Multicenter Implementation of E-monitoring in Parkinson's Disease (EPD)
Primary Purpose
Parkinson Disease
Status
Active
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Sanacoach Parkinson (SCP)
Sponsored by
About this trial
This is an interventional other trial for Parkinson Disease focused on measuring Parkinson's Disease, Telemonitoring, Cost effectiveness, Quality of care, eHealth
Eligibility Criteria
Inclusion Criteria:
- Diagnosis according to the Movement Disorder Society Clinical Diagnostic Criteria for Parkinson's Disease
- Disease duration ≥ 3 months.
- Able to complete the questionnaires and use the Sanacoach Parkinson, independently or with the help of an informal caregiver.
Exclusion Criteria:
- Not able to understand and/or sign the informed consent.
- No access to the internet via computer, tablet or smartphone.
- Participating in other trial
Sites / Locations
- Meander Medical Center
- Onze Lieve Vrouwe Hospital
- Rode Kruis Hospital
- Zuyderland Medical Center
- Zuyderland Medical Center
- Elkerliek Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Participants
Arm Description
Intervention: use of SCP
Outcomes
Primary Outcome Measures
Patient-experienced quality of care
Measured by the net-promoter score. Each patient rates their care received on a scale of 0 to 10. Detractors (scoring 0-6) are subtracted from promoters (scoring 9-10), leaving the net-promoter score. The score ranges from -100 to +100, with higher scores indicating better patient-experienced quality of care.
Patient-satisfaction with the Sanacoach Parkinson
Measured by an 11-item patient satisfaction questionnaire. Score range = 1-45, with higher scores indicating better patient satisfaction.
Disease-related quality of life
Measured by the 8-item Parkinson's disease questionnaire (PDQ-8), range 0-32, higher scores indicate worse quality of life
Disease-related health care costs
Calculated by measuring the number of PD-relates visits, telephone contacts and e-mail contacts with a neurologist, specialized nurse or general practitioner; number of hospitalizations, hospitalization days and emergency room visits related to PD, head trauma, hip fracture, pneumonia or psychosis; number of visits to a physiotherapist, occupational therapist, speech therapist or psychologist; number of days receiving inpatient of outpatient care at a rehabilitation center or nursing home; hours of formal and informal care received, days of labor missed and time spent by neurologists and specialized nurses on monitoring the Sanacoach Parkinson and follow-up activities. All these variables will be converted to costs per year (in euros).
Secondary Outcome Measures
Patient self-management
Measured by the Partners In Health scale, range 0-96, higher scores indicate better self-management
Caregiver burden
Measured by the Caregiver Strain Index, range 0-13, higher scores indicate higher caregiver burden
Disease-severity
Measured by the Unified Parkinson's Disease Rating Scale (UPDRS), range 0-260, higher scores indicate increased disease-severity
Healthcare professional's attitude towards the Sanacoach Parkinson
Measured by a 9-item questionnaire, range 0-36, higher scores indicate better satisfaction with the Sanacoach Parkinson
Full Information
NCT ID
NCT05164783
First Posted
October 28, 2021
Last Updated
July 24, 2023
Sponsor
Zuyderland Medisch Centrum
Collaborators
AbbVie
1. Study Identification
Unique Protocol Identification Number
NCT05164783
Brief Title
Multicenter Implementation of E-monitoring in Parkinson's Disease
Acronym
EPD
Official Title
Multicenter Implementation of E-monitoring in Parkinson's Disease
Study Type
Interventional
2. Study Status
Record Verification Date
July 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
November 23, 2021 (Actual)
Primary Completion Date
April 2025 (Anticipated)
Study Completion Date
April 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Zuyderland Medisch Centrum
Collaborators
AbbVie
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
Introduction and rationale:
Parkinson´s disease (PD) is a slowly progressive and chronic disease, characterized by a range of motor and non-motor symptoms such as bradykinesia, tremor and falls, but also sleep disturbance, cognitive decline, behavioral problems and autonomic failure. These symptoms often fluctuate over time and between patients. These fluctuating and often debilitating symptoms necessitate proper monitoring. Due to this complexity, most patients require long-term specialized care. The current prevalence of PD in the Netherlands is estimated at 600-775 per 100.000 persons. This figure is expected to increase with > 50% in 2040. Combined with rising healthcare costs and a projected reduction in the number of available healthcare professionals, a system of frequent outpatient visits with a movement disorder specialist, as is currently the standard of care for PD in most (Dutch) hospitals, will likely not be sustainable.
Additionally, improvements can be made in the quality of care for PD-patients. The most important aspect mentioned by patients is improved self-management. Other points of improvement are: communication between different healthcare professionals involved; advanced care planning and having a single point of access / personal case manager. Recently an international group of experts in the field of PD have published a viewpoint article concerning their ideas for the optimization of the care for PD-patients. In addition to the previous points, these experts mention: providing care at home rather than in hospital; pro-active instead of reactive care and improvement of the expertise of healthcare professionals.
