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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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German Clinical Trials Register |
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Last refreshed on:
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8 April 2024 |
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Main ID: |
DRKS00007973 |
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Date of registration:
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20/04/2015 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Promoting urinary continence in people with Parkinson’s disease
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Scientific title:
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Promoting urinary continence in people with Parkinson’s disease
- Park-UK |
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Date of first enrolment:
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15/06/2015 |
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Target sample size:
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50 |
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Recruitment status: |
Complete |
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URL:
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http://drks.de/search/en/trial/DRKS00007973 |
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Study type:
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interventional |
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Study design:
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Allocation: Non-randomized controlled study; Masking: Blinded (masking used); Control: active; Assignment: other; Study design purpose: other
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Phase:
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N/A
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Countries of recruitment
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Switzerland
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Contacts
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Name:
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Susi
Saxer |
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Address:
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Rosenbergstrasse 59
9001
St.Gallen
Switzerland |
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Telephone:
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+41 71 226 15 20 |
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Email:
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susi.saxer@fhsg.ch |
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Affiliation:
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Fachhochschule St.Gallen / Institut für Angewandte Pflegewissenschaft |
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Name:
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Susi
Saxer |
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Address:
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Rosenbergstrasse 59
9001
St.Gallen
Switzerland |
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Telephone:
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+41 71 226 15 20 |
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Email:
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susi.saxer@fhsg.ch |
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Affiliation:
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Fachhochschule St.Gallen / Institut für Angewandte Pflegewissenschaft |
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Key inclusion & exclusion criteria
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Inclusion criteria: -Parkinson's disease
-Urinary incontinence
-living at home or in a nursing home after discharge
-german speaking
Exclusion criteria: -Urinary catheter
- MMST<18
-Depression
-Delir, Hallucinations
-living in a nursing home
Age minimum:
18 Years
Age maximum:
None
Gender:
All
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Health Condition(s) or Problem(s) studied
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G20
R32
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Parkinson disease
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Unspecified urinary incontinence
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Intervention(s)
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Group 1: Contol-group: usual care (Duration: during the whole stay in the rehabilitation clinic (normally 3 weeks) and support at home up to eight week after discharge)
Group 2: Interventiongroup: The intervention is carried out by nurses in collaboration with the patients and includes four steps: Assessment of urinary incontinence, care planning, individual interventions and discharge management with supervision at home (Duration: during the whole stay in the rehabilitation clinic (normally 3 weeks) and support at home up to eight week after discharge).
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Primary Outcome(s)
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Incontinence (pad-test, micturition diary, ICIQ-SF questionnaire, 3 months after discharge)
Quality of life (I-QOL questionnaire, 3 months after discharge)
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Secondary Outcome(s)
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Nurses:
Knowledge about urinary incontinence and their workload
Time of measurement: three points of measurement; at the beginning of the control phase, between the control and intervention phase (before the education of the intervention), at the end of the intervention phase
Questionnaire: self-developed questionnaire about knowledge of incontinence, Short Questionnaire for work analysis
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Source(s) of Monetary Support
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Ebnet Stiftung
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Ethics review
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Status: Approved
Approval date: 16/03/2015
Contact:
Kantonale Ethikkommission Thurgau
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