final follow-up at 36 months
Title
Mean change in Dietary score
Description
Not based on a scale, higher score indicates better outcome
Time Frame
from randomization to final follow-up at 36 months
Title
Mean change in level of physical activity
Description
International Physical Activity Questionnaire (PHAQ): there is no range, higher scores denote higher levels of physical activities
Time Frame
from randomization to final follow-up at 36 months
Title
Mean change in BMI
Time Frame
from randomization to final follow-up at 36 months
Title
Mean change in adherence to antihypertensive
Time Frame
from randomization to final follow-up at 36 months
Title
Mean change in adherence to glucose-lowering medication
Time Frame
from randomization to final follow-up at 36 months
Title
Mean change from baseline in therapeutic intensity score of antihypertensive medication (all and class specific) therapeutic intensity score (summary measure that accounts for the number of medications and the relative doses a patient received)
Description
summary measure that accounts for the number of medications and the relative doses a patient received. Higher scores indicate higher dose.
Time Frame
from randomization to final follow-up at 36 months
Title
Mean change in Framingham risk score
Description
based on an equation, Results are given as a percent (%) on a scale of less than 1% to 99.99%. A higher score indicates a higher risk
Time Frame
from randomization to final follow-up at 36 months
Title
Proportion of subjects with at least 40% decline in baseline eGFR or kidney replacement therapy ( KRT) with mortality
Time Frame
from randomization to final follow-up at 36 months
Title
b) Proportion of subjects with at least 40% decline in baseline eGFR or KRT without mortality
Time Frame
from randomization to final follow-up at 36 months
Title
c) Proportion of subjects with at least 50% decline in baseline eGFR or KRT with mortality
Time Frame
from randomization to final follow-up at 36 months
Title
d) Proportion of subjects with at least 50% decline in baseline eGFR or KRT without mortality
Time Frame
from randomization to final follow-up at 36 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
79 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
4.3 Inclusion Criteria Patients with CKD Stage 3 or Stage 4 defined as persistent reduction in Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) formula eGFR ≥15 and < 60 ml/min/1.73m2 for at least 3 months based on two eGFR readings at least 3 months apart and the last eGFR should be measured at least 3 months ago. Receiving care at the polyclinics in Singapore for at least one year at the time of recruitment Age >=40 and <80 years Singaporean or permanent resident 4.4 Exclusion Criteria On kidney replacement therapy Pregnancy or breastfeeding Known terminal illness Recent hospitalization during last 3 months History of leg or foot ulcers, severe mental illness, prior kidney transplant Inability to provide informed consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Tazeen H. Jafar, MBBS, MPH, FASN
Phone
+65 66012582
Email
tazeen.jafar@duke-nus.edu.sg
Facility Information:
Facility Name
SingHealth Polyclinics
City
Singapore
Country
Singapore
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ngiap Chuan Tan

12. IPD Sharing Statement

Plan to Share IPD
No

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Strategies for Kidney Outcomes Prevention and Evaluation - The SKOPE Study

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