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Improving Psychological and Vestibular Health: MINDGAPS (MINDGAPS)

Primary Purpose

Vestibular Hypofunction

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Rehab
Sponsored by
University of Montana
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Vestibular Hypofunction focused on measuring Rehabilitation, mild traumatic brain injury, dynamic visual acuity, gaze stability, postural stability, dizziness, psychological health

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Veteran or Active Duty Military Service Member Ability to stand independently Legally autonomous and able to self-consent Exclusion Criteria: Acute head injury (within the previous 2 months) History of moderate or severe head injury (i.e., loss of consciousness greater than 30 minutes or post-traumatic amnesia greater than 1 day) Current diagnosis of spine disorders in the neck Diagnosis of problems with the arteries in your neck Blindness If you have been diagnosed with abnormal eye movements (also called "ocular motor palsy") If you have previously had a stroke or been diagnosed with a neurodegenerative disorder ( e.g., Parkinson's Disease, Multiple Sclerosis) If you have been previously diagnosed primary vestibular dysfunction ( e.g., congenital peripheral vestibular syndrome) If you have previously been diagnosed with a brain tumor If you are currently receiving physical therapy care for balance or dizziness problems

Sites / Locations

  • Naval Medical Center San DiegoRecruiting
  • University of MontanaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Rehab

Observational

Arm Description

6 weeks of vestibular physical therapy guided by the use of the MINDGAPS decision support system

Normative data development of performance on vestibular measures following mTBI

Outcomes

Primary Outcome Measures

Computerized Dynamic Visual Acuity (cDVA)
computerized measure of functional gaze stability

Secondary Outcome Measures

Instrumented postural sway assessment
instrumented assessment of static postural stability
Video head impulse testing (vHIT)
computerized assessment of vestibulo-ocular reflex function
Functional Gait Assessment (FGA)
The Functional Gait Assessment (FGA) is a 10-item measure that examines dynamic stability during various walking tasks on a marked 6-m (20-ft) length and 12-inch wide walkway. Each item is rated from 0-3 with higher scores indicating better dynamic stability. Tasks within the FGA require head and/or body motion during walking activities which will be assessed using body-worn 3D inertial measurement units
Dizziness Handicap Inventory (DHI)
The DHI is a self assessment inventory designed to evaluate the self-perceived handicap effects imposed by dizziness or unsteadiness and has documented test-retest and internal consistency reliability. The DHI consists of 25 questions subgroup into functional, emotional, and physical components. The total score ranges from 0-100, with higher scores indicating greater handicap.
Life Space Mobility Assessment (LSA)
patient reported questionnaire examining community mobility. The maximum possible score is 40 with higher scores indicating better life space mobility.
Role Participation Questionnaire
patient reported questionnaire assessing participant role in society. The questionnaire asks 17 questions with lower scores indicating greater societal role.
General Well Being Scale
patient reported questionnaire assessing psychological health. Consists of 18 questions with scores ranging from 0-110 and higher scores indicating better well-being.
Healthcare Utilization Questionnaire
patient reported questionnaire assessing participants use of healthcare.
Self-Administered Comorbidity Questionnaire (SCQ)
patient reported questionnaire assessing health related problems, treatment and limitations.
Military Service Information (MSI)
patient reported questionnaire inquiring about military service
Ohio State University Head Injury History
patient reported questionnaire assessing injuries to head and neck
Primary Care 5-Item PTSD Screen
patient reported questionnaire to identify individuals with probable PTSD
Visual Analogy Scale of Dizziness and Unsteadiness
patient report of severity of dizziness and unsteadiness. Participants are asked to draw a single line on a 10 cm line with a higher number indicating greater dizziness or unsteadiness.
High-Level Mobility Assessment (HiMT)

Full Information

First Posted
August 3, 2023
Last Updated
August 9, 2023
Sponsor
University of Montana
Collaborators
United States Naval Medical Center, San Diego, Congressionally Directed Medical Research Programs
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1. Study Identification

