Validation of pelvic floor related symptom and Quality of Life questionnaires in Dutch patients.

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON22262

Enrollment

650

Registered

2010-05-28

Start date

2010-06-01

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

urinary incontinence, erectile dysfunction, pelvic organ prolapse, fecal incontinence

Interventions

Dutch version of the questionnaires: 1. Incontinence Impact Questionnaire Short Form (IIQ-7)

2. Urogenital Distress Inventory Short Form (UDI-6)

3. International Index of Erectile Function short form (IIEF-5)

4. Pelvic Floor Distress Inventory Short Form (PFDI-20)

5. Pelvic Floor Impact Questionnaire Short Form (PFIQ-7)

6. Pelvic Organ Prolapse/Urinary Incontinence Sexual Questionnaire Short Form (PISQ-12)

7. Fecal Incontinence Quality of Life Scale (FIQL)

8. Fecal Incontinence Severity Index (FISI).

Eligibility

Inclusion criteria

Inclusion criteria: 1. Aged 18 years or older; 2. Urinary incontinence and/or pelvic organ prolapse (stadium 2 or higher) and/or erectile dysfunction and/or fecal incontinence for at least 3 months.

Exclusion criteria

Exclusion criteria: 1. Malignancy; 2. Demention; 3. Mental retardation.

Design outcomes

Primary

Measure	Time frame
Questionnaires' Psychometric Properties: 1. Reliability: internal consistency; 2. Reproducibility: test-retest reliability; 3. Validity: convergent validity; 4. Responsiveness: sensivity of change.	—

Contacts

Public ContactE. Utomo

's-Gravendijkwal 230, room H-187

e.utomo@erasmusmc.nl+31 (0)10 7030241

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)