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TerminatedNCT03888287PICKUpdated Apr 18, 2023Results posted

Parkinson's Disease Inpatient Clinical Knowledge and Management

An interventional study of Watch Rx system and Parkinson's Disease Inpatient Clinical Knowledge and Management Program in Parkinson Disease, sponsored by Hackensack Meridian Health. Terminated at 1 site in United States. Open to participants aged 22 Years and older. Per ClinicalTrials.gov, last updated 2023-04-18.

Sponsored by Hackensack Meridian Health · Not applicable, Interventional, and Supportive care

Why this study was terminated
Study was put on hold due to COVID and never reopened
Phase
Not applicable
Study type
Interventional
Enrollment
477
Allocation
Non-randomized
Ages
22 Years and older
Sex
All
01

Study summary

This study will focus on patients with Parkinson's Disease in the adult inpatient units of Hackensack University Medical Center. We are measuring the effect of a Parkinson's Disease Inpatient Clinical Knowledge and Management Program on adherence to Parkinson's Disease medication using a Parkinson's Disease Identification Wrist Band, smartwatch and medication schedule card

Read the detailed description

Parkinson's Disease (PD), the second-most common neurodegenerative disorder and is ranked the fourteenth leading cause of death. PD prevalence rate in the United States is estimated to be approximately 0.3% and is ranked the fourteenth leading cause of death (CDC, 2013). Depending on the methodology, the national prevalence data on PD is varied and insufficient. PD is projected to increase by 4% to 5% in age 65 and over 85 years respectively and is associated with a high economic burden exceeding $14.4 billion per year.

Admission to the hospital is identified as a major risk factor due to imprecise timing of medication administration, disruption of sleep pattern, dietary changes, and unfamiliarity of the hospital environment which all contribute to the exacerbation of PD symptoms. Parkinson's disease Foundation, 2015). Hospital length of stay for patients with PD is 1.45 times higher in comparison to non- PD patients.

A study by Chou et al., (2011) involving 51 worldwide National Parkinson Foundation Centers found 94% of centers were not confident in the care and knowledge hospital professionals provided specific to: PD medications, complex drug interactions, contraindications and precise timing of medication administration. Hospital co-morbidities could be improved or prevented by adjustment of PD medication and medication adherence, critical in decreasing hospital length of stay.

The retrospective phase will be a data collection of adult patients admitted with a primary and secondary diagnosis of Parkinson's disease during January - June 2015 (6 month period). There will be 150 patients selected by the principal investigator(s) from chart review. In addition, the clinicians chosen for the study will complete a Parkinson's Disease Knowledge Assessment Survey.

The prospective phase will begin after completion of the Parkinson's Disease Inpatient Clinical Knowledge and Management Program for staff nurses, advanced practice nurses (APN), nursing assistants, patient care technicians, case managers, adult inpatient physician assistants, pharmacists, occupational therapists, physical therapists, nurse educators, and dietitians. There will be 150 patients selected from the adult inpatient units by the principal investigator(s) that meet the inclusion criteria and confirm through an informed consent that they will participate in the study.

The selected patients will be registered in a WatchRx interface via website URL by the Principal Investigator(s) and the Transition of Care(TC) Pharmacist and required to wear a Watch Rx smartwatch for the duration of their hospitalization. The Watch Rx Interface will store all medical information, necessary treatments, and daily clinical care for the patient which is synchronized to the smartwatch on the patient's wrist. The smartwatch will send alerts to the patient's assigned nurse's iPad through a Watch Rx app for medication administration, missed PD medications, battery conditions, and enables messaging between the primary nurse and the patient.

The WatchRx smartwatch will remind when it is time to take the medication. If the Parkinson's Disease medication is not administered, it sends missed medication reminder alerts to the nurse. For fixed time medication, the reminder is every 3 minutes up to 10 minutes.

During the prospective phase, the research team will collect data from multiple sources such as the Watch Rx system, EPIC Hyperspace, and Case Report forms over a 6 month study period. The data will be calculated by using statistical analysis for the continuous variables and categorical variables identified from the collection of data. All study data will be imported into SAS software where data programming will be utilized to flag and generate queries on out-of-range data issues until they are resolved. All analysis will be performed using SAS version 9.4 (SAS Institute Inc. Cary, North Carolina, USA Data will be handled in a confidential manner to meet mandated IT Security standards and to prevent loss of privacy. All electronic files will be stored in an encrypted and password-protected database on a secure medical center server. Only co-investigators, advanced practice nurses, and the data coordinator who contact the subjects will have access to information linked to subject identifiers.

