What is the benefit of biofeedback training of the pelvic floor with ACTICORE1® for urinary incontinence?

Not Applicable

• Conditions: N39.3; N39.4; Stress incontinence; Other specified urinary incontinence

• Registration Number: DRKS00024913
• Lead Sponsor: Oberhavel Klinik Oranienburg

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2021-03-31
• Study Completion: 2023-01-09
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

All urinary incontinent patients with subjective impairment and an ICIQ score of greater than or equal to 5

- Vulnerable individuals are also included: Patients with mental illnesses, People with illnesses or disabilities that impair their ability to understand and / or significantly impair their ability to cope with everyday life; pregnant women, patients under 18 years of age (2-11, 12-17) and> 65 years of age signed informed consent

Exclusion Criteria

Understanding of the patient's participation in the study
- Vulvodynia
- Paraplegic symptoms include traumatic injuries to the nerves and the spinal cord at the cervical, thoracic, lumbar and sacral levels
- Congenital paraplegic symptoms

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
ICIQ-Score 12 weeks after study enrollment