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Digitised Home Based Care for Parkinson's Disease

Primary Purpose

Parkinson Disease, Parkinson

Status
Not yet recruiting
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Digital Home Based Care pathway
Sponsored by
University of Plymouth
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Parkinson Disease focused on measuring Parkinson Disease, Self-Management, Telemedicine, Artificial Intelligence

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18 years or over
  • Not resident in care home or nursing home
  • Ambulant
  • Have compatible smartphone/data access (access to a digital device is a necessary prerequisite of system use, and the formative usability study had success in recruiting participants with varying levels of experience with smartphones [18])
  • Be fluent in English
  • Normally under the care of the Parkinson's service in the participating organisation
  • Participant's healthcare provider in the participating organisation consented to participate in the study
  • Able and willing to provide informed consent
  • Able and willing to comply with intervention requirements

Exclusion Criteria:

  • Secondary cause of parkinsonism
  • Significant cognitive impairment or a diagnosis of Parkinson's disease dementia
  • Significant comorbidity, which in the opinion of the chief investigator would preclude safe participation in the study or protocol compliance
  • Previous involvement in development or testing of the NMS Assist system
  • A life expectancy of <6 months
  • Living in residential care facilities
  • Incapable of self-consent
  • In a dependent/unequal relationship with the research or care teams or any PPI representatives

Sites / Locations

  • University of Plymouth

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Digitised Home Based Care pathway

Arm Description

The investigators have co-designed an innovative digital care pathway, Home Based Care (HBC), that delivers self-management support and clinical expertise to the patient's home, supported by digitally-enabled remote monitoring with a wrist-worn sensor, the Parkinson's Kinetograph, and digitally-delivered questionnaires, to replace the current pen-and-paper processes.

Outcomes

Primary Outcome Measures

Uptake
Rates of conversion to the digital platform
Degree of compliance with wearable sensor
The wearable sensors are worn on the wrist and are known as the Parkinson's Kinetograph (PKG). The PKG assess objective motor measures including bradykinesia, dyskinesia and tremor. In accordance with the HBC pathway, patients are required to wear the PKG for 6 days and nights, after which the results are analyzed by their care team. From these results, therefore, it is clear to see where the patient has complied with wearing the PKG for the allotted time frame.
Proportion of digital questionnaires completed
In accordance with HBC pathway, patients are required to complete a set of questionnaires covering the same time period in which they are wearing the PKG, and are responsible for assessing subjective measures. This outcome will assess compliance by examining the patients' overall compliance with the digital monitoring questionnaires by calculating how many of the questionnaires they successfully complete over the study period.
Engagement
Qualitative feedback about engagement from semi-structured interviews

Secondary Outcome Measures

Usability scores
System Usability Scale, 5-point Likert scale with total scores ranging from 0-100
Patient perceptions of usability
Qualitative feedback about usability from semi-structured interviews
Patient perceptions of acceptability
Qualitative feedback about acceptability from semi-structured interviews
Cost impact
Preliminary evaluation of implementation costs; costs required to implement the digital HBC pathway will be compared to the costs of delivering the standard care pathway

Full Information

First Posted
September 1, 2022
Last Updated
May 10, 2023
Sponsor
University of Plymouth
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1. Study Identification

Unique Protocol Identification Number
NCT05544305
Brief Title
Digitised Home Based Care for Parkinson's Disease
Official Title
Digitised Home Based Care for Parkinson's Disease
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
January 1, 2024 (Anticipated)
Primary Completion Date
June 1, 2025 (Anticipated)
Study Completion Date
June 1, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Plymouth

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
Parkinson's disease is the world's fastest-growing neurological condition. It is a progressive neurodegenerative disorder that causes a wide range of movement-related (motor) problems (slowness, stiffness, tremor, balance difficulties) and non-motor problems (disturbances of thinking, memory, perception, mood, bladder, bowels, blood pressure). Even before the pandemic, NHS services were struggling to meet the demand for care. To address this need for support, the investigators have co-designed an innovative digital care pathway, Home Based Care (HBC), with people with Parkinson's (PwP) and care partners (CP) to deliver self-management support and clinical expertise to the patient's home. This pathway is supported by remote monitoring with a wrist-worn sensor and questionnaires. In this study, the investigators will be digitising this pathway so that data from a variety of sources (including the sensor, questionnaires, and patients' health records) can be combined in one place to enable more personalised care and to provide advice to support self-management of symptoms by patients. After the investigators have set up the digitised pathway, its implementation will be evaluated with a group of 120 people with Parkinson's and their care partners and associated healthcare providers through the Plymouth Parkinson's Service. The investigators will examine participants' adoption of and engagement with the patient-facing digital platform over the course of 3 months and gather their feedback about its usability and acceptability. A smaller group of the participants will discuss their experiences in more detail to help pinpoint aspects that work well and those needing adjustment and development. The investigators anticipate that this system will result in improved quality of life and care and increased knowledge and confidence for self-managing symptoms. The results of the study will be used to improve the digitised Home Based Care pathway. People with Parkinson's and care partners involved in the project will help guide the sharing of these results with healthcare providers and the general public.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parkinson Disease, Parkinson
Keywords
Parkinson Disease, Self-Management, Telemedicine, Artificial Intelligence

