Assessment of Quality of Life in Disorders of the Pelvic Floor

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT01134588

Acronym

U-GYN-QOL

Enrollment

129

Registered

2010-06-02

Start date

2010-05-31

Completion date

2013-01-31

Last updated

2015-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pelvic Organ Prolapse

Brief summary

The purpose of this study is to compare the touch-screen version of the PFDI-20, PFIQ-7, PISQ 12 and SF-36 french questionnaires to their paper versions. The investigators hypothesize that the percentage of completely filled questionnaires will be higher in the touch-screen version.

Interventions

OTHERPaper questionnaire

OTHERTouch screen questionnaire

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

HEALTH_SERVICES_RESEARCH

Masking

NONE

Eligibility

Sex/Gender

FEMALE

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* the patient has pelvic organ prolapse * the patient requires a surgical intervention within the next 4 to 8 weeks * the patient understands and reads french * the patient is affiliated with a social security system * the patient has given consent

Exclusion criteria

* the patient refuses to participate * the patient is under guardianship

Design outcomes

Primary

Measure	Time frame
Presence / absence of a completely filled out questionnaire	6 months post-op

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026