This study will improve timely administration of medications to PD patients. Patients enrolled in the study will have direct monitoring of their medication compliance and adherence. Patients participating in the registry will be gain information from the current research and possibly create a support group amongst themselves. This study will improve knowledge of Parkinson's disease amongst clinicians and better medication management of PD patients

02

Conditions studied

  • Parkinson Disease

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Keywords

  • PICK study
  • Impact of Watch Rx
03

In context

Parkinson Disease

4,583 studies on the registry are indexed under Parkinson Disease; 1,097 are open to participants now.

This study's enrollment of 477 is above the median of 40 across 3,365 interventional studies indexed under Parkinson Disease.

Browse Parkinson Disease studies →

Lead sponsor

Hackensack Meridian Health is the lead sponsor of 113 studies on the registry; 28 are open to participants now.

Of its 17 completed or terminated interventional studies of FDA-regulated products, 12 (71%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
22 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adult patients diagnosed with primary and secondary diagnosis of Parkinson's disease
  • Patient 22 years old and older
  • Patients admitted to inpatient units
  • Patient who are verbally informed and agree to participate in the study

Exclusion criteria

Exclusion Criteria:

  • Patients less than or equal to 21 years of age
  • Patients who refuse to wear the PD wrist band.
  • Patients who verbally refuse enrollment in the PD registry.
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Non-randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
477 participants (actual)

Study arms

  • Experimental
    Retrospective Phase

    Patients with Parkinson disease before completion of the Parkinson's Disease Inpatient Clinical Knowledge and Management Program.

    Device: Watch Rx system

  • Experimental
    Prospective Phase-Watch Rx system

    Patients after completion of the Parkinson's Disease Inpatient Clinical Knowledge and Management Program who are also assigned to a WatchRx system

    Device: Watch Rx system · Other: Parkinson's Disease Inpatient Clinical Knowledge and Management Program

  • Experimental
    Retrospective Phase - Clinicians

    Clinicians, including physician's assistant, advanced practice nurses, staff nurses, nurse educators, case managers, dietitians pharmacists physical therapist and occupational therapist before completion of the Parkinson's Disease Inpatient Clinical Knowledge and Management Program.

    Other: Parkinson's Disease Inpatient Clinical Knowledge and Management Program

  • Experimental
    Prospective Phase - Clinicians

    Clinicians, including physician's assistant, advanced practice nurses, staff nurses, nurse educators, case managers, dietitians pharmacists physical therapist and occupational therapist after completion of the Parkinson's Disease Inpatient Clinical Knowledge and Management Program.

    Other: Parkinson's Disease Inpatient Clinical Knowledge and Management Program

Interventions

  • DeviceWatch Rx system

    The Watch Rx system consists of a Watch Rx smartwatch, Watch Rx application and a WatchRx Web Interface. The Watch Rx smartwatch will be worn on the patient's wrist. The smart watch will send alerts to the caregivers through the Watch Rx app when it is time to administer the medication. The Web Interface will be used to store the medical documentations

  • OtherParkinson's Disease Inpatient Clinical Knowledge and Management Program

    Parkinson's Disease Inpatient Clinical Knowledge and Management Program educates clinical staff and measures difference in knowledge of medication adherence and compliance for hospitalized Parkinson's Disease patients

06

What researchers measure

Primary outcomes

  1. Clinician's Parkinson's Disease Knowledge Assessment Survey Scores

    Clinician's Parkinson's Disease Knowledge Assessment Survey scores before and after the Parkinson's Disease Inpatient Clinical Knowledge and Management Program. A 20-question survey was administered to PD clinicians for a group measurement of PD knowledge. Scores ranged from 0 - 100% and reflected the percentage of clinicians who correctly answered the question. If 70% or more clinicians correctly answered the question, the group was considered knowledgeable on that topic; if \<70% of clinicians responded incorrectly, they were considered not knowledgeable on the information that the question assessed. Survey questions addressed three PD areas: 1) medication/treatment, 2) symptoms/diagnosis, and 3) epidemiology/pathophysiology.

    Time frame: 6 months

Secondary outcomes

  1. Number of PD Medications Administered on Time (15 Minute Window)

    The number of Parkinson's Disease (PD) medications administered within the 15-minute timeframe at baseline

    Time frame: within 15 minutes post PD medication administration time

  2. Number of Patients With Contraindicated Medications Administered.

    Measure the number of patients who were adminstered contraindicated medications

    Time frame: 6 months

  3. Number Patients With Falls, Falls With Injury, Positive CAM/Mini-cog

    The number of falls, number of falls with injury, and number of patients with positive Confusion Assessment Method (CAM)/Mini-Cog scores) in hospitalized patients. Mini-cog is performed on all admitted patients 65 years and older and is a quick screening for "cognitive vital sign" and early dementia detection. The scale classifies patients as being positive or negative for dementia. The Confusion Assessment Method (CAM) is performed on all adult admissions at the time of admission with reporting 1) every shift if the first test is positive, or 2) daily if the first test is negative. It improves the detection and recognition of delirium accurately and quickly in clinical and research settings. CAM is documentation of observed patient behavior during brief, structured interviews according to classification of positive or negative for dementia. There are no numerical (minimum or maximum) values assigned.

