sefulness of biofeedback training with Acticore1 for patients suffering from anal incontinence

Not Applicable

• Conditions: R15; Faecal incontinence

• Registration Number: DRKS00019190
• Lead Sponsor: niversitätsklinik für Allgemein-, Viszeral-, Gefäß- und Transplantationschirurgie

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2019-12-23
• Study Completion: 2021-04-15
• Results First Posted: 2022-04-15
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 37

Inclusion Criteria

patients with faecal inontinence
Wexner score of at least greater than 2
Patients = 18 years
Patients who use a smartphone daily
Signed consent
Also included are vulnerable individuals with mental illnesses, people with illnesses or disabilities that impair their ability to discern and / or significantly impair their ability to cope with everyday life

Exclusion Criteria

pregnancy
vulvdynia
Age <18 years
Rejection of study participation by the patient
open sacral wounds, congential diseases of the
Paraplegic symptoms due to traumatic injuries to the nerves and the spinal cord at the cervical, thoracic, lumbar and sacral levels
- Congenital paraplegic symptoms
- Patients with sacral, perianal open secreting wounds in the Z.n. Resection of rectum and rectum and amputations

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Wexner score after 16 weeks pelvic floor training

Secondary Outcome Measures

Name	Time	Method
quality of life after 16 weeks using EuroQol questionnaire