A possible solution to improving the sustainability of care for PD-patients, and addressing several of the issues concerning quality of care, lies in the use of telemedicine (or eHealth): the remote diagnosis and treatment of patients by means of telecommunications technology. Telemedicine exists in a wide variety of forms, one of which is 'telemonitoring'; the home monitoring of patients. In 2017 it was shown that telemonitoring is save and led to a significant reduction in health care consumption in patients with inflammatory bowel disease. Furthermore, studies in several chronic diseases have shown that telemonitoring leads to better patient empowerment and improved self-management. Self-management is in itself associated with improved health status and well-being in patients with a chronic disease as well as with a reduction in healthcare consumption.
In collaboration with Sananet, Zuyderland Medical Center has developed a telemonitoring tool for PD called 'SanaCoach Parkinson' (SCP). It is, to the investigators knowledge, the first telemonitoring tool for PD that uses anamnestic data from targeted questionnaires to monitor patients with PD. Trough the SCP both motor and non-motor aspects of PD are screened pro-actively. It allows patients to remain at home rather that visit the outpatient clinic. Additionally, proactive monitoring of symptoms leads to earlier detection of deterioration. This gives the neurologist the possibility to optimize (medical) treatment before further, costly, complications arise. Furthermore, the SCP improves patients' insight in their disease, supporting self-management.
A previous pilot-study into the effect of implementation of this tool showed that the use of the SCP was feasible in an outpatient care setting and that patient satisfaction and experienced quality of care were high. Additionally, the use of the SCP led to a significant reduction in the number of outpatient visits as well as the PD-related healthcare costs in Zuyderland Medical Center in the first year of use of the SCP.
Hypotheses:
The investigators hypothesize that implementation of telemonitoring via the SCP will be non-inferior to treatment as usual (TAU) with regards to the quality of care as experienced by PD-patients, while reducing the PD-related healthcare consumption and costs.
Secondly the investigators hypothesize that telemonitoring via the SCP will improve the quality of care for PD-patients compared to TAU.
Study Design and procedures:
This will be a non-randomized, prospective, multi-center, non-inferiority, implementation study. During 1 year, all consecutive PD-patients in the neurology outpatient clinic of each participating hospital that meet the in- and exclusion criteria will be invited to join this study. Participants will be monitored via the SCP for 2 years. During this time, PD-related outpatient visits with either a neurologist of specialized nurse will be set at 1-2 per patient per year, with a maximum total planned duration of 60 minutes. If this is not feasible, the primary reason for this will be recorded.
New hospitals may join the study until 6 months after the inclusion of the first patient.
Assessments will take place at baseline, 1 year and 2 years.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parkinson Disease
Keywords
Parkinson's Disease, Telemonitoring, Cost effectiveness, Quality of care, eHealth
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Implementation study with stepwise approach
Masking
None (Open Label)
Allocation
N/A
Enrollment
258 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Participants
Arm Type
Experimental
Arm Description
Intervention: use of SCP
Intervention Type
Combination Product
Intervention Name(s)
Sanacoach Parkinson (SCP)
Intervention Description
A web-based monitoring tool for patients with PD, using questionnaires. It includes nine parts: 1) A 89-question, quarterly questionnaire about PD-symptoms. 2) Questionnaire responses are converted to scores on 16 PD-related domains. Both the current score and the score's change compared to the previous questionnaire are visible. 3) An interim evaluation is sent after 6 weeks with questions on any domains where a patient indicated problems. 4) A medication monitor can be initialized by the treating physician to evaluate the effect of a therapeutic change. 5) A consultation preparation module allows patients to indicate which topics they want to discuss during an outpatient visit. 6) Patients can ask for 'calling advise' if they are unsure whether to contact their physician. 7) Patients and healthcare providers can send each other text messages. 8) Interactive learning modules about PD. 9) Annual evaluation regarding patient satisfaction, self-management and healthcare consumption.
Primary Outcome Measure Information:
Title
Patient-experienced quality of care
Description
Measured by the net-promoter score. Each patient rates their care received on a scale of 0 to 10. Detractors (scoring 0-6) are subtracted from promoters (scoring 9-10), leaving the net-promoter score. The score ranges from -100 to +100, with higher scores indicating better patient-experienced quality of care.
Time Frame
Change between baseline and after two years of using the Sanacoach Parkinson
Title
Patient-satisfaction with the Sanacoach Parkinson
Description
Measured by an 11-item patient satisfaction questionnaire. Score range = 1-45, with higher scores indicating better patient satisfaction.