    Time frame: 6 Months

  4. Length of Stay in Hospitalized Parkinson's Disease Patients.

    Average length of stay in hospitalized Parkinson's Disease patients

    Time frame: 6 months

  5. Number of PD Medications Administered on Time (Within 15 Minute Window)

    Track the difference that the WatchRx system has on scheduled PD medication administration time versus actual PD medication administration time

    Time frame: 15 minutes post assigned medication administration time.

  6. Number of PD Medication Errors After Using the WatchRX System

    The number of contraindicated medications administered to Parkinson's disease patients after using the WatchRX system

    Time frame: 6 Months

  7. Number of Falls, Falls Within Injury, Positive CAM Scores, and Positive Mini-Cog Scores After Using the WatchRX System

    The number of falls, number of falls with injury, number of positive CAM scores, and number of positive Mini-Cog scores after using the WatchRX system.

    Time frame: 6 months

  8. Length of Stay With the WatchRx System

    Parkinson's disease patients' length of stay after using the WatchRx system

    Time frame: 6 months

07

Results

Posted Mar 16, 2023
Limitations and caveats
Prospective enrollment did not occur due to the COVID-19 pandemic, patients were not admitted for elective surgeries. Results of the clinician education were only reported in aggregate.

Participant flow

Participant flow — Overall Study
MilestoneRetrospective PhaseProspective Phase-Watch Rx SystemRetrospective Phase - CliniciansProspective Phase - Clinicians
Started131026680
Completed131026680
Not completed0000

Outcome measures

PrimaryClinician's Parkinson's Disease Knowledge Assessment Survey Scores

Clinician's Parkinson's Disease Knowledge Assessment Survey scores before and after the Parkinson's Disease Inpatient Clinical Knowledge and Management Program. A 20-question survey was administered to PD clinicians for a group measurement of PD knowledge. Scores ranged from 0 - 100% and reflected the percentage of clinicians who correctly answered the question. If 70% or more clinicians correctly answered the question, the group was considered knowledgeable on that topic; if \<70% of clinicians responded incorrectly, they were considered not knowledgeable on the information that the question assessed. Survey questions addressed three PD areas: 1) medication/treatment, 2) symptoms/diagnosis, and 3) epidemiology/pathophysiology.

Time frame:
6 months
Reported as:
Mean · average knowledge score
Clinician's Parkinson's Disease Knowledge Assessment Survey Scores
average knowledge scoreClinicians' Knowledge Before Educational InterventionClinicians' Knowledge After Educational Intervention
Clinician's Parkinson's Disease Knowledge Assessment Survey Scores68.50 (0 to 100)78.75 (0 to 100)
SecondaryNumber of PD Medications Administered on Time (15 Minute Window)

The number of Parkinson's Disease (PD) medications administered within the 15-minute timeframe at baseline

Time frame:
within 15 minutes post PD medication administration time
Reported as:
Number · number of PD meds administered in 15 min
Number of PD Medications Administered on Time (15 Minute Window)
number of PD meds administered in 15 minRetrospective Patient Outcomes
Number of PD Medications Administered on Time (15 Minute Window)678
SecondaryNumber of Patients With Contraindicated Medications Administered.

Measure the number of patients who were adminstered contraindicated medications

Time frame:
6 months
Reported as:
Count of participants · Participants
Number of Patients With Contraindicated Medications Administered.
ParticipantsRetrospective Patient Outcomes
Number of Patients With Contraindicated Medications Administered.21
SecondaryNumber Patients With Falls, Falls With Injury, Positive CAM/Mini-cog

The number of falls, number of falls with injury, and number of patients with positive Confusion Assessment Method (CAM)/Mini-Cog scores) in hospitalized patients. Mini-cog is performed on all admitted patients 65 years and older and is a quick screening for "cognitive vital sign" and early dementia detection. The scale classifies patients as being positive or negative for dementia. The Confusion Assessment Method (CAM) is performed on all adult admissions at the time of admission with reporting 1) every shift if the first test is positive, or 2) daily if the first test is negative. It improves the detection and recognition of delirium accurately and quickly in clinical and research settings. CAM is documentation of observed patient behavior during brief, structured interviews according to classification of positive or negative for dementia. There are no numerical (minimum or maximum) values assigned.

