Impact of APP-assisted Patient Management on the Quality Control of Blood Purification Therapy
1 other identifier
interventional
392
1 country
1
Brief Summary
Many maintenance hemodialysis (MHD) patients develop negative outlooks due to their illnesses and complications, making their quality of life and prognosis a clinical concern. Effective life management and treatment cooperation are crucial to improving dialysis quality and patient outcomes. This trial aims to evaluate whether management through the "Yueya" mini-program and WeChat can provide personalized guidance such as health education, diet, exercise, medication supervision, and condition monitoring to enhance treatment compliance, quality of life, strengthen quality control in the hemodialysis unit, and improve patient prognosis. Patients will be divided into a group receiving support via the "Yueya" mini-program and WeChat, and a control group receiving routine care. Clinical and laboratory indicators, cardiovascular events, death, hospitalization, quality of life, and compliance will be recorded and compared between groups to assess the impact of APP-assisted patient management on the quality of MHD blood purification therapy and the prognosis of MHD patients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Sep 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 18, 2025
CompletedStudy Start
First participant enrolled
September 22, 2025
CompletedFirst Posted
Study publicly available on registry
December 18, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2026
December 18, 2025
October 1, 2025
1.3 years
September 18, 2025
December 5, 2025
Conditions
Outcome Measures
Primary Outcomes (4)
mortality rate
In this study, mortality rate was used as a prognostic indicator.
About 1 year
Hospitalization rate
In this study, the hospitalization rate was used as a prognostic indicator.
About 1 year
Kidney Disease Quality of Life
Measuring the quality of life of hemodialysis patients through the Kidney Disease Quality of Life-36(KDQOL-36) scale. If the KDQOL-36 score increases, the quality of life is considered to be improved.
About 1 year
Incidence of cardiovascular events
About 1 year
Study Arms (2)
APP management group
EXPERIMENTALFor the APP management group, according to the specific conditions of patients such as age, gender, primary disease and complications, the "Yueya" mini-program and WeChat will be used to provide individualized and all-weather guidance for dialysis patients in their daily lives, including health knowledge education, diet and exercise guidance, medication supervision, condition monitoring and real-time feedback.
Non-APP management group
NO INTERVENTIONFor the non-APP management group, the APP mini-program will not be used to guide patients' daily lives, and only the previous routine management methods will be adopted.
Interventions
Based on patients' specific conditions such as age, gender, primary disease, and complications, the APP-based management will provide individualized and round-the-clock guidance for dialysis patients in their daily lives through the "Yueya" mini-program and WeChat. This guidance covers various aspects, including health knowledge education, diet and exercise guidance, medication supervision, condition monitoring, and real-time feedback.
Eligibility Criteria
You may qualify if:
- Patients with stage 5 chronic kidney disease, who have received maintenance hemodialysis for more than 3 months, are aged between 18 and 75 years old, and have regular dialysis three times a week.
- Patients with relatively stable condition, who are able to take care of themselves and willing to cooperate with the study.
- Patients who can understand and proficiently use WeChat and the "Yueya" mini - program used in this study.
You may not qualify if:
- Patients with communication barriers or other conditions that prevent them from cooperating with the study.
- Patients who have a history of acute myocardial infarction, cerebral infarction or intracerebral hemorrhage in the past six months.
- Patients who are not willing to actively cooperate with the study.
- Patients with severe liver cirrhosis, active tuberculosis and AIDS.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Yunfeng Xialead
Study Sites (1)
The First Affiliated Hospital of Chongqing Medical University
Chongqing, Chongqing Municipality, 400016, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Cheif physician
Study Record Dates
First Submitted
September 18, 2025
First Posted
December 18, 2025
Study Start
September 22, 2025
Primary Completion (Estimated)
December 31, 2026
Study Completion (Estimated)
December 31, 2026
Last Updated
December 18, 2025
Record last verified: 2025-10