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A Mobile Application Based Dietary Self Management Intervention in Chinese Chronic Kidney Disease Patients

A Mobile Application Based Dietary Self Management Intervention in Chinese Chronic Kidney Disease Patients: a Multi-Center Randomized Controlled Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04940819
Acronym
CRISS-MADE
Enrollment
9863
Registered
2021-06-28
Start date
2021-06-30
Completion date
2023-06-30
Last updated
2021-06-28

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

Conditions

Chronic Renal Disease

Keywords

Chronic Renal Disease, Dietary Management, Mobile Application

Brief summary

This is a multi-center randomized controlled study. This study aims to investigate the acceptability and efficacy of a newly developed mobile application in the dietary management of chronic kidney disease (CKD) patients.

Detailed description

The prevalence of CKD has reached 10.8% in China. Increasing in prevalence of other non-communicable disease such as hypertension, diabetes and obesity is contributing to this rise in CKD and end-stage renal disease prevalence. Diet is a strong modifiable factor in these diseases. Dietary control is also an integral part in CKD disease self management. However, the complexity in the dietary management of CKD makes it hard for patients to adequately self manage. With the development of smart phone, many mobile applications have been developed to suit the need of patients with chronic diseases. But there has been a scarce of randomized trial to support the feasibility, acceptability and efficacy of these mobile applications. Our study aims to employ a newly developed dietary logging and monitoring application in the primary care setting of CKD patients to test its acceptability and efficacy in disease control. The application is developed by a multidisciplinary team in a tertiary care center. The main features include searching and logging foods, receiving realtime feedback on key nutrient intake levels and facilitating patient-care giving communication. We plan to enroll 14 tertiary hospitals and 42 secondary hospitals in 7 geographical regions in China aiming to reach participants in resource poor areas. Participants will be randomized with 1 to 1 ratio to either receiving mobile application dietary intervention or usual dietary consultation. The planned intervention period is 3 months. We will monitor biochemical parameters relating to dietary control and evaluate patient-centered outcomes concerning CKD self management and control.

Interventions

BEHAVIORALMobile Application for Dietary Management

A mobile application developed by a multi-disciplinary team will be used in the dietary management of CKD patients. The application is patient orientated. It has 4 core features including food searching, dietary logging, personalized key nutrient intake feedback and patient-caregiver interaction.

Sponsors

Peking Union Medical College Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Diagnosed with CKD for more than 3 months * Objective measures of kidney disease (fulfill one of the following): 1) eGFR≤60ml/min/1.73m\^2; 2) Proteinuria (Protein + on dipstick or 24 hour urine protein\>0.3g or albumin-to-creatinine ratio (ACR) \>30mg/mmol or protein-to-creatinine ratio (PCR) \>50mg/mmol); 3) Imaging proven kidney disease (Atrophy, stone formation, cystic kidney disease, or other structural abnormality) * Having access to a mobile phone and is capable of using the dietary intervention application

Exclusion criteria

* Can not provide history of kidney disease or can not provide laboratory result for the past 3 month * Can not use a mobile phone or deemed unfit to participate by their treating nephrologist

Design outcomes

Primary

MeasureTime frameDescription
Change in Self-Efficacy for Managing Chronic Disease Scale3 monthsScore of Self-Efficacy for Managing Chronic Disease Scale (6 items, each measured on a 1-10 likert scale, higher score indicate better self-efficacy) before and after intervention period
Change in Perceived Medical Condition Self-Management Scale (PMCSMS)3 monthsMeasured by Perceived Medical Condition Self-Management Scale (8-item CKD-specific version of the PMCSMS, each item is scored on a 1-5 likert scale, with higher score indicating better self management on item 3/4/5/8 and lower score indicating better self management on item 1/2/6/7) before and after intervention
Dietary Intake3 monthsDietary intake of calorie, protein, sodium, potassium and phosphate evaluated by three-day diet records (3DDR)
Diet Quality3 monthsCalculated by Chinese Healthy Eating Index
Blood Pressure3 monthsMeasure BP in office visits after the intervention period. Changes in antihypertensive medication requirements (total number, dose, class) will be collected from participants and verified with hospital records.
change in estimated Glomerular Filtration Rate (eGFR)3 monthsblood draw (fasting) before and after intervention period
Change in Proteinuria3 monthsspot urine before and after intervention period
Change in Disease Related Quality of life3 monthsMeasured by Kidney Disease Quality of Life 36-Short Form questionnaire

Secondary

MeasureTime frameDescription
Change in the score of Hospital Anxiety and Depression Scale3 monthsMeasured by Hospital Anxiety and Depression Scale (14 items each rated on a 0-3 score, with higher score indicating worse anxiety or depression symptoms) before and after intervention
Change in the score of Generalized Anxiety Disorder Scale3 monthsMeasured by Generalized Anxiety Disorder Scale (a 7-item self-report scale. Items are rated on a 4-point Likert-scale with 0 = not at all to 3 = nearly every day ) before and after intervention
Blood Chemistry (Potassium, Bicarbonate, Phosphate)3 monthsblood draw (fasting) before and after intervention period
Urine Sodium/potassium Ratio3 monthsMeasured by spot urine at baseline and after intervention
Salt Taste Threshold3 monthsSalt taste threshold measured using salt-impregnated test strips before and after the intervention period
Kidney Nutrition Knowledge, Attitude and Practice3 monthsMeasured by self developed questionnaire about knowledge, attitude and practice in kidney disease specified diet
Acceptability of the Application3 monthsMeasured by user acceptability survey and semistructured interviews conducted in participants and nephrologists
Adherence3 monthsTotal number of diet diary logged by participants over complete study period (more than 60% logged is deemed good adherence)
Adoption3 monthsMeasured by percentage of complete dietary log in days will be counted (\>1200kcal deemed as complete log)

Other

MeasureTime frameDescription
Change in Chronic Kidney Disease Self-Efficacy Instrument3 monthsScore of Chronic Kidney Disease Self-Efficacy Instrument before and after intervention period
Change in Kidney Disease Behaviors Inventory3 monthsKidney Disease Behaviors Inventory before and after intervention

Countries

China

Contacts

Primary ContactXixi Zheng, MD
zxxpumch@163.com+8613521145030
Backup ContactPeng Xia, MD
7-xp@163.com+8613811684903

Outcome results

None listed

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