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The efficacy of cognitive behavioral therapy for chronic pain: a pilot study

Phase 1
Conditions
chronic pain
Registration Number
JPRN-UMIN000020880
Lead Sponsor
Faculty of Health Science Naragakuen University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
15
Inclusion Criteria

Not provided

Exclusion Criteria

1. patients who have need medical treatment rapidly 2. patients who have alcohol abuse or drug abuse 3. patients who have mental disease such as hypomania, mania, psychotic disorder 4. patients who have significant suicidal ideation 5. patients who have cognitive dysfunction such as delirium, dementia, mental retardation 6. patients who are difficult to communicate with Japanese 7. patients who have chronic pain because of accident or surgery 8. patients who have compensation or suits 9. patients who select 10 score in numerical rating scale 10. patients who are judged inappropriate to the research by the attending physician

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
EQ-5D-5L Evaluations are performed at baseline, end of the CBT treatment, and 6-month follow-up.
Secondary Outcome Measures
NameTimeMethod
SF-12 Numerical Rating Scale Pain Disability Assessment Scale Patient Health Questionnaire-9 Pain Catastrophizing Scale Tampa Scale for Kinesiophobia eleven Pain Self-Efficacy Questionnaire Keele STarT Back Screening Tool generic condition Somatic Symptom Scale-8
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