After hip replacement surgery
Conditions
Interventions
conventional rehabilitation group:1. Manual evaluation
2. Traditional consultation model
3. A rehabilitation physician develops a plan based on clinical experience.
Intelligent Rehabilitation Group:1. Therapeutic Decision-Making System
2. Resource Scheduling Platform
3. Intelligent evaluation of the Jukang stack system
Sponsors
The First Affiliated Hospital of Xinxiang Medical University
Eligibility
Sex/Gender
All
Age
40 Years to 75 Years
Inclusion criteria
Inclusion criteria: 1. Meet the treatment indications for hip replacement surgery, as outlined in the "Operational Guidelines for Hip and Knee Replacement Surgery (2022 Edition)"; 2. Postoperative imaging (X-ray) confirmed that the prosthesis was well positioned, with no signs of loosening, dislocation, or infection; 3. Aged 40 to 75, capable of signing or authorizing the signing of an informed consent form; 4. Vital signs are stable, and wounds are healing well; 5. Daily living ability: Barthel index <= 60 points; 6. Motor function: Before surgery, the patient could walk independently, without the need for a walker or with only the assistance of a single crutch.
Exclusion criteria
Exclusion criteria: 1. Merge severe dysfunction of important organs such as the heart, liver, and kidneys or malignant tumors; 2. Previous history of contralateral hip joint surgery or ipsilateral hip joint revision surgery; 3. Occurrence of grade 3 or above treatment-related adverse events (such as fractures, epileptic seizures); 4. Suffering from neurological disorders (such as stroke, Parkinson's disease) or motor dysfunction that affects gait; 5. Previous history of rehabilitation treatment in the same area (which may interfere with the evaluation of effectiveness; 6. There are other joint diseases such as hip joint infection and active rheumatoid arthritis present; 7. Currently participating in other rehabilitation intervention clinical trials; 8. Unable to use smart devices; 9. The researchers' comprehensive analysis suggests that it is not suitable to participate in this study; 10. Pregnant or lactating women.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Rehabilitation Intervention Rate;Utilization Rate of Rehabilitation Resources;Rehabilitation expenditure as a percentage of total medical spending;Efficiency of Rehabilitation Evaluation; | — |
Secondary
| Measure | Time frame |
|---|---|
| Satisfaction Assessment;Adverse Event Incidence Rate;Inpatient Stay Duration (days);Total hospitalization costs (?); | — |
Countries
China
Contacts
Public ContactYazhou Wang
The First Affiliated Hospital of Xinxiang Medical University
Outcome results
None listed