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Shared Decision Making for Choosing renAl Replacement Therapy in Chronic Kidney Disease Patients

Not Applicable
Recruiting
Conditions
Chronic Kidney Disease Stage 5
Interventions
Behavioral: Education
Registration Number
NCT04976166
Lead Sponsor
Seoul National University Hospital
Brief Summary

Shared decision making (SDM) is an approach where clinicians and patients make decisions together using the best available evidence. An understanding of the patient's treatment goals, the advantages and disadvantages of treatment options, and the likelihood of achieving the outcomes are important to patients. International guidelines recommend that all patients with chronic kidney disease (CKD) at pre-dialysis stage should be educated to improve their knowledge and understanding of their condition and to choose the options for renal replacement therapy (RRT).

Despite these recommendations, pre-dialysis educations are often infrequent. Many patients feel unprepared. Wrong or insufficient understanding due to insufficient explanation of treatment can lead to negative emotions. This may lead to a situation in which the patient loses the opportunity to make patient's own choices, resulting in emergency dialysis or dialysis modality that is not suitable for patients. Therefore, this study aims to evaluate whether SDM has an effect on the choice of RRT among CKD patients.

Detailed Description

This study will be conducted as a multicenter, open-label, randomized, pragmatic clinical trial. A total of 1,194 participants with CKD considering RRT will be randomized into 3 groups. Patients in the conventional group will have education using leaflets. Patients in the extensive informed decision making (EIDM) group will receive more detailed education using intensive learning materials than those in the conventional group. Shared decision making (SDM) group patients will have education according to questionnaires of self-assessment items using a self-developed counseling calendar.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
1194
Inclusion Criteria
  • Patients with chronic kidney disease whose nephrologist predicts initiation of renal replacement therapy within 12 months:

    1. Patients with grade 5 of chronic kidney disease [defined as a creatinine-based estimated glomerular filtration rate (eGFR) < 15 ml/dL/1.73m2 at least 2 times at intervals of 2 weeks or longer]
    2. Patients with the cystatin C-based eGFR < 15 ml/dL/1.73m2 at least once if the creatinine-based eGFR does not accurately evaluate the kidney function of patient due to patient characteristics
    3. Patients whose nephrologist require renal replacement therapy within 12 months due to the patient's comorbidities even when the eGFR is 15ml/dL/1.73m2 or higher
  • Patients aged between 19 and 80 years

  • Patients who understand the study

  • Patients who have no permanent access device for long-term maintenance dialysis

Exclusion Criteria
  • Patients who have contraindication to perform peritoneal dialysis due to abdominal surgery
  • Patients whose life expectancy is less than 6 months due to underlying diseases
  • Patients who have enrolled in other clinical trials within 3 months or plan to participate in other clinical trials during this clinical trial period
  • Patients judged by the investigator to be inappropriate for participation in this clinical trial

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Conventional groupEducationVideos and leaflets will be provided. Patients will have education using leaflets for 5 minutes in each hospital at months 0 and 2, respectively.
Shared Decision Making groupEducationVideos, leaflets, and intensive learning materials will be provided. Patients will check self-assessment items, and then have education according to the patients' preference using a self-developed counseling calendar. Patients will have education for more than 10 minutes at months 0 and 2, respectively.
Extensive Informed Decision Making groupEducationVideos, leaflets, and intensive learning materials will be provided. Patients in the EIDM group will receive more informed and detailed education than those in the conventional group. Patients will have education for more than 10 minutes at months 0 and 2, respectively.
Primary Outcome Measures
NameTimeMethod
The ratio of hemodialysis to non-hemodialysis12 months

To compare the proportion of hemodialysis versus non-hemodialysis (peritoneal dialysis and kidney transplantation) treatments among the groups

Secondary Outcome Measures
NameTimeMethod
Patients' evaluation of the SDM process assessed by Shared Decision-Making Questionnaire (SDM-Q-9)Month 0, 2, and 12

The SDM-Q-9 questionnaire is a nine item measure. Items are reported with six response options ranging from 0, "completely disagree", to 5, "completely agree". In this study, six response options were converted into five incremental stages, i.e. "strongly disagree (1)," somewhat disagree (2)," neither disagree nor agree (3)," somewhat agree (4)," strongly agree (5)". To calculate the total scale score, items are summed resulting in a range from 9-45. Higher scores reflect a participant's participation in shared decision making regarding their treatment.

unplanned dialysis12 months

To compare the rate of unplanned dialysis among the groups

Economic efficiency using a cost-utility analysisMonth 2, and 12

The incremental cost-utility ratio (ICUR) is calculated by the ratio of differences in costs and utilities.

Patients' adherence to medication assessed by Morisky 8-item Medication Adherence Scale (MMAS-8)Month 0, 2, and 12

The MMAS-8 is an 8-items questionnaire and the scale included 7 items with yes/no response options and 1 item with a 5-point Likert scale response option. Cumulative score based on 8 items are used to obtain final adherence score ranging from 0 to 8. Adherence is defined accordingly as low (score 0-5), medium (score 6-7) and high (score 8).

Patients' satisfaction assessed by Patient Satisfaction Questionnaire (ZUF-8)Month 0, 2, and 12

The ZUF-8 is an 8-items questionnaire to assess satisfaction in patients using a scale from 1,"poor" to 4,"excellent". Originally, ZUF-8 used a 4-point scale, but in this study, the investigators further extended the scoring system of this questionnaire from four to five incremental stages of perceived satisfaction, i.e. "poor (1)," rather good (2)," good (3)," very good (4)," extraordinary (5)". The minimum value is 8 and the maximum value is 40. Higher scores mean a better outcome.

Trial Locations

Locations (19)

Bundang Seoul National University Hospital

🇰🇷

Seongnam-si, Gyeonggi-do, Korea, Republic of

Kyungpook National University Chilgok Hospital

🇰🇷

Daegu, Korea, Republic of

Daejeon Eulji Medical Center

🇰🇷

Daejeon, Korea, Republic of

Kyungpook National University Hospital

🇰🇷

Daegu, Korea, Republic of

Chonnam National University Hospital

🇰🇷

Gwangju, Korea, Republic of

Dongguk University Ilsan Hospital

🇰🇷

Goyang, Korea, Republic of

Gachon University Gil Medical Center

🇰🇷

Incheon, Korea, Republic of

Pusan National University Hospital

🇰🇷

Pusan, Korea, Republic of

Ewha Woman's University Seoul Hospital

🇰🇷

Seoul, Korea, Republic of

Korea University Guro Hospital

🇰🇷

Seoul, Korea, Republic of

Kyung Hee University Hospital at Gangdong

🇰🇷

Seoul, Korea, Republic of

Samsung Medical Center

🇰🇷

Seoul, Korea, Republic of

Seoul National University Boramae Medical Center

🇰🇷

Seoul, Korea, Republic of

Seoul National University Hospital

🇰🇷

Seoul, Korea, Republic of

The Catholic University of Korea Eunpyeong St. Mary's Hospital

🇰🇷

Seoul, Korea, Republic of

The Catholic University of Korea Seoul St. Mary's Hospital

🇰🇷

Seoul, Korea, Republic of

Ulsan University Hospital

🇰🇷

Ulsan, Korea, Republic of

Severance Hospital

🇰🇷

Seoul, Korea, Republic of

Yonsei University Wonju Severance Christian Hospital

🇰🇷

Wonju, Korea, Republic of

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