Time Frame
Measured after 2 years of using the Sanacoach Parkinson
Title
Disease-related quality of life
Description
Measured by the 8-item Parkinson's disease questionnaire (PDQ-8), range 0-32, higher scores indicate worse quality of life
Time Frame
Change between baseline and after two years of using the Sanacoach Parkinson
Title
Disease-related health care costs
Description
Calculated by measuring the number of PD-relates visits, telephone contacts and e-mail contacts with a neurologist, specialized nurse or general practitioner; number of hospitalizations, hospitalization days and emergency room visits related to PD, head trauma, hip fracture, pneumonia or psychosis; number of visits to a physiotherapist, occupational therapist, speech therapist or psychologist; number of days receiving inpatient of outpatient care at a rehabilitation center or nursing home; hours of formal and informal care received, days of labor missed and time spent by neurologists and specialized nurses on monitoring the Sanacoach Parkinson and follow-up activities. All these variables will be converted to costs per year (in euros).
Time Frame
Change of average costs per year during the two years of using the Sanacoach Parkinson, compared to a 6 month period before use of the Sanacoach Parkinson
Secondary Outcome Measure Information:
Title
Patient self-management
Description
Measured by the Partners In Health scale, range 0-96, higher scores indicate better self-management
Time Frame
Change between baseline and after two years of using the Sanacoach Parkinson
Title
Caregiver burden
Description
Measured by the Caregiver Strain Index, range 0-13, higher scores indicate higher caregiver burden
Time Frame
Change between baseline and after two years of using the Sanacoach Parkinson
Title
Disease-severity
Description
Measured by the Unified Parkinson's Disease Rating Scale (UPDRS), range 0-260, higher scores indicate increased disease-severity
Time Frame
Change between baseline and after two years of using the Sanacoach Parkinson
Title
Healthcare professional's attitude towards the Sanacoach Parkinson
Description
Measured by a 9-item questionnaire, range 0-36, higher scores indicate better satisfaction with the Sanacoach Parkinson
Time Frame
Measured 6-monthly during 3 years of working with the Sanacoach Parkinson
Other Pre-specified Outcome Measures:
Title
Compliance with Sanacoach Parkinson
Description
Number of periodic questionnaires completed, patients completing <3 questionnaires a year are defined as non-compliant
Time Frame
During the 2 years of using the Sanacoach Parkinson
Title
Number of patients requiring additional outpatient visits
Description
% of patient years in which a patient requires more than 2 outpatient visits
Time Frame
During the 2 years of using the Sanacoach Parkinson
Title
Reasons for additional outpatient visits
Description
Descriptive summary of the reasons patient required additional outpatient visits, as specified by healthcare providers. Pre-specified options are: 1) Doctor-initiated, physical examination needed 2) Doctor-initiated, deepen history 3) Doctor-initiated, nature of problem 4) Patient-initiated and 5) Caregiver-initiated
Time Frame
During the 2 years of using the Sanacoach Parkinson
10. Eligibility
Sex
All
Minimum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosis according to the Movement Disorder Society Clinical Diagnostic Criteria for Parkinson's Disease
Disease duration ≥ 3 months.
Able to complete the questionnaires and use the Sanacoach Parkinson, independently or with the help of an informal caregiver.
Exclusion Criteria:
Not able to understand and/or sign the informed consent.
No access to the internet via computer, tablet or smartphone.
Participating in other trial
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gerrit Tissingh, MD, PhD
Organizational Affiliation
Zuyderland MC
Official's Role
Principal Investigator
Facility Information:
Facility Name
Meander Medical Center
City
Amersfoort
Country
Netherlands
Facility Name
Onze Lieve Vrouwe Hospital
City
Amsterdam
Country
Netherlands
Facility Name
Rode Kruis Hospital
City
Beverwijk
Country
Netherlands
Facility Name
Zuyderland Medical Center
City
Geleen
Country
Netherlands
Facility Name
Zuyderland Medical Center
City
Heerlen
Country
Netherlands
Facility Name
Elkerliek Hospital
City
Helmond
Country
Netherlands
12. IPD Sharing Statement
Plan to Share IPD
No
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Links:
URL
https://www.volksgezondheidenzorg.info/onderwerp/ziekte-van-parkinson/cijfers-context/huidige-situatie
Description
Information on the epidemiology of Parkinson's Disease in the Netherlands, from the 'Rijksinstituut voor Volksgezondheid en Milieu' (RIVM), the Dutch National Institute for Health and Environment
URL
https://www.pbl.nl/sites/default/files/downloads/PBL_2013_Demografische_ontwikkelingen-2010-2040_1044.pdf
Description
Report on demographic changes in the Netherlands from 2010 to 2040, by the 'Planbureau voor de Leefomgeving', the Dutch national institute for strategic policy analysis in the field of environment, nature and space
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Multicenter Implementation of E-monitoring in Parkinson's Disease
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