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Clinical Trial Details — Status: Completed

Administrative data

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

Study information

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

Clinical Trial Summary

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


Description:

Subjects of the study should conduct a specific training in pelvic floor exercises. They were randomly assigned into 2 groups: Group A only received written instructions for exercises to be performed at home; Group B received written instructions and, in addition, exercises were performed in a 30 minutes weekly session with a physiotherapist guiding them


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Pelvic floor exercises guided by a physiotherapist
Subjects perform two types of contractions of the pelvic floor in two different positions 3 times a day and once a week they check it with a physiotherapist (this day only they do it twice at home)
Non guided pelvic floor exercises
Subjects perform two types of contractions of the pelvic floor in two different positions 3 times a day. They do not attend to meetings with a physiotherapist

Locations

Country Name City State
Spain Hospital General de Villalba Villalba Madrid

Sponsors (2)

Lead Sponsor Collaborator
Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz Universidad Rey Juan Carlos

Country where clinical trial is conducted

Spain, 

References & Publications (5)

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

Outcome

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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