Regaining Bladder Control in Postmenopausal Women With Osteoporosis

This study has been completed.
Sponsor:
Information provided by:
University of British Columbia
ClinicalTrials.gov Identifier:
NCT00323245
First received: May 8, 2006
Last updated: April 12, 2011
Last verified: April 2011
  Purpose

Conservative management for urinary incontinence has been shown to improve bladder control. We are conducting a study of the effectiveness of conservative management for urinary incontinence in women who also have osteoporosis. We hope to find that treatment for incontinence improves bladder control and thereby allows women to be more active and reduces their risk of falling and breaking bones.


Condition Intervention
Urinary Incontinence
Behavioral: Physiotherapy for urinary incontinence

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind (Subject)
Primary Purpose: Treatment
Official Title: Regaining Urinary Continence in Postmenopausal Women With Osteoporosis: A Randomized Controlled Trial.

Resource links provided by NLM:


Further study details as provided by University of British Columbia:

Primary Outcome Measures:
  • Number of Incontinent Episodes (baseline and end of treatment (12 weeks) [ Time Frame: Unspecified ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Urinary Distress Inventory [ Time Frame: Unspecified ] [ Designated as safety issue: No ]
  • Pelvic Floor Muscle Strength [ Time Frame: Unspecified ] [ Designated as safety issue: No ]
  • Quality of life: Each participant will complete the Incontinence Impact Questionnaire and the SF-36 at the initial and follow up measurement sessions [ Time Frame: Unspecified ] [ Designated as safety issue: No ]
  • Physical Activity (PASE) [ Time Frame: Unspecified ] [ Designated as safety issue: No ]
  • 24 Hour Pad Test [ Time Frame: Unspecified ] [ Designated as safety issue: No ]
  • Voiding Frequency using the bladder diary [ Time Frame: Unspecified ] [ Designated as safety issue: No ]
  • Spinal Curvature with a flexicurve ruler [ Time Frame: Unspecified ] [ Designated as safety issue: No ]
  • Self-Perceived Efficacy [ Time Frame: Unspecified ] [ Designated as safety issue: No ]
  • All at initial and follow up (end) measurement sessions [ Time Frame: Unspecified ] [ Designated as safety issue: No ]

Estimated Enrollment: 48
Study Start Date: March 2006
Study Completion Date: April 2011
Primary Completion Date: April 2011 (Final data collection date for primary outcome measure)
Intervention Details:
    Behavioral: Physiotherapy for urinary incontinence
    See Detailed Description.
  Eligibility

Ages Eligible for Study:   55 Years to 80 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

Postmenopausal women osteopenia or osteoporosis and stress urinary incontinence

Exclusion Criteria:

-

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00323245

Locations
Canada, British Columbia
BC Womens' Health Centre
Vancouver, British Columbia, Canada
Sponsors and Collaborators
University of British Columbia
Investigators
Principal Investigator: Meena Sran, PT, PhD The University of British Columbia
  More Information

No publications provided

Responsible Party: Dr. Meena Sran, University of British Columbia
ClinicalTrials.gov Identifier: NCT00323245     History of Changes
Other Study ID Numbers: C05-0608, W05-0259
Study First Received: May 8, 2006
Last Updated: April 12, 2011
Health Authority: Canada: Health Canada

Keywords provided by University of British Columbia:
Randomized clinical trial
osteoporosis
urinary incontinence
physiotherapy
education

Additional relevant MeSH terms:
Osteoporosis
Urinary Incontinence
Bone Diseases, Metabolic
Bone Diseases
Musculoskeletal Diseases
Urination Disorders
Urologic Diseases
Urological Manifestations
Signs and Symptoms

ClinicalTrials.gov processed this record on April 16, 2014