Improving Women's Health by Using an Electronic Pelvic Floor Questionnaire
NCT ID: NCT00880880
Last Updated: 2015-10-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
284 participants
INTERVENTIONAL
2007-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
NONE
Study Groups
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pre-visit e-PAQ-PF
Participants assigned to fill out the e-PAQ-PF prior to their clinic visit. Participants will arrive early to clinic appointment and fill out e-PAQ-PF. Results will be given to clinician and participant. After their visit they will complete the post visit questionnaire.
e-PAQ-PF
Participants will fill out the e-PAQ-PF prior to their clinic visit. The e-PAQ-PF has 4 dimensions (urinary, bowel, vaginal, sexual) and asks about symptoms severity, bother of symptoms, and impact on quality of life. A copy of the results will be given to their clinician and the participant.
post-visit e-PAQ-PF
Participants assigned to complete the e-PAQ-PF after their clinic visit. Pre-visit participants will sign consent form - but otherwise will receive no study interventions. Post-visit they will fill out e-PAQ-PF and post visit questionnaire.
No interventions assigned to this group
Interventions
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e-PAQ-PF
Participants will fill out the e-PAQ-PF prior to their clinic visit. The e-PAQ-PF has 4 dimensions (urinary, bowel, vaginal, sexual) and asks about symptoms severity, bother of symptoms, and impact on quality of life. A copy of the results will be given to their clinician and the participant.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Aged 40 and older
* Scheduled for a well visit at the Women's Health Internal Medicine West Clinic
Exclusion Criteria
* Unable to fill out questionnaire
* Excluded by patient's clinician prior to recruitment
40 Years
FEMALE
Yes
Sponsors
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Sigma Xi Society
UNKNOWN
Agency for Healthcare Research and Quality (AHRQ)
FED
University of Wisconsin, Madison
OTHER
Responsible Party
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Principal Investigators
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Chris M Schussler-Fiorenza, MD
Role: PRINCIPAL_INVESTIGATOR
University of Wisconsin School of Medicine & Public Health
Ronald E Gangnon, PhD
Role: STUDY_CHAIR
University of Wisconsin, Madison
Arnold Wald, MD
Role: PRINCIPAL_INVESTIGATOR
University of Wisconsin School of Medicine & Public Health
Locations
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UW Health Women's Health Internal Medicine West
Madison, Wisconsin, United States
Countries
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References
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Schussler-Fiorenza Rose SM, Gangnon RE, Chewning B, Wald A. Increasing Discussion Rates of Incontinence in Primary Care: A Randomized Controlled Trial. J Womens Health (Larchmt). 2015 Nov;24(11):940-9. doi: 10.1089/jwh.2015.5230.
Other Identifiers
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HS17028
Identifier Type: -
Identifier Source: org_study_id
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