Randomised controlled trial comparing biofeedback training and specific bladder neck effective pelvic floor rehabilitation in stress urinary incontinent women

Randomised controlled trial comparing biofeedback training and specific bladder neck effective pelvic floor rehabilitation in stress urinary incontinent women - PREVENT

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00004218

Enrollment

108

Registered

2013-08-14

Start date

2012-06-10

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

N39.3 N39.42 N81.1

Interventions

Group 1: Vaginal EMG-Biofeedback: 3 months of pelvic floor training 2-3 times per day for 10 min with Periform probe Group 2: Specific bladder neck effective pelvic floor rehabilitation applying perin

three appointments, 30-60 min. Pelvic floor contractions will be practiced followed by integration into daily life.

Eligibility

Sex/Gender

Female

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Motivation to undergo conservative treatment

Exclusion criteria

Exclusion criteria: neurological diseases, inability to understand German

Design outcomes

Primary

Measure	Time frame
Improvement of pelvic floor symptoms /quality of life employing validated pelvic floor questionnaire at all clinical posttherapeutic visits (after 6 weeks, after 6 months, after 1 year)	—

Secondary

Measure	Time frame
Evaluation of pelvic floor pre-contraction, bladder neck elevation, pelvic floor muscle configuration, length of pelvic floor contraction applying perineal ultrasound at all scheduled follow up appointments (after 6 weeks, after 6 months, after 1 year)	—

Countries

Germany

Contacts

Public ContactKaven Baessler

Charité Universitätsmedizin

kaven.baessler@charite.de03084452996

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026