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Masking Description
No blinding will be possible in the study.
Allocation
N/A
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Digitised Home Based Care pathway
Arm Type
Experimental
Arm Description
The investigators have co-designed an innovative digital care pathway, Home Based Care (HBC), that delivers self-management support and clinical expertise to the patient's home, supported by digitally-enabled remote monitoring with a wrist-worn sensor, the Parkinson's Kinetograph, and digitally-delivered questionnaires, to replace the current pen-and-paper processes.
Intervention Type
Other
Intervention Name(s)
Digital Home Based Care pathway
Intervention Description
The digital version of the pathway includes an integrated data platform with an automated patient flow management system, digitised patient-reported outcome on web-based patient portal, and AI-based automated reporting for clinical decision support.
Primary Outcome Measure Information:
Title
Uptake
Description
Rates of conversion to the digital platform
Time Frame
3 months
Title
Degree of compliance with wearable sensor
Description
The wearable sensors are worn on the wrist and are known as the Parkinson's Kinetograph (PKG). The PKG assess objective motor measures including bradykinesia, dyskinesia and tremor. In accordance with the HBC pathway, patients are required to wear the PKG for 6 days and nights, after which the results are analyzed by their care team. From these results, therefore, it is clear to see where the patient has complied with wearing the PKG for the allotted time frame.
Time Frame
3 months
Title
Proportion of digital questionnaires completed
Description
In accordance with HBC pathway, patients are required to complete a set of questionnaires covering the same time period in which they are wearing the PKG, and are responsible for assessing subjective measures. This outcome will assess compliance by examining the patients' overall compliance with the digital monitoring questionnaires by calculating how many of the questionnaires they successfully complete over the study period.
Time Frame
3 months
Title
Engagement
Description
Qualitative feedback about engagement from semi-structured interviews
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Usability scores
Description
System Usability Scale, 5-point Likert scale with total scores ranging from 0-100
Time Frame
3 months
Title
Patient perceptions of usability
Description
Qualitative feedback about usability from semi-structured interviews
Time Frame
3 months
Title
Patient perceptions of acceptability
Description
Qualitative feedback about acceptability from semi-structured interviews
Time Frame
3 months
Title
Cost impact
Description
Preliminary evaluation of implementation costs; costs required to implement the digital HBC pathway will be compared to the costs of delivering the standard care pathway
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18 years or over Not resident in care home or nursing home Ambulant Have compatible smartphone/data access (access to a digital device is a necessary prerequisite of system use, and the formative usability study had success in recruiting participants with varying levels of experience with smartphones [18]) Be fluent in English Normally under the care of the Parkinson's service in the participating organisation Participant's healthcare provider in the participating organisation consented to participate in the study Able and willing to provide informed consent Able and willing to comply with intervention requirements Exclusion Criteria: Secondary cause of parkinsonism Significant cognitive impairment or a diagnosis of Parkinson's disease dementia Significant comorbidity, which in the opinion of the chief investigator would preclude safe participation in the study or protocol compliance Previous involvement in development or testing of the NMS Assist system A life expectancy of <6 months Living in residential care facilities Incapable of self-consent In a dependent/unequal relationship with the research or care teams or any PPI representatives
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Edward Meinert, PhD
Phone
01752600600
Email
edward.meinert@plymouth.ac.uk
First Name & Middle Initial & Last Name or Official Title & Degree
Madison Milne-Ives, MSc
Phone
01752600600
Email
madison.milne-ives@plymouth.ac.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Camille Carroll, PhD
Organizational Affiliation
University of Plymouth
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Plymouth
City
Plymouth
State/Province
Devon
ZIP/Postal Code
PL4 6DN
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Only the project leads and associated staff will have access to the research data and healthcare professionals participating in the study will have access only to the data from the PwP and care partners whom they are treating.

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Digitised Home Based Care for Parkinson's Disease

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