Clinical trial of individual cognitive Behavioral Therapy for chronic pain (single arm trial)

Not Applicable

• Conditions: Somatic symptom disorder with mainly pain

• Registration Number: JPRN-UMIN000027153
• Lead Sponsor: Chiba University Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2017-04-26
• Study Completion: 2019-03-31
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete: follow-up complete
• Sex: All
• Target Recruitment: 17

Inclusion Criteria

Not provided

Exclusion Criteria

Those who fall under any of the following conditions are not included. 1) Persons who are expected to have cessation of behavioral cognitive therapy due to complications of severe mental disorders such as organic brain disorder, psychotic disorder, bipolar disorder, drug dependence etc due to these symptoms worsening 2) Persons who have mental developmental delay (refer to JART - 25: Japanese Adult Reading Test25) 3) Those with neurocognitive disorders (dementia) (MMSE: refer to evaluation scores by Mini Mental State examination) 4) those with autistic spectrum spectroscopy (AQ: refer to Autism Spectrum Index) 5) Persons who are expected to have cessation of cognitive behavioral therapy because of the danger of impending suicide. 6) Persons who are anticipated to have cessation of cognitive behavioral therapy because they repeat anti-social behavior. 7) Persons who are predictive of cessation of cognitive behavioral therapy because they have significant progressive physical disorder. 8) Persons who are difficult to contact with researchers. 9) Other persons who are judged inappropriate for the examination responsible doctor or the test sharing psychologist to safely carry out this test.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1.Numerical Rating Scale (NRS) 2.Pain Catastrophizing Scale (PCS) (Both are evaluated after 16 weeks.)

Secondary Outcome Measures

Name	Time	Method
After 8 weeks, 1.Numerical Rating Scale (NRS) 2.Pain Catastrophizing Scale (PCS) After 16 weeks, 3.Pain Disability Assessment Scale (PDAS) 4.PHQ-9(Patient Health Questionnare-9) 5.GHQ-7(Generalized anxiety disorder-7) 6.EQ-5D-5L(EuroQol5-Dimension-5Levels)