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Multiple Sclerosis Falls Insight Track (MS FIT)

Primary Purpose

Multiple Sclerosis

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
MS FIT: Falls Insight Track
Sponsored by
University of California, San Francisco
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Multiple Sclerosis focused on measuring Multiple Sclerosis, MS, Falls, Falling

Eligibility Criteria

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

Inclusion Criteria: Diagnosis of MS (relapsing or progressive) by 2017 McDonald Criteria18 Ages 18 and above Any MS therapy, or no treatment California resident to enable clinical telemedicine visits if warranted during the study visit EDSS 2.5-7.0 (moderate to severe impairment, 7= wheelchair but independent transfers) Fall risk, based on MSWS-12 score and previous report of a fall (Hopkins grade ≥1) Technological criteria: availability of Wi-Fi in the home or workspace for connectivity. Exclusion Criteria: Cognitive dexterity or visual impairment that, in the opinion of the study neurologist (RB), would put the participant at risk or limit their ability to comply with the study protocol Inability to provide informed consent

Sites / Locations

  • University of California, San FranciscoRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

MS FIT: Falls Insight Track

Arm Description

Participants in this arm will receive 12 months use of MS FIT mobile tool intervention

Outcomes

Primary Outcome Measures

Percentage of patients initially use the tool (Adoption)
This will be measured by calculating the percentage of patients who use the tool during the initial month of the study, and by the percentage of patient-clinical dyads who use the tool during the clinical visit
Percentage of patient-clinician encounters initially use the tool (Adoption)
This will be measured by calculating the percentage of patient-clinical dyads who use the tool during the clinical visit.
Percentage of patients who continue to use the tool (Engagement)
This will calculate the percentage of patients who continued to use the patient-facing tool at least quarterly
Percentage of patient-clinician encounters use the tool during the 12-month visit (Engagement)
This will be calculated by the percentage of the clinician-patient dyads in Arm 1 who use the in-visit dashboard at the 12-month clinical visit.
Percentage of patients who respond to fall prompts (Adherence)
Adherence will be measured by the percentage of falls reporting prompts adhered to per participant, as well as percentage of participants adhering to >75% falls prompts

Secondary Outcome Measures

Full Information

First Posted
April 17, 2023
Last Updated
April 27, 2023
Sponsor
University of California, San Francisco
Collaborators
National Institutes of Health (NIH), National Library of Medicine (NLM)
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1. Study Identification

Unique Protocol Identification Number
NCT05837949
Brief Title
Multiple Sclerosis Falls Insight Track
Acronym
MS FIT
Official Title
Multiple Sclerosis Falls Insight Track: A Personal Health Library to Reduce Falls in Patients With Multiple Sclerosis
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 12, 2023 (Actual)
Primary Completion Date
April 12, 2026 (Anticipated)
Study Completion Date
April 12, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, San Francisco
Collaborators
National Institutes of Health (NIH), National Library of Medicine (NLM)

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
The purpose of this study is to develop an application: MS Falls Insight Track (MS FIT) which allows patients to log their falls and near falls, view their MS relevant data and responses to the clinic intake survey as well as communicate with their care team about falls and receive educational material on falls prevention.
Detailed Description
Falls occur in >50% patients with multiple sclerosis (MS), worsen participation in daily life and increase healthcare costs. To date there are no established, accessible, tools to evaluate and reduce fall risk. MS Falls InsightTrack is a live personal health library that combines a patient's falls-relevant clinical indicators (from the electronic health record, EHR) with patient-generated data (PGD) from commercial wearable tools and patient-reported outcomes (PROs) and community-level data (sociodemographic data from University of California, San Francisco (UCSF) Health Atlas combined with MS-specific resources from the National MS Society). The tool will track falls/near-falls in real- time and report changes in status that require intervention. It will offer customized action prompts to support fall reduction through a behaviorally informed approach. It will be accessed in the clinic and in the patient's home. Technological features. The tool will be accessible, extensible and scalable. The investigators will use modern technologies and industry standards (e.g back-end: Python, flask framework, PostgreSQL; front-end: HTML, CSS, JavaScript and d3.js). The tool will launch from Epic via SMART on FHIR, and will communicate with patients using MyChart. Qualifications of team and setting. The UCSF MS Center is a leading clinical research center in the digital space. Our sub-leads are experts in all aspects of the study (digital technology, human-centered design, implementation science, health literacy) with a varied and experienced Stakeholder Advisory Group. Scientific plan. In Aim 1 (design), the investigators will use a Human-Centered Design approach, engaging 20 patients with MS, clinicians and stakeholders in a series of focus groups, to identify the critical data, devices, visualizations, resources, workflows and accessibility/digital divide considerations for the tool, and the key interventions likely to promote the COM-B model of behavioral change to reduce fall risk. Our key outcomes will be perceived effectiveness, ease of use and likability. In Aim 2 (evaluate feasibility), investigators will deploy MS Falls Insight Track in 100 diverse adults with MS who are at risk for falls. Participants will wear a Fitbit. The tool will be used by patients in their homes and by clinicians during clinical encounters. The investigators will use an implementation science approach. Our key outcomes will be study retention, tool uptake and sustained use. The investigators will explore impact on fall risk. In Aim 3 (test generalizability) investigators will conduct focus groups with patients with other conditions where falls are common (Orthopedics, Parkinson's Disease, Geriatrics) to understand additional data and design features required to promote generalizability. Our key outcomes will parallel those in Aim 1. Innovation and Broader Significance. MS Falls Insight Track is a unique, comprehensive, accessible personal health library that can be deployed in larger efficacy trials for falls reduction. Beyond this clinical use case, the closed-loop approach of delivering PGD to the care system and back to the patient, interpreted and actionable, using scalable technology, represents a significant innovation that can sequentially expand the number of wearables, conditions and clinics in which patients and clinical investigators can ask their own questions of PGD.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis
Keywords
Multiple Sclerosis, MS, Falls, Falling

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
All participants will be given the MS FIT tool intervention
Masking
None (Open Label)
Allocation
N/A
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
MS FIT: Falls Insight Track
Arm Type
Experimental
Arm Description
Participants in this arm will receive 12 months use of MS FIT mobile tool intervention
Intervention Type
Behavioral
Intervention Name(s)
MS FIT: Falls Insight Track
Intervention Description
Participants will respond to a set of surveys every two weeks to increase communication on falls with their clinician.
Primary Outcome Measure Information:
Title
Percentage of patients initially use the tool (Adoption)
Description
This will be measured by calculating the percentage of patients who use the tool during the initial month of the study, and by the percentage of patient-clinical dyads who use the tool during the clinical visit
Time Frame
6 months
Title
Percentage of patient-clinician encounters initially use the tool (Adoption)
Description
This will be measured by calculating the percentage of patient-clinical dyads who use the tool during the clinical visit.
Time Frame
6 months
Title
Percentage of patients who continue to use the tool (Engagement)
Description
This will calculate the percentage of patients who continued to use the patient-facing tool at least quarterly
Time Frame
12 months
Title
Percentage of patient-clinician encounters use the tool during the 12-month visit (Engagement)
Description
This will be calculated by the percentage of the clinician-patient dyads in Arm 1 who use the in-visit dashboard at the 12-month clinical visit.
Time Frame
12 months
Title
Percentage of patients who respond to fall prompts (Adherence)
Description
Adherence will be measured by the percentage of falls reporting prompts adhered to per participant, as well as percentage of participants adhering to >75% falls prompts
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of MS (relapsing or progressive) by 2017 McDonald Criteria18 Ages 18 and above Any MS therapy, or no treatment California resident to enable clinical telemedicine visits if warranted during the study visit EDSS 2.5-7.0 (moderate to severe impairment, 7= wheelchair but independent transfers) Fall risk, based on MSWS-12 score and previous report of a fall (Hopkins grade ≥1) Technological criteria: availability of Wi-Fi in the home or workspace for connectivity. Exclusion Criteria: Cognitive dexterity or visual impairment that, in the opinion of the study neurologist (RB), would put the participant at risk or limit their ability to comply with the study protocol Inability to provide informed consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Riley Bove, MD
Phone
415.595.2795
Email
riley.bove@ucsf.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Jaeleene Wijangco, BS
Phone
415.353.2174
Email
jaeleene.wijangco@ucsf.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Riley Bove, MD
Organizational Affiliation
University of California, San Francisco
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of California, San Francisco
City
San Francisco
State/Province
California
ZIP/Postal Code
94158
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Riley Bove, MD
Phone
415-595-2795
Email
riley.bove@ucsf.edu
First Name & Middle Initial & Last Name & Degree
Jaeleene Wijangco, BS
Phone
415.353.2174
Email
jaeleene.wijangco@ucsf.edu
First Name & Middle Initial & Last Name & Degree
Riley Bove, MD

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The deidentified dataset will be shared with qualified collaborators upon request, provision of CITI and other certifications, and data sharing agreement. We will share the results, once the data are complete and analyzed, with the scientific community and patient/clinician participants through abstracts, presentations and manuscripts.
IPD Sharing Time Frame
6 months post trial
IPD Sharing Access Criteria
Qualified collaborators upon request, provision of CITI and other certifications, and data sharing agreement

Learn more about this trial

Multiple Sclerosis Falls Insight Track

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