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Behavioral Intervention Program and Vaginal Cones on SUI

NCT01628991 · Status: COMPLETED · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2012-06-27

No results posted yet for this study

Summary

This study is a single blind randomized clinical trial to compare the efficacy of a behavioral intervention program versus vaginal cones on Stress Urinary Incontinence (SUI).

Conditions

  • Stress Urinary Incontinence

Interventions

BEHAVIORAL

behavioural program

interventional behavioural program

DEVICE

Iranian version of vaginal cones

intravaginal device(vaginal cone) for promote the pelvic floor exercises

Sponsors & Collaborators

  • Mashhad University of Medical Sciences

    lead OTHER

Principal Investigators

  • Nahid golmakani, M.Sc. · Mashhad university of medical science, faculty of nursing and midwifery, Mashhad, Iran

  • Nayereh khadem, M.D. · Mashhad university of medical science, Mashhad, Iran

  • Arezoo Arabipoor, M.Sc. · Mashhad university of science, faculty of nursing and midwifery, Mashhad, Iran

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
25 Years
Max Age
65 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-04-30
Primary Completion
2009-08-31
Completion
2009-08-31

Countries

  • Iran

Study Locations

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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 NCT01628991 on ClinicalTrials.gov