Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

Assessment of Pelvic Floor Function in Elderly

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT00765622
Recruitment Status : Completed
First Posted : October 3, 2008
Last Update Posted : October 3, 2008
Sponsor:
Information provided by:
Catholic University of Brasília

Tracking Information
First Submitted Date October 2, 2008
First Posted Date October 3, 2008
Last Update Posted Date October 3, 2008
Study Start Date April 2007
Actual Primary Completion Date November 2007   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures
 (submitted: October 2, 2008)
All patients were submitted for review physiotherapeutic through palpation bidigital and quantification of contraction pelvic, was performed using a my feedback of pressure [ Time Frame: Only one measure at the begging of the study ]
Original Primary Outcome Measures Same as current
Change History No Changes Posted
Current Secondary Outcome Measures Not Provided
Original Secondary Outcome Measures Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title Assessment of Pelvic Floor Function in Elderly
Official Title Assessment of Pelvic Floor Function in Women With Urinary Incontinence
Brief Summary The purpose of this study is to demonstrate the importance of functional assessment of the pelvic floor (AFA) in older women, as prognostic factor for Urinary Incontinence (UI).
Detailed Description Incontinence elderly assessment
Study Type Observational
Study Design Observational Model: Case-Crossover
Time Perspective: Cross-Sectional
Target Follow-Up Duration Not Provided
Biospecimen Retention:   Samples Without DNA
Description:
Women
Sampling Method Probability Sample
Study Population elderly women
Condition Urinary Incontinence
Intervention Not Provided
Study Groups/Cohorts
  • G2
    G2 = control group (no incontinence)
  • G1
    G1 = urinary incontinence
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status Completed
Actual Enrollment
 (submitted: October 2, 2008)
153
Original Actual Enrollment Same as current
Actual Study Completion Date November 2007
Actual Primary Completion Date November 2007   (Final data collection date for primary outcome measure)
Eligibility Criteria

Inclusion Criteria:

  • Elderly women
  • Urinary incontinence

Exclusion Criteria:

  • Cesarean surgery
Sex/Gender
Sexes Eligible for Study: Female
Ages 58 Years to 87 Years   (Adult, Older Adult)
Accepts Healthy Volunteers Yes
Contacts Contact information is only displayed when the study is recruiting subjects
Listed Location Countries Brazil
Removed Location Countries  
 
Administrative Information
NCT Number NCT00765622
Other Study ID Numbers ucb123cestari
Has Data Monitoring Committee Yes
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement Not Provided
Responsible Party Ricardo Jacó de Oliveira, Catholic University of Brasilia
Study Sponsor Catholic University of Brasília
Collaborators Not Provided
Investigators
Principal Investigator: Claudia EC Souza, Ms Catholic University of brasilia
PRS Account Catholic University of Brasília
Verification Date August 2008