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Clinical Effectiveness of MyNutriKidney®

Clinical Effectiveness of MyNutriKidney® for Dietary Self-management in Chronic Kidney Disease Patients: Protocol for a Pragmatic Randomized Controlled Trial

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06956872
Enrollment
200
Registered
2025-05-04
Start date
2025-07-01
Completion date
2027-02-01
Last updated
2025-05-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Kidney Disease, Chronic Kidney Disease Stage 3, Chronic Kidney Disease Stage 4, Chronic Kidney Disease Stage 5

Keywords

MyNutriKidney, chronic kidney disease, CKD, Dietary Adherence, Nutrition Literacy, Self-management, Mobile Health, Dietitian, mHealth, Telemedicine, Digital Health, Malaysia, Kidney Diseases

Brief summary

This study is a 6-month, pragmatic, multi-center, sequentially recruited, stratified, open-label randomized controlled trial (RCT) conducted in Malaysia. It aims to determine the clinical effectiveness of a culturally adapted, gamified mobile health app (MyNutriKidney®) supplementing standard care, compared to standard care alone, for improving dietary self-management among 200 adults with Chronic Kidney Disease (CKD) stages 3-5. Participants will be randomly assigned (1:1, stratified by age and education) into either (i) the intervention group (MyNutriKidney® app + standard care) or (ii) the control group (standard care, including routine dietary counseling and printed materials). The co-primary outcomes are changes in Dietary Adherence (measured by CKD Diet Score) and Nutrition Literacy (measured by NLS score) from baseline to 6 months.

Detailed description

General Objective: To evaluate the clinical effectiveness of supplementing standard care with the MyNutriKidney® mobile application compared to standard care alone in improving dietary adherence and nutrition literacy among patients with Chronic Kidney Disease (CKD) stages 3-5 in Malaysia over a 6-month period. Specific Objectives: 1. To compare the change in Dietary Adherence (DA), assessed by the CKD Diet Score (derived from 3x 24-hour dietary recalls), from baseline to 6 months between the MyNutriKidney® intervention group and the standard care control group. (Co-primary objective) 2. To compare the change in Nutrition Literacy (NL), assessed by the Nutrition Literacy Scale (NLS) score, from baseline to 6 months between the intervention and control groups. (Co-primary objective) 3. To compare the changes in secondary outcomes from baseline to 6 months between the two groups, including: 3.1. Dietary Knowledge, assessed by the Dietary Knowledge Questionnaire (DKQ) score. 3.2. Kidney Function, assessed by the estimated Glomerular Filtration Rate (eGFR). 3.3. Serum Electrolyte Levels (Potassium, Phosphorus, Sodium, Calcium). 4. To evaluate app engagement metrics (e.g., meal logging frequency, time spent on educational resources, challenge completion) among participants in the MyNutriKidney® intervention group over the 6-month period. (Exploratory objective) 5. To assess participant satisfaction and usability of the MyNutriKidney® app using the Malay version of the mHealth Application Usability Questionnaire (M-MAUQ) at 6 months among participants in the intervention group. (Exploratory objective)

Interventions

OTHERCounseling

Subjects in the both arms will receive individualized dietetic counseling as the standard dietetic care in Malaysia

Individualized dietetic counseling aided with a newly developed renal diet app for educative purpose and aiding tool to enhance the dietary adherence among CKD patients. Training on the use of the app will be provided to the subjects prior to the commencement of the intervention. Subjects will be trained on the use of the home screen, icons, feedback screens, the process of entering dietary and fluid intake data and selecting portion sizes. Subjects are considered as competent users when they could correctly record the foods and drinks with correct portion size eaten in the past 24 hours and successfully save the data.

After the counseling session, a standardized renal nutrition pamphlet prepared by dietitians from Universiti Putra Malaysia and Hospital Serdang will be given for patient's educative purpose. Since the mobile application is intended for patient's education and self-monitoring (food diary) purposes, and thus, to ensure the comparability between intervention and control groups, the patients in control group will be trained to record their diet intakes manually using the recommended approach 3-day diet records. Nutritional feedback or advices on the diet records will be given to the participants during follow up sessions.

Sponsors

International Society of Nephrology
CollaboratorOTHER
Universiti Putra Malaysia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Participants must meet all of the following inclusion criteria and none of the

Exclusion criteria

to be eligible for enrolment into the study. Inclusion Criteria: 1. Clinically diagnosed Chronic Kidney Disease (CKD): 1.1. eGFR \< 60 ml/min/1.73m² for ≥ 3 months (applicable to pre-dialysis patients, Stages 3-5) 2. Aged 18 years or older. 3. Possesses a personal smartphone compatible with the MyNutriKidney® application and is willing to use the health app if randomized to the intervention group. 4. Alert and oriented, and deemed capable of providing informed consent and participating in study procedures. 5. Able to communicate and understand study procedures in English, Bahasa Melayu, or Mandarin.

