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Research on Rehabilitation Nursing Practice and Intervention Effect after Hip Replacement Surgery Based on Immersive Scene Mode

Research on Rehabilitation Nursing Practice and Intervention Effect after Hip Replacement Surgery Based on Immersive Scene Mode

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600127382
Enrollment
Unknown
Registered
2026-06-30
Start date
2026-07-01
Completion date
Unknown
Last updated
2026-07-13

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

Conditions

Postoperative Rehabilitation of Hip Replacement

Interventions

Experimental group:Immersive Rehabilitation Care
Control group:Routine care

Sponsors

Beijing Bo'ai Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Aged 50 to 80 years old, no gender restriction; 2.Confirmed as hip joint lesions (femoral head necrosis, hip arthritis, hip fracture, etc.) by imaging examination, unilateral hip arthroplasty is planned; 3.No previous hip surgery history and no severe joint deformity; 4.The patient is fully conscious and able to communicate normally, and can cooperate with rehabilitation training and various index tests. There is no severe dysfunction of the heart, liver, kidney, lung and other organs, and no abnormal blood coagulation function; 5.Voluntarily participate in this study and sign the informed consent form; 6.Resides locally and can complete the entire follow-up visit cooperatively.

Exclusion criteria

Exclusion criteria: 1.Patients complicated with severe neurological diseases (such as stroke, Parkinson's disease, multiple sclerosis) who are unable to finish rehabilitation training independently; 2.those with cognitive disorders or mental illnesses (such as depression, schizophrenia) that hinder study cooperation; 3.those suffering from severe postoperative complications including incision infection, prosthesis loosening and dislocation requiring reoperation; 4.patients combined with lower extremity vascular lesions (such as previous deep venous thrombosis), severe osteoporosis, rheumatoid arthritis and other conditions affecting rehabilitation outcomes; 5.those who fail to cooperate with all indicator tests or are expected to lose contact during follow-up; 6.and individuals with contraindications or intolerance to the intervention measures of this study.

Design outcomes

Primary

MeasureTime frame
Harris Hip Function Score;

Secondary

MeasureTime frame
Modified Barthel Index;Complication rate within 6 months after surgery;SF-36 Quality of Life Score 6 Months After Surgery;Patient satisfaction;Post-surgery self-recovery management score;

Countries

China

Contacts

Public ContactZhang Baocui

Beijing Bo'ai Hospital

zhangbaocui0729@sina.com+86 10 87569060

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026