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Application Study of Full-Process Personalised Education and Nursing Combined with the CICARE Communication Model in Enhancing Postoperative Rehabilitation Outcomes Following Unilateral Dual-Channel Spinal Endoscopy

Application Study of Full-Process Personalised Education and Nursing Combined with the CICARE Communication Model in Enhancing Postoperative Rehabilitation Outcomes Following Unilateral Dual-Channel Spinal Endoscopy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600122851
Enrollment
Unknown
Registered
2026-04-20
Start date
2024-07-01
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Lumbar spinal canal disorders following UBE surgery (excluding lumbar spondylolisthesis)

Interventions

Control group :Routine Care Protocol
Intervention group:Nursing Protocol Combining Whole-Process Personalized Education with the CICARE Communication Model

Sponsors

The Third People’s Hospital of Henan Province
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years, conscious and alert; 2. Symptoms manifesting as low back pain with unilateral radiating pain; 3. Patients who have undergone three months of conservative treatment without improvement and are scheduled for UBE surgery; 4. Imaging demonstrating single-level lumbar disc herniation (LDH); 5. Affected segment located at L4-L5 or L5-S1; 6. No prior history of other spinal surgeries; 7. Patients signed an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Lumbar spondylolisthesis; 2. Severe coagulopathy or current oral anticoagulant therapy; 3. Comatose or incapacitated; 4. MRI contraindications (history of endovascular stent implantation, cardiac pacemaker or biostimulator device implantation, etc.); 5. Concurrent severe cardiopulmonary disease, hypertension, psychiatric history, etc.; 6. Patients who withdrew from the study or refused to cooperate.

Design outcomes

Primary

MeasureTime frame
Short-Form McGill Pain Questionnaire (SF-MPQ) Score;General Self-Efficacy Scale;Self-Rating Anxiety Scale (SAS);Self-Rating Depression Scale (SDS);Length of Hospital Stay;Time to Ambulation;Oswestry Disability Index,ODI;Short-Form 36 Health Survey,SF-36;Nursing Satisfaction;

Countries

China

Contacts

Public ContactShina Cheng

The Third People’s Hospital of Henan Province

1245104769@qq.com+86 187 4981 8096

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 1, 2026