Design outcomes

Primary

MeasureTime frameDescription
Change in Dietary Adherence ScoreChange from Baseline (Month 0) to 6 Months (Month 6).Dietary Adherence (DA) quantified using CKD Diet Score (adapted from GCKD study). Intake data from 3x 24-hour dietary recalls (dietitian interview) per assessment (Baseline, M3, M6). Nutrient intake analyzed. Score derived from 6 components: sodium, potassium, fiber, total protein, sugar, cholesterol. Intake adjusted per 1000 kcal; points 1 (poor) to 5 (high adherence) assigned based on thresholds. Sodium and total protein scores weighted x1.5. Total Score = (Sodium Score 1.5) + Potassium Score + Fiber Score + (Protein Score 1.5) + Sugar Score + Cholesterol Score. Total score range: 7 (poorest adherence) to 35 (highest adherence).
Change in Nutrition Literacy ScoreChange from Baseline (Month 0) to 6 Months (Month 6).Nutrition Literacy assessed using the Nutrition Literacy Scale (NLS) score (validated Malay version). The standardized index score ranges from 0 (lowest literacy) to 100 (highest literacy).

Secondary

MeasureTime frameDescription
Change in Serum Albumin LevelChange from Baseline (Month 0) to 6 Months (Month 6).Serum Albumin level extracted from routine clinical laboratory results. Units measured according to local laboratory standards (e.g., g/L).
Change in Hemoglobin LevelChange from Baseline (Month 0) to 6 Months (Month 6).Hemoglobin level extracted from routine clinical laboratory results. Units measured according to local laboratory standards (e.g., g/dL).
Change in Serum Potassium LevelChange from Baseline (Month 0) to 6 Months (Month 6).Serum potassium (K) level extracted from routine clinical laboratory results obtained near the study visit time points as part of standard CKD care. Unit: mmol/L.
Change in Serum Phosphorus LevelChange from Baseline (Month 0) to 6 Months (Month 6).Serum phosphorus (P) level extracted from routine clinical laboratory results obtained near the study visit time points as part of standard CKD care. Unit: mmol/L.
Change in Serum Sodium LevelChange from Baseline (Month 0) to 6 Months (Month 6).Serum sodium (Na) level extracted from routine clinical laboratory results obtained near the study visit time points as part of standard CKD care. Unit: mmol/L.
Change in Corrected Serum Calcium LevelChange from Baseline (Month 0) to 6 Months (Month 6).Corrected serum calcium (Ca) level extracted from routine clinical laboratory results obtained near the study visit time points as part of standard CKD care. Unit: mmol/L.
Change in Dietary Knowledge ScoreChange from Baseline (Month 0) to 6 Months (Month 6).Dietary Knowledge assessed using the Dietary Knowledge Questionnaire (DKQ) score (25 items). Score is expressed as a percentage (0-100%), with higher scores indicating greater knowledge
Change in Estimated Glomerular Filtration Rate (eGFR)Change from Baseline (Month 0) to 6 Months (Month 6)eGFR calculated using the CKD-EPI formula based on serum creatinine levels extracted from routine clinical laboratory results. Measured in mL/min/1.73 m².

Other

MeasureTime frameDescription
Total Number of Gamification Challenges CompletedCalculated as a total over the period from Baseline (Month 0) to 6 Months (Month 6).Completion of gamification challenges, measured as the total number completed, derived from passively logged user interaction data from the MyNutriKidney® app's backend analytics system. Unit: count. (Assessed in Intervention Group only).
Interaction Rate with Actionable RemindersCalculated over the period from Baseline (Month 0) to 6 Months (Month 6)Responsiveness to notifications, measured as the interaction rate with actionable reminders, derived from passively logged user interaction data from the MyNutriKidney® app's backend analytics system. (Number of Interactions / Number of Reminders Sent) \* 100%. Unit: %. (Assessed in Intervention Group only).
Average Weekly Meal Logging FrequencyCalculated as an average over the period from Baseline (Month 0) to 6 Months (Month 6).Frequency of meal logging, calculated as average logs per week, derived from passively logged user interaction data from the MyNutriKidney® app's backend analytics system. Unit: logs/week. (Assessed in Intervention Group only).
Average Weekly Time on Educational ModulesCalculated as an average over the period from Baseline (Month 0) to 6 Months (Month 6).Time spent interacting with educational modules, calculated as average minutes per week, derived from passively logged user interaction data from the MyNutriKidney® app's backend analytics system. Unit: minutes/week. (Assessed in Intervention Group only).
App Usability and Satisfaction ScoreAssessed at 6 Months (Month 6).Assessed using the Malay version of the mHealth Application Usability Questionnaire (M-MAUQ). An overall average score is calculated based on a 7-point Likert scale (1=strongly disagree to 7=strongly agree), with higher scores indicating better usability/satisfaction. (Assessed in Intervention Group only).

Countries

Malaysia

Contacts

Primary ContactZulfitri 'Azuan bin Mat Daud, Dietitian Lecturer [Dr]
zulfitri@upm.edu.my+60-397692431
Backup ContactLeong Sim Kian, Dietitian
+60-172946309

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026