Time frame:
6 Months
Reported as:
Count of participants · Participants
Number Patients With Falls, Falls With Injury, Positive CAM/Mini-cog
ParticipantsRetrospective Patient Outcomes
Number of falls1
Number of falls with injury0
Number of patients with positive CAM scores47
Number of patients with abnormal mini-cog scores45
SecondaryLength of Stay in Hospitalized Parkinson's Disease Patients.

Average length of stay in hospitalized Parkinson's Disease patients

Time frame:
6 months
Reported as:
Mean · days
Length of Stay in Hospitalized Parkinson's Disease Patients.
daysRetrospective Patient Outcomes
Length of Stay in Hospitalized Parkinson's Disease Patients.6.1 ± 6.6
SecondaryNumber of PD Medications Administered on Time (Within 15 Minute Window)

Track the difference that the WatchRx system has on scheduled PD medication administration time versus actual PD medication administration time

Time frame:
15 minutes post assigned medication administration time.

No measurements were reported for this outcome.

SecondaryNumber of PD Medication Errors After Using the WatchRX System

The number of contraindicated medications administered to Parkinson's disease patients after using the WatchRX system

Time frame:
6 Months

No measurements were reported for this outcome.

SecondaryNumber of Falls, Falls Within Injury, Positive CAM Scores, and Positive Mini-Cog Scores After Using the WatchRX System

The number of falls, number of falls with injury, number of positive CAM scores, and number of positive Mini-Cog scores after using the WatchRX system.

Time frame:
6 months

No measurements were reported for this outcome.

SecondaryLength of Stay With the WatchRx System

Parkinson's disease patients' length of stay after using the WatchRx system

Time frame:
6 months

No measurements were reported for this outcome.

Adverse events

Collected over Up to 6 months for patient and clinician participants in the Retrospective Phase. Duration of the educational intervention including pre and post-surveys for clinicians in the Prospective Phase, overall duration 5 months. Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Retrospective Phase - Watch Rx System0/131 (0%)0/131 (0%)0/131 (0%)
Prospective Phase - Watch Rx System———
Retrospective Phase - Clinicians0/266 (0%)0/266 (0%)0/266 (0%)
Prospective Phase - Clinicians0/80 (0%)0/80 (0%)0/80 (0%)

Baseline characteristics

No one was enrolled in the patient prospective phase.

Age, Customized
Age, Customized(years)Retrospective PhaseProspective Phase-Watch Rx SystemTotal
Mean76 ± 14.4—76 ± 14.4
Sex: Female, Male
Sex: Female, Male(Participants)Retrospective PhaseProspective Phase-Watch Rx SystemTotal
Female54054
Male77077
Ethnicity (NIH/OMB)
Ethnicity (NIH/OMB)(Participants)Retrospective PhaseProspective Phase-Watch Rx SystemTotal
Hispanic or Latino23023
Not Hispanic or Latino1070107
Unknown or Not Reported101
Race (NIH/OMB)
Race (NIH/OMB)(Participants)Retrospective PhaseProspective Phase-Watch Rx SystemTotal
American Indian or Alaska Native000
Asian404
Native Hawaiian or Other Pacific Islander000
Black or African American404
White1060106
More than one race000
Unknown or Not Reported17017
Region of Enrollment
Region of Enrollment(participants)Retrospective PhaseProspective Phase-Watch Rx SystemTotal
United States131—477
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Study locations

1 site
  • Hackensack University Medical Center
    Hackensack, New Jersey 07601, United States
09

References and documents

Study documents

  • Protocol and statistical analysis plan · May 9, 2019

Documents are hosted by the registry — open the source record to download them.

10

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Aug 2018 to primary completion in Jan 2022, 41 months.

Results were first posted in Mar 2023, 1 year 2 months after primary completion.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 1, 2018
First posted
Mar 25, 2019
StartActual
Aug 1, 2018
Primary completionActual
Jan 3, 2022
CompletionActual
Jan 3, 2022
Results first posted
Mar 16, 2023
Last update
Apr 18, 2023
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 18, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03888287
Responsible party
Sponsor
First posted
Mar 25, 2019
Start date
Aug 1, 2018
Primary completion
Jan 3, 2022
Completion
Jan 3, 2022
Results posted
Mar 16, 2023
Last update
Apr 18, 2023

Study contacts

Azmi Hooman, MD
principal investigator · Hackensack Meridian Health
Mohammed Quadri, MD, MBA
principal investigator · Hackensack Meridian Health

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

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