Impact of APP-assisted Patient Management on the Quality Control of Blood Purification Therapy

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorYunfeng Xia

About this trial

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.

Eligibility criteria

Qualifiers

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.

Disqualifiers

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.

Trial design

Treatments tested in this trial

  • APP-based management

Treatment groups

392 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Yunfeng Xia

Lead sponsor

First Affiliated Hospital of Chongqing Medical University

Sponsor institution