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Assessment of Quality of Life in Disorders of the Pelvic Floor (U-GYN-QOL)

C

Centre Hospitalier Universitaire de Nīmes

Status

Completed

Conditions

Pelvic Organ Prolapse

Treatments

Other: Touch screen questionnaire
Other: Paper questionnaire

Study type

Interventional

Funder types

Other

Identifiers

NCT01134588
LOCAL/2009/VL-01

Details and patient eligibility

About

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.

Enrollment

129 patients

Sex

Female

Ages

18+ years old

Volunteers

No 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

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

129 participants in 2 patient groups

Reference group
Active Comparator group
Description:
This group will fill out paper questionnaires.
Treatment:
Other: Paper questionnaire
Experimental group
Experimental group
Description:
This group will fill out touch-screen questionnaires.
Treatment:
Other: Touch screen questionnaire

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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