Application of exercise rehabilitation model based on multidisciplinary collaboration in patients with chronic kidney disease

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2200066832

Enrollment

Unknown

Registered

2022-12-19

Start date

2021-04-30

Completion date

Unknown

Last updated

2023-05-15

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

Conditions

Chronic kidney disease

Interventions

Control group:Routine treatment and nursing in nephrology department, and personalized diet guidance in combination with nutrition department

The experimental group:On the basis of the control group, the MDT exercise rehabilitation team was established, and individualized rehabilitation exercise prescription was formulated

Eligibility

Sex/Gender

All

Age

18 Years to 59 Years

Inclusion criteria

Inclusion criteria: ? All included patients were consistent with Kidney Disease:Improving Global prognosis Outcomes ?-? stage of CKD (15ml/min/1.73m2? glomerular filtration rate (GFR)?59ml/min/1.73m2) and diagnostic criteria in the KDIGO guideline. 18 years old, age ?59 years old, the life expectancy is at least 3 months. (3) Those who are fully informed about this study, voluntarily participate in this study and sign the informed consent form. ? The subjects passed the actual operation examination.

Exclusion criteria

Exclusion criteria: ? The subjects developed persistent hypertension (blood pressure >180/110mmHg) or hypotension (blood pressure 55mmHg), heart failure, unstable angina pectoris, pericardial effusion, etc. Severe metabolic diseases such as hyperthyroidism. Immune system diseases such as myasthenia gravis. Neurological diseases such as cerebral infarction. ? In the past three years, there is any bone and joint injury or surgery, long-term limb pain, joint ankylosis or severe arthritis, affect the test. ? Without mobile phones, wechat or unable to master the use of mobile phones, wechat. ? Cognitive dysfunction or inability to cooperate and mental disorders. ? Participating in other clinical trials that influence the results of this study. The subjects failed to pass the actual operation assessment.

Design outcomes

Primary

Measure	Time frame
grip strength;	—

Secondary

Measure	Time frame
Serum albumin;self-efficacy;quality of life;	—

Countries

China

Contacts

Public ContactXujuan

The First Affiliated Hospital of Xiamen University

13959237709@163.com13959237709

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026