Telehealth in Lewy Body Dementia
Primary Purpose
Lewy Body Dementia With Behavioral Disturbance, Lewy Body Parkinson Disease, Lewy Body Disease
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Tele-neurohub
Sponsored by
About this trial
This is an interventional health services research trial for Lewy Body Dementia With Behavioral Disturbance
Eligibility Criteria
Participant with Lewy Body Dementia (LBD) Inclusion Criteria:
- LBD diagnosis by a dementia or movement disorders specialist
- Clinician-determined mild-moderate dementia severity
- Internet access with a Zoom-compatible device
- Caregiver who resides in the patient's home and is willing to participate
- Fluency in English
Healthcare Professional Inclusion Criteria:
- > 1 year of experience with LBD
- Willingness to participate in the study
- Fluency in English
Sites / Locations
- University of FloridaRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Tele-neurohub
Usual care group
Arm Description
This group will receive the tele-neurohub intervention which includes telemedicine appointments with the neurologist, speech therapist, social worker, and nutritionist at baseline, 3 months and 6 months, and PT and OT every 2 weeks for maintenance neuro-rehabilitation.
Receive usual care but will have study visit assessments at baseline and 6 months.
Outcomes
Primary Outcome Measures
Number of completed tele-health visits
Feasibility will be determined by completion of at least 75% telehealth visits by the intervention cohort
Secondary Outcome Measures
Satisfaction assessed by Patient Assessment of Communication of Telehealth questionnaire.
Acceptability will be determined by at least 80% of dyads reporting being "satisfied" or "highly satisfied" on the Patient Assessment of Communication of Telehealth questionnaire.
Appropriateness assessed by Intervention Appropriateness Measure
Appropriateness will be determined by the Intervention Appropriateness Measure, higher scores indicate greater appropriateness
Full Information
NCT ID
NCT05014971
First Posted
August 13, 2021
Last Updated
April 14, 2023
Sponsor
University of Florida
Collaborators
National Institute on Aging (NIA)
1. Study Identification
Unique Protocol Identification Number
NCT05014971
Brief Title
Telehealth in Lewy Body Dementia
Official Title
Multi-Stakeholder Engagement for Interdisciplinary Telehealth in Lewy Body Dementia
Study Type
Interventional
2. Study Status
Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 28, 2022 (Actual)
Primary Completion Date
May 31, 2026 (Anticipated)
Study Completion Date
May 31, 2026 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Florida
Collaborators
National Institute on Aging (NIA)
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Lewy body dementia (LBD) is the 2nd most common neurodegenerative dementia in the US. Optimal care requires an interdisciplinary approach, however often faced barriers include rural residence, limited access to specialists, travel distance, limited awareness of resources, and physical, cognitive, and behavioral impairments making travel to appointments challenging. Delivering interdisciplinary care remotely using video technology has the potential to improve access to care for patients with LBD.
Detailed Description
The purpose of this study is to convert an in-person patient-centric interdisciplinary care model to a virtual platform using stakeholder engagement from individuals with LBD, their caregivers and healthcare providers. Subsequently researchers will conduct a prospective, randomized, controlled pilot study implementing the virtual stakeholder developed interdisciplinary care model (tele-neurohub) for 6 month and assess the implementation outcomes of feasibility, acceptability, and appropriateness of the tele-neurohub model. The research goal is to establish and iteratively improve a virtual interdisciplinary model of care allowing patients with LBD and their caregivers to access sub-specialty care from their home.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lewy Body Dementia With Behavioral Disturbance, Lewy Body Parkinson Disease, Lewy Body Disease
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
tele-neurohub model of care
Masking
None (Open Label)
Allocation
Randomized
Enrollment
106 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Tele-neurohub
Arm Type
Experimental
Arm Description
This group will receive the tele-neurohub intervention which includes telemedicine appointments with the neurologist, speech therapist, social worker, and nutritionist at baseline, 3 months and 6 months, and PT and OT every 2 weeks for maintenance neuro-rehabilitation.
Arm Title
Usual care group
Arm Type
Active Comparator
Arm Description
Receive usual care but will have study visit assessments at baseline and 6 months.
Intervention Type
Behavioral
Intervention Name(s)
Tele-neurohub
Intervention Description
Interdisciplinary care delivered using telemedicine (zoom) technology which includes neurologist, physical, occupational and speech therapy, social worker and dietician.
Primary Outcome Measure Information:
Title
Number of completed tele-health visits
Description
Feasibility will be determined by completion of at least 75% telehealth visits by the intervention cohort
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Satisfaction assessed by Patient Assessment of Communication of Telehealth questionnaire.
Description
Acceptability will be determined by at least 80% of dyads reporting being "satisfied" or "highly satisfied" on the Patient Assessment of Communication of Telehealth questionnaire.
Time Frame
6 months
Title
Appropriateness assessed by Intervention Appropriateness Measure
Description
Appropriateness will be determined by the Intervention Appropriateness Measure, higher scores indicate greater appropriateness
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Participant with Lewy Body Dementia (LBD) Inclusion Criteria:
LBD diagnosis by a dementia or movement disorders specialist
Clinician-determined mild-moderate dementia severity
Internet access with a Zoom-compatible device
Caregiver who resides in the patient's home and is willing to participate
Fluency in English
Healthcare Professional Inclusion Criteria:
> 1 year of experience with LBD
Willingness to participate in the study
Fluency in English
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Bhavana Patel, DO
Phone
352-294-5400
Email
bhavana.patel@neurology.ufl.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Noheli Bedenfield, MHA
Phone
352-733-2419
Email
noheli.gamez@neurology.ufl.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bhavana Patel, DO
Organizational Affiliation
University of Florida
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Florida
City
Gainesville
State/Province
Florida
ZIP/Postal Code
32610
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bhavana Patel, DO
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Telehealth in Lewy Body Dementia
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