Urinary Incontinence Clinical Trial
Official title:
Assessment of the Effectiveness of Guided by a Physiotherapist Versus Non-guided Pelvic Floor Exercises for Urinary Incontinence (UI) in Patients With Relapsing-Remitting (RR) Multiple Sclerosis
NCT number | NCT03000647 |
Other study ID # | EC 65-15 HGV |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | October 2015 |
Est. completion date | October 2016 |
Verified date | March 2018 |
Source | Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The aim of the study is to evaluate the effectiveness of guided versus non guided pelvic floor exercises for urinary incontinence in patients with Relapsing-Remitting Multiple Sclerosis
Status | Completed |
Enrollment | 48 |
Est. completion date | October 2016 |
Est. primary completion date | October 2016 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: 1. Diagnosed with Relapsing-Remitting Multiple Sclerosis 2. Diagnosed with Urinary Incontinence 3. Minimental Sate Examination (MMSE) scale: More than 24 4. Expanded Disability Status Scale (EDSS) scale: Bladder function 0-4; EDSS 0-6,5 5. Willing to participate in the study 6. Having Signed an informed consent Exclusion Criteria: 1. Diagnosed with another neurological disease 2. Diagnosed with kidney diseases 3. Having a Relapse of the disease in the last 6 months 4. In Women: Pregnancy os postpartum < 6 months 5. Having gone through surgery for urinary incontinence or prolapses or prostate diseases 6. Having gone through other treatment for pelvic floor 7. MMSE scale: Under 24 8. EDSS scale: Bladder function 5-6 or not knowing; EDSS 7-10 9. ICIQ-SF scale: Severity 19-21 10. Not willing to participate or sign the informed consent form or not able to understand the study |
Country | Name | City | State |
---|---|---|---|
Spain | Hospital General de Villalba | Villalba | Madrid |
Lead Sponsor | Collaborator |
---|---|
Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz | Universidad Rey Juan Carlos |
Spain,
De Ridder D, Vermeulen C, Ketelaer P, Van Poppel H, Baert L. Pelvic floor rehabilitation in multiple sclerosis. Acta Neurol Belg. 1999 Mar;99(1):61-4. — View Citation
Gilpin SA, Gilpin CJ, Dixon JS, Gosling JA, Kirby RS. The effect of age on the autonomic innervation of the urinary bladder. Br J Urol. 1986 Aug;58(4):378-81. — View Citation
Litwiller SE, Frohman EM, Zimmern PE. Multiple sclerosis and the urologist. J Urol. 1999 Mar;161(3):743-57. Review. Erratum in: J Urol 1999 Jul;162(1):172. — View Citation
Lúcio AC, Campos RM, Perissinotto MC, Miyaoka R, Damasceno BP, D'ancona CA. Pelvic floor muscle training in the treatment of lower urinary tract dysfunction in women with multiple sclerosis. Neurourol Urodyn. 2010 Nov;29(8):1410-3. doi: 10.1002/nau.20941. — View Citation
Quarto G, Autorino R, Gallo A, De Sio M, D'Armiento M, Perdonà S, Damiano R. Quality of life in women with multiple sclerosis and overactive bladder syndrome. Int Urogynecol J Pelvic Floor Dysfunct. 2007 Feb;18(2):189-94. Epub 2006 May 13. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Decrease in the number of urinary leakages from baseline | Difference in the mean number of leakages (Registered for 3 days with a bladder diary) | 12 weeks | |
Secondary | Decrease of urinary incontinence severity from baseline | Comparison of the results: Questions 1, 2 and 3 of the International Consultation on Incontinence Questionnaire (ICIQ-SF) between the group 1 and 2 | 4,8 and 12 weeks | |
Secondary | Change in quality of life from baseline | Comparison of the results (Question 3 of the questionnaire ICIQ-SF and second part (13 questions) of the Overactive Bladder questionnaire (OABQ-SF) between the group 1 and 2 | 4,8 and 12 weeks | |
Secondary | Decrease in the number of urinary leakages from baseline | Comparison of the results (Registered for 3 days with a bladder diary) between the group 1 and 2 | 4 and 8 weeks | |
Secondary | Lower urinary tract symptoms from baseline | Comparison of de results (First part (6 questions) of the questionnaire OABQ-SF) between the group 1 and 2 | 4,8 and 12 weeks | |
Secondary | Adherence | Comparison of the results (Registered with exercise diary)between the group 1 and 2 | 12 weeks |
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