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Effect of early postoperative pain management education for high tibial osteotomy patients: a quasi-randomized controlled trial

Not Applicable
Conditions
high tibial osteotomy patient
Registration Number
JPRN-UMIN000037114
Lead Sponsor
Department of Rehabilitation, Fukuoka Rehabilitation Hospital
Brief Summary

After propensity score matching, 52 pairs of patients were extracted. In the intervention group, 46 patients completed the PNE. In total, 44 patients in the intervention group and 52 patients in the control group were analyzed. Five weeks following surgery, the rehabilitation itself had also significantly decreased catastrophizing, and the difference between the two groups had only a small effect size(d=0.44).

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up continuing
Sex
All
Target Recruitment
98
Inclusion Criteria

Not provided

Exclusion Criteria

(1) scheduled for revision arthroplasty surgery (2) unable to or declined to provide consent for study participation (3) had a self-reported diagnosis of inflammatory arthritis (i.e., rheumatoid arthritis, systemic lupus erythematosus, or ankylosing spondylitis) (4) had neurological or psychological disease (5) scheduled to undergo HTO because of a fracture, malignancy, or infection (6) scheduled for bilateral HTO (7) scheduled for unilateral arthroplasty (8) reported plans to undergo hip or knee arthroplasty within 6 months after the current HTO

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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