The efficacy of the cognitive behavioral therapy for overactive bladder in women: a randomized controlled trial
Not Applicable
- Conditions
- Overactive bladder
- Registration Number
- JPRN-UMIN000038513
- Lead Sponsor
- Department of Urology, Kyoto University, Graduate School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Female
- Target Recruitment
- 79
Inclusion Criteria
Not provided
Exclusion Criteria
1. Participants has abnormality around the bladder (e.g., bladder stone, urethral stone, interstitial cystitis, endometriosis, pelvic organ prolapse). 2. Participant is diagnosed as Urinary Tract Infection (UTI). 3. Participants who have had surgery for urinary incontinence. 4. Pregnant or possibly pregnant participants. 5. Participants who can not understand the notation of Japanese. 6. Participants with depressed tendency. 7. Participants who are diagnosed as dementia. 8. Participants who are considered as inappropriate for this study by the responsible doctor
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method HRQoL total score of Overactive bladder questionnaire (OAB-q)
- Secondary Outcome Measures
Name Time Method 1. The other score of Overactive bladder questionnaire (OAB-q) 2. Overactive bladder symptom score (OABSS) 3. King's health questionnaire (KHQ) 4. Patient Global Impression-Improvement (PGI-I) 5. Patient Global Impression-Severity (PGI-S) 4. Euroqol-5D-5L (EQ-5D-5L) 5. Hospital Anxiety and Depression Scale (HADS) 6. Frequency volume chart 7. Participant satisfaction 8. Change of drug therapy 9. Adherence of treatment 10. Drop-out rate 11. Adverse events 12. Participant feedback