Continence Across Continents to Upend Stigma and Dependency

NCT01858493 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 910

Last updated 2017-07-24

No results posted yet for this study

Summary

To determine whether women exposed to the continence promotion intervention will report improved urinary symptoms and quality of life, and lower incontinence-related stigma and falls than women who receive a control intervention at one-year post-intervention.

Conditions

Interventions

BEHAVIORAL

Continence promotion group education workshop

Interactive group education workshop promoting continence

BEHAVIORAL

Sham health lecture

Interactive group education workshop about general health

Sponsors & Collaborators

  • Fonds de la Recherche en Santé du Québec

    collaborator OTHER_GOV
  • Medical Research Council

    collaborator OTHER_GOV
  • Canadian Institutes of Health Research (CIHR)

    collaborator OTHER_GOV
  • Institut national de prevention et d'education pour la sante

    collaborator OTHER_GOV
  • Centre de Recherche de l'Institut Universitaire de Geriatrie de Montreal

    lead OTHER

Principal Investigators

  • Cara Tannenbaum, MD. MSc · Univeristé de Montréal

  • Adrian Wagg, MD · University of Alberta

  • Eleanor van den Heuvel, PhD · Brunel University

  • Xavier Fritel, MD, PhD · University of Poitiers

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
65 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-05-31
Primary Completion
2017-07-31
Completion
2017-07-31

Countries

  • Canada
  • France
  • United Kingdom

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01858493 on ClinicalTrials.gov