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The effect of cognitive behavioral intervention on postoperative fear of movement in patients with osteoporotic vertebral compression fractures

The effect of cognitive behavioral intervention on postoperative fear of movement in patients with osteoporotic vertebral compression fractures

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400088765
Enrollment
Unknown
Registered
2024-08-26
Start date
2024-01-01
Completion date
Unknown
Last updated
2024-09-02

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

Conditions

Postoperative fear of movement in patients with osteoporotic vertebral compression fractures

Interventions

control group:The control group received routine nursing interventions, including rest and dietary guidance, psychological care, and rehabilitation training and health education.
Intervention group:(1) Assess the patients cognitive recognition and automatic thinking 24 hours after surgery to set exercise goals and identify the reasons for the patients development of ADHD. (2)

Sponsors

Yuxi People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Those who meet the diagnostic criteria for OVCF in the Expert Consensus on the Diagnosis and Treatment of Osteoporosis Vertebral Compression Fractures (2021 Edition), have been diagnosed through CT and X-ray examinations, and have undergone vertebroplasty for the first time; 2. Within 24 hours after surgery, a score of over 37 points was assessed using the fear of movement scale; 3. Those who voluntarily participate in this study and sign a written informed consent form.

Exclusion criteria

Exclusion criteria: 1. Lack of awareness or cognitive and communication barriers, unable to cooperate with research; 2. Patients with combined pelvic and lower limb fractures; 3. Patients with combined malignant tumors; 4. Individuals with a history of concomitant lower limb venous thrombosis or primary thrombotic disease; 5. Patients who are currently participating in other studies.

Design outcomes

Primary

MeasureTime frame
Fear level;Anxiety and depression levels;Pain level;self-care ability;

Countries

China

Contacts

Public ContactYunye Wang

Yuxi People's Hospital

137250828@qq.com+86 138 3742 3192

Outcome results

None listed

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