N39.4 R29.6
Conditions
Interventions
Group 1: Standard care for incontinence + digital sensor-based assistance system (intervention group)
Group 2: Standard care for incontinence (controll group)
Group 3: Caregivers (secondary target gro
Sponsors
Hochschule Neubrandenburg
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: moderate to severe incontinence (grade = 2, urinary or urinary and faecal incontinence), consent to study participation
Exclusion criteria
Exclusion criteria: mild form of incontinence (severity grade 1, urinary or urinary and fecal incontinence), refusal to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Emerging falls are the primary endpoint. This is mainly measured using the recognized measuring methods "STRATIFY" and the "Tinetti test". In addition, the fall logs and individual risk factors of the subjects from the nursing documentation are evaluated. The measurements take place every three weeks over a period of four months. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints are: - Cognitive performance (measured with Mini Mental Status Test) - Quality of life (measured with Quality of Life Questionnaire for Multimorbid Elderly (FLQM)) - Sleep quality and sleep disturbances (measured with Karolinska Sleepiness Scale (KSS) & Richard Campbell's Sleep Questionnaire (RCSQ)) - Consumption of incontinence materials (counted) - General state of health (from nursing documentation) The measurements take place every three weeks over a period of four months. | — |
Countries
Germany
Contacts
Public ContactAlexandra Neumann
Hochschule Neubrandenburg
Outcome results
None listed