Unique Protocol Identification Number
NCT05986279
Brief Title
Improving Psychological and Vestibular Health: MINDGAPS
Acronym
MINDGAPS
Official Title
Improving Psychological and Vestibular Health Using a Novel Intervention: The Making Informed Decisions in Gaze and Postural Stability (MINDGAPS) System
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 30, 2023 (Anticipated)
Primary Completion Date
September 29, 2027 (Anticipated)
Study Completion Date
September 29, 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Montana
Collaborators
United States Naval Medical Center, San Diego, Congressionally Directed Medical Research Programs

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
The purpose of this study is twofold: 1) Develop norms for measures of inner ear function and psychological health, and 2) Examine the feasibility of using the MINDGAPS system (a remote monitoring system) to track progress during physical therapy or rehabilitation for inner ear problems following a concussion or mild Traumatic Brain Injury.
Detailed Description
The intersection between vestibular disturbance and psychological health provides a unique clinical opportunity to address both the modifiable symptoms of vestibular disturbance as well as psychological health. This project aims to advance our understanding of the causal link between vestibular disturbance and poor psychological health and aligns directly with the Traumatic Brain Injury and Psychological Health Research Program (Funding Opportunity: W81XWH-21-TBIPHRP-TRA). Specifically, the proposed research is responsive to each of the three focus areas: Understand- this project is designed to advance the understanding of an established link between vestibular disturbance (e.g., dizziness and poor balance) and poor psychological health (e.g., anxiety, depression, and social isolation) in survivors of mild traumatic brain injury (mTBI). Prevent- the MINDGAPS system allows for precise assessment of dynamic visual acuity (computerized dynamic visual acuity [cDVA]) and postural sway (instrumented balance accelerometry measure [iBAM]), two objective and extensively validated surrogates of vestibular health. Additionally, MINDGAPS uses these measures to inform care decisions via a user-friendly web application. Treat- vestibular assessment is key to effective vestibular care, as it allows for personalization of treatment programs and monitoring progress over time. Objective/Hypothesis: The overall objective of this project is two-fold: 1) Test the preliminary efficacy of the MINDGAPS system to improve psychological health and vestibular disturbance in active-duty and Veteran Service Members (SM) with history of mTBI and 2) refine the MINDGAPS system by developing military-specific normative data and using Community-Based Participatory Research (CBPR) to incorporate the lived experiences of mTBI survivors, their caregivers, and clinicians in the design of the MINDGAPS technology and intervention. Specific Aims: Specific Aim 1 (Preliminary Efficacy): Examine the preliminary efficacy of the MINDGAPS system to improve psychological and vestibular health in active-duty and Veteran SM with sub-acute and chronic mTBI. Specific Aim 2 (Military-specific Normative Data): Collect a cross-sectional sample of cDVA, iBAM, and other relevant measures in active-duty and Veteran Service Members across three different stages of mTBI-no diagnosed history of mTBI, sub-acute mTBI (2-6 months), and chronic mTBI (>6 months)-for the development of normative values in military-specific populations. Specific Aim 3 (Refinement of MINDGAPS): Utilize CBPR to refine and improve the MINDGAPS system for different stakeholders (SM, caregivers, and clinicians) and position MINDGAPS for examination in a large-scale clinical trial as well as translation into clinical practice. Study Design: Aim 1: Using a single-cohort (N=36) double-baseline design, all participants will be tested twice during a no-intervention baseline period, then once following a 6-week course of vestibular training with the MINDGAPS system. Efficacy will be determined by comparing change during the baseline period to change over the course of the intervention period. Aim 2: A large sample of active-duty and Veteran SM (N=300) will be tested in a single, cross-sectional assessment to build military-specific normative vestibular data. Aim 3: We will use a convergent mixed-methods analysis of study participant feedback, in combination with quantitative results and stakeholder engagement, to drive refinement of the MINDGAPS system throughout the study period. Impact: Signs of vestibular disturbance are the most commonly reported symptoms following mTBI, and vestibular disturbance is causally implicated in the development of poor psychological health following mTBI. Interventions aimed at improving vestibular disturbance can improve debilitating symptoms such as poor balance and dizziness. The completion of this study will move MINDGAPS to a technology readiness level of 8, preparing it to be studied in a large clinical trial in the next phase of work. Relevance to Military Health: Interventions aimed at improving vestibular disturbance would have profound impacts on both active-duty SM (inability to visually focus during dynamic tasks- e.g., field of fire) and Veterans (increased risk of falls). Furthermore, the MINDGAPS system enables rapid and precise assessment of vestibular functioning at low cost and therefore has tremendous potential to enhance the delivery of clinical services within a number of active-duty environments including far-forward military settings or Veterans living in rural areas.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vestibular Hypofunction
Keywords
Rehabilitation, mild traumatic brain injury, dynamic visual acuity, gaze stability, postural stability, dizziness, psychological health

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
One group is enrolled into a longitudinal, single group intervention using vestibular rehab. The other group is enrolled as a cross-sectional observational assessment used for developing normative data.
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
500 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Rehab
Arm Type
Experimental
Arm Description
6 weeks of vestibular physical therapy guided by the use of the MINDGAPS decision support system
Arm Title
Observational
Arm Type
No Intervention
Arm Description
Normative data development of performance on vestibular measures following mTBI
Intervention Type
Other
Intervention Name(s)
Rehab
Intervention Description
6 weeks of vestibular rehabilitation guided by the MINDGAPS decision support system
Primary Outcome Measure Information:
Title
Computerized Dynamic Visual Acuity (cDVA)
Description
computerized measure of functional gaze stability
Time Frame
through study completion, an average of 12 weeks
Secondary Outcome Measure Information:
Title
Instrumented postural sway assessment
Description
instrumented assessment of static postural stability
Time Frame
through study completion, an average of 12 weeks
Title
Video head impulse testing (vHIT)
Description
computerized assessment of vestibulo-ocular reflex function
Time Frame
through study completion, an average of 12 weeks
Title
Functional Gait Assessment (FGA)
Description
The Functional Gait Assessment (FGA) is a 10-item measure that examines dynamic stability during various walking tasks on a marked 6-m (20-ft) length and 12-inch wide walkway. Each item is rated from 0-3 with higher scores indicating better dynamic stability. Tasks within the FGA require head and/or body motion during walking activities which will be assessed using body-worn 3D inertial measurement units
Time Frame
through study completion, an average of 12 weeks
Title
Dizziness Handicap Inventory (DHI)
Description
The DHI is a self assessment inventory designed to evaluate the self-perceived handicap effects imposed by dizziness or unsteadiness and has documented test-retest and internal consistency reliability. The DHI consists of 25 questions subgroup into functional, emotional, and physical components. The total score ranges from 0-100, with higher scores indicating greater handicap.
Time Frame
through study completion, an average of 12 weeks
Title
Life Space Mobility Assessment (LSA)
Description
patient reported questionnaire examining community mobility. The maximum possible score is 40 with higher scores indicating better life space mobility.
Time Frame
through study completion, an average of 12 weeks
Title
Role Participation Questionnaire
Description
patient reported questionnaire assessing participant role in society. The questionnaire asks 17 questions with lower scores indicating greater societal role.
Time Frame
through study completion, an average of 12 weeks
Title
General Well Being Scale
Description
patient reported questionnaire assessing psychological health. Consists of 18 questions with scores ranging from 0-110 and higher scores indicating better well-being.
Time Frame
through study completion, an average of 12 weeks
Title
Healthcare Utilization Questionnaire
Description
patient reported questionnaire assessing participants use of healthcare.
Time Frame
through study completion, an average of 12 weeks
Title
Self-Administered Comorbidity Questionnaire (SCQ)
Description
patient reported questionnaire assessing health related problems, treatment and limitations.
Time Frame
through study completion, an average of 12 weeks
Title
Military Service Information (MSI)
Description
patient reported questionnaire inquiring about military service
Time Frame
through study completion, an average of 12 weeks
Title
Ohio State University Head Injury History
Description
patient reported questionnaire assessing injuries to head and neck
Time Frame
through study completion, an average of 12 weeks
Title
Primary Care 5-Item PTSD Screen
Description
patient reported questionnaire to identify individuals with probable PTSD
Time Frame
through study completion, an average of 12 weeks
Title
Visual Analogy Scale of Dizziness and Unsteadiