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Cognitive Therapy for Urinary Dysfunction in Parkinson´s Disease (PD-UD)

Primary Purpose

Parkinson Disease, Urinary Disease Other

Status
Unknown status
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
cognitive training
pelvic floor training
Sponsored by
University Hospital Schleswig-Holstein
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Parkinson Disease

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • consenting capacity (MOCA >17) and written consent
  • idiopathic parkinson syndrome according to UK Brain Bank criteria
  • female gender

Exclusion Criteria:

  • missing consenting capacity (MOCA <18)
  • current depressive episode (BDI > 18)
  • current intake of medication for the treatment of bladder dysfunction

Sites / Locations

  • Department of Neurology, University Hospital Schleswig-HolsteinRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

cognitive training

pelvic floor training

Arm Description

The cognitive training the investigators are planning consists of three modules which, in their entirety, are intended to help improve bladder dysfunction, which leads to psychological distress in patients: psychoeducation, training of cognitive functions and training in behavioural therapeutic techniques. The training will take place over six weeks, with two sessions per week in the first three weeks. In the following three weeks the frequency will be reduced to once a week so that there will be 9 sessions. The duration of each training session is 90 minutes.

At the beginning of the training, perception of the pelvic floor is the most important factor. The patients should learn the motor skills to consciously perceive and feel the pelvic floor muscles. This requires a lot of concentration and movement control. After this perception phase, the learned movements are internalized. The fine coordination of the pelvic floor muscles is more harmonious and the tensing and relaxing of the muscles becomes easier over time. In the last phase of the training, the movements and muscle activations should be internalised in such a way that they are anchored as automated movement patterns. The training will take place over six weeks, with two sessions per week in the first three weeks. In the following three weeks the frequency will be reduced to once a week so that there will be 9 sessions. The duration of each training session is 90 minutes.

Outcomes

Primary Outcome Measures

Change in the International Consultation on Incontinence Questionnaire Overactive Bladder Module (ICIQ-OAB)
The ICIQ-OAB is a questionnaire for evaluating overactive bladder and related impact on quality of life (QoL) and outcome of treatment in men and women in research and clinical practice across the world. The ICIQ-OAB is derived from the fully validated ICSmale and BFLUTS questionnaires and provides a measure to assess the impact of urinary frequency, urgency, urge incontinence and nocturia symptoms.
Change in the International Consultation on Incontinence Questionnaire Lower Urinary Tract Symptoms Quality of Life Module (ICIQ-LUTSqol)
The ICIQ-LUTSqol is a psychometrically robust patient-completed questionnaire evaluating quality of life (QoL) in urinary incontinent patients for use in research and clinical practice across the world. The ICIQ-LUTSqol is the King's Health Questionnaire (KHQ) adapted for use within the ICIQ structure and provides a measure to assess the impact of urinary incontinence on quality of life with particular reference to social effects. It is an ideal research tool as it explores in detail the impact on patients' lives of urinary incontinence and can be used as an outcome measure to assess impact of different treatment modalities.
Change in the Patient Perception of Bladder Condition (PPBC)
The PPBC is a single-item, global outcome measure for urinary incontinence.
Change in the International Prostate Symptom Score (I-PSS)
The International Prostate Symptom Score (I-PSS) is based on the answers to seven questions concerning urinary symptoms and one question concerning quality of life. Each question concerning urinary symptoms allows the patient to choose one out of six answers indicating increasing severity of the particular symptom. The answers are assigned points from 0 to 5. The total score can therefore range from 0 to 35 (asymptomatic to very symptomatic).
Change in the Uroflowmetric
Uroflowmetry measures the flow of urine. It tracks how fast urine flows, how much flows out, and how long it takes. It's a diagnostic test to assess how well the urinary tract functions.

Secondary Outcome Measures

Change in the Verbal memory function through the Rey Auditory Verbal Learning Test (RAVLT)
Participants are given a list of 15 unrelated words repeated over five different trials and are asked to repeat. Another list of 15 unrelated words are given and the client must again repeat the original list of 15 words and then again after 30 minutes.
Change in the Visuomotor abilities and nonverbal memory Rey-Osterrieth complex figure test (ROCF)
The Rey-Osterrieth complex figure test (ROCF) is a neuropsychological assessment in which patients are asked to reproduce a complicated line drawing, first by copying it freehand (recognition; measures visuomotor abilities), and then drawing from memory (recall; measures nonverbal memory).
Change in the Verbal short term memory functions through the Digit Span test
Verbal short term memory span measures the number of discrete units over which the patient can successively distribute his attention and still organize them into a working unit. To generalize, it refers to the ability of the patient to reproduce immediately, after one presentation, a series of discrete stimuli in their original order.
Change in the Response inhibition through the Stroop test
The Stroop test is a widely used measure of selective attention that requires interference resolution, response inhibition, and response selection.
Change in the Visual attention and task switching though the Trial Making Test
The Trail Making Test is a neuropsychological test of visual attention and task switching. It consists of two parts in which the subject is instructed to connect a set of 25 dots as quickly as possible while still maintaining accuracy.
Change in the Word fluency through the Regensburger Word Fluency Test
In the Regensburger Word Fluency Test patients have to produce as many words as possible from a given category or beginning with a specific letter within 2 minutes.

Full Information

First Posted
April 1, 2019
Last Updated
April 12, 2019
Sponsor
University Hospital Schleswig-Holstein
Collaborators
University of Kiel
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1. Study Identification

Unique Protocol Identification Number
NCT03917732
Brief Title
Cognitive Therapy for Urinary Dysfunction in Parkinson´s Disease
Acronym
PD-UD
Official Title
Randomized Controlled Study to Evaluate the Efficacy of a Cognitive Training Approach to Improve Urinary Dysfunction in Parkinson's Disease
Study Type
Interventional

2. Study Status

Record Verification Date
April 2019
Overall Recruitment Status
Unknown status
Study Start Date
April 2019 (Anticipated)
Primary Completion Date
September 2019 (Anticipated)
Study Completion Date
December 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital Schleswig-Holstein
Collaborators
University of Kiel

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Idiopathic Parkinson's syndrome (IPS) is one of the most common neurodegenerative diseases. The prevalence and significance of this disease is continuously increasing in the course of demographic change. For many decades, the focus of diagnostics and therapy was on the motor symptoms of IPS. Only in recent years, it has been recognized that Parkinson's patients also suffer from a variety of non-motor symptoms. These have a decisive influence on the patient's quality of life. As one of the most common non-motor symptoms, 55 to 80% of IPS patients suffer from urinary dysfunction. This is associated with a very high impairment of quality of life due to a high degree of stigmatization and impairment of social participation. In clinical everyday life, Parkinson's patients regularly report the occurrence of a strong imperative urge to urinate, which occurs suddenly and is usually triggered by a certain external stimuli. Specific cognitive processing and reflection of these external stimuli seems to help overcome the imperative urge to urinate. From this clinical observation, it can be assumed that the imperative urge to urinate is subject to a certain cognitive control in the sense of targeted inhibition. The pharmacological therapy of urinary dysfunction in IPS patients is severely restricted and characterized by insufficient proof of efficacy as well as a high potential for side effects. In clinical practice, alpha-blockers and anticholinergics are frequently used, but the evidence base for IPS is inadequate. In addition, there is a highly relevant risk for Parkinson's patients of specific side effects such as orthostatic dysregulation or deterioration of cognition up to psychoses and hallucinations. This greatly limits their use especially in older IPS patients. While the use of dopaminergic medication is essential for the treatment of motor symptoms in Parkinson's patients, a large number of studies have not confirmed sufficient evidence for the efficacy of dopaminergic medication in urinary dysfunction. In addition, non-pharmacological therapy options, in particular pelvic floor training, are used to treat bladder dysfunction. Due to the lack of risk of side effects, pelvic floor training is currently recommended as a first-line therapy option for IPS patients. Initial studies have shown positive effects, but due to the lack of randomized controlled trials, a sufficient evidence base for this has not yet been established. The aim of the study is to examine whether a purely cognitive therapy approach is suitable to improve subjective and objective symptoms of urinary dysfunction in IPS patients. This therapeutic approach will be compared with the gold standard of pelvic floor training in terms of efficacy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parkinson Disease, Urinary Disease Other

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
45 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
cognitive training
Arm Type
Experimental
Arm Description
The cognitive training the investigators are planning consists of three modules which, in their entirety, are intended to help improve bladder dysfunction, which leads to psychological distress in patients: psychoeducation, training of cognitive functions and training in behavioural therapeutic techniques. The training will take place over six weeks, with two sessions per week in the first three weeks. In the following three weeks the frequency will be reduced to once a week so that there will be 9 sessions. The duration of each training session is 90 minutes.
Arm Title
pelvic floor training
Arm Type
Active Comparator
Arm Description
At the beginning of the training, perception of the pelvic floor is the most important factor. The patients should learn the motor skills to consciously perceive and feel the pelvic floor muscles. This requires a lot of concentration and movement control. After this perception phase, the learned movements are internalized. The fine coordination of the pelvic floor muscles is more harmonious and the tensing and relaxing of the muscles becomes easier over time. In the last phase of the training, the movements and muscle activations should be internalised in such a way that they are anchored as automated movement patterns. The training will take place over six weeks, with two sessions per week in the first three weeks. In the following three weeks the frequency will be reduced to once a week so that there will be 9 sessions. The duration of each training session is 90 minutes.
Intervention Type
Behavioral
Intervention Name(s)
cognitive training
Intervention Description
The cognitive training the investigators are planning consists of three modules which, in their entirety, are intended to help improve bladder dysfunction, which leads to psychological distress in patients: psychoeducation, training of cognitive functions and training in behavioural therapeutic techniques. The training will take place over six weeks, with two sessions per week in the first three weeks. In the following three weeks the frequency will be reduced to once a week so that there will be 9 sessions. The duration of each training session is 90 minutes.
Intervention Type
Behavioral
Intervention Name(s)
pelvic floor training
Intervention Description
At the beginning of the training, perception of the pelvic floor is the most important factor. The patients should learn the motor skills to consciously perceive and feel the pelvic floor muscles. This requires a lot of concentration and movement control. After this perception phase, the learned movements are internalized. The fine coordination of the pelvic floor muscles is more harmonious and the tensing and relaxing of the muscles becomes easier over time. In the last phase of the training, the movements and muscle activations should be internalised in such a way that they are anchored as automated movement patterns. The training will take place over six weeks, with two sessions per week in the first three weeks. In the following three weeks the frequency will be reduced to once a week so that there will be 9 sessions. The duration of each training session is 90 minutes.
Primary Outcome Measure Information:
Title
Change in the International Consultation on Incontinence Questionnaire Overactive Bladder Module (ICIQ-OAB)
Description
The ICIQ-OAB is a questionnaire for evaluating overactive bladder and related impact on quality of life (QoL) and outcome of treatment in men and women in research and clinical practice across the world. The ICIQ-OAB is derived from the fully validated ICSmale and BFLUTS questionnaires and provides a measure to assess the impact of urinary frequency, urgency, urge incontinence and nocturia symptoms.
Time Frame
4 weeks before beginning and 4 weeks after completion of the training
Title
Change in the International Consultation on Incontinence Questionnaire Lower Urinary Tract Symptoms Quality of Life Module (ICIQ-LUTSqol)
Description
The ICIQ-LUTSqol is a psychometrically robust patient-completed questionnaire evaluating quality of life (QoL) in urinary incontinent patients for use in research and clinical practice across the world. The ICIQ-LUTSqol is the King's Health Questionnaire (KHQ) adapted for use within the ICIQ structure and provides a measure to assess the impact of urinary incontinence on quality of life with particular reference to social effects. It is an ideal research tool as it explores in detail the impact on patients' lives of urinary incontinence and can be used as an outcome measure to assess impact of different treatment modalities.
Time Frame
4 weeks before beginning and 4 weeks after completion of the training
Title
Change in the Patient Perception of Bladder Condition (PPBC)
Description
The PPBC is a single-item, global outcome measure for urinary incontinence.
Time Frame
4 weeks before beginning and 4 weeks after completion of the training
Title
Change in the International Prostate Symptom Score (I-PSS)
Description
The International Prostate Symptom Score (I-PSS) is based on the answers to seven questions concerning urinary symptoms and one question concerning quality of life. Each question concerning urinary symptoms allows the patient to choose one out of six answers indicating increasing severity of the particular symptom. The answers are assigned points from 0 to 5. The total score can therefore range from 0 to 35 (asymptomatic to very symptomatic).
Time Frame
4 weeks before beginning and 4 weeks after completion of the training
Title
Change in the Uroflowmetric
Description
Uroflowmetry measures the flow of urine. It tracks how fast urine flows, how much flows out, and how long it takes. It's a diagnostic test to assess how well the urinary tract functions.
Time Frame
4 weeks before beginning and 4 weeks after completion of the training
Secondary Outcome Measure Information:
Title
Change in the Verbal memory function through the Rey Auditory Verbal Learning Test (RAVLT)
Description
Participants are given a list of 15 unrelated words repeated over five different trials and are asked to repeat. Another list of 15 unrelated words are given and the client must again repeat the original list of 15 words and then again after 30 minutes.
Time Frame
4 weeks before beginning and 4 weeks after completion of the training
Title
Change in the Visuomotor abilities and nonverbal memory Rey-Osterrieth complex figure test (ROCF)
Description
The Rey-Osterrieth complex figure test (ROCF) is a neuropsychological assessment in which patients are asked to reproduce a complicated line drawing, first by copying it freehand (recognition; measures visuomotor abilities), and then drawing from memory (recall; measures nonverbal memory).
Time Frame
4 weeks before beginning and 4 weeks after completion of the training
Title
Change in the Verbal short term memory functions through the Digit Span test
Description
Verbal short term memory span measures the number of discrete units over which the patient can successively distribute his attention and still organize them into a working unit. To generalize, it refers to the ability of the patient to reproduce immediately, after one presentation, a series of discrete stimuli in their original order.
Time Frame
4 weeks before beginning and 4 weeks after completion of the training
Title
Change in the Response inhibition through the Stroop test
Description
The Stroop test is a widely used measure of selective attention that requires interference resolution, response inhibition, and response selection.
Time Frame
4 weeks before beginning and 4 weeks after completion of the training
Title
Change in the Visual attention and task switching though the Trial Making Test
Description
The Trail Making Test is a neuropsychological test of visual attention and task switching. It consists of two parts in which the subject is instructed to connect a set of 25 dots as quickly as possible while still maintaining accuracy.
Time Frame
4 weeks before beginning and 4 weeks after completion of the training
Title
Change in the Word fluency through the Regensburger Word Fluency Test
Description
In the Regensburger Word Fluency Test patients have to produce as many words as possible from a given category or beginning with a specific letter within 2 minutes.
Time Frame
4 weeks before beginning and 4 weeks after completion of the training
Other Pre-specified Outcome Measures:
Title
Changes in functional magnet resonance imaging (fMRI) within a Go/NoGo paradigm
Description
The investigators aim to answer the question whether there are different activity patterns in Parkinson's patients with bladder dysfunction compared to Parkinson's patients without bladder dysfunction in the areas involved in bladder function regulation while concerning a Go/NoGo paradigm.
Time Frame
4 weeks before beginning and 4 weeks after completion of the training

10. Eligibility

Sex
Female
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: consenting capacity (MOCA >17) and written consent idiopathic parkinson syndrome according to UK Brain Bank criteria female gender Exclusion Criteria: missing consenting capacity (MOCA <18) current depressive episode (BDI > 18) current intake of medication for the treatment of bladder dysfunction
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Inken Rothkirch, Dr. phil.
Phone
0431 500 23985
Email
i.rothkirch@neurologie.uni-kiel.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Daniela Berg, Prof. Dr.
Organizational Affiliation
Department of Neurology, University Hospital Schleswig- Holstein
Official's Role
Study Director
Facility Information:
Facility Name
Department of Neurology, University Hospital Schleswig-Holstein
City
Kiel
State/Province
Schleswig-Holstein
ZIP/Postal Code
24105
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Inken Rothkirch, Dr. phil.
Phone
0431 500 23985
Email
i.rothkirch@neurologie.uni-kiel.de
First Name & Middle Initial & Last Name & Degree
Inken Rothkirch, Dr. phil.
First Name & Middle Initial & Last Name & Degree
Eva Schaeffer, Dr. med.

12. IPD Sharing Statement

Learn more about this trial

Cognitive Therapy for Urinary Dysfunction in Parkinson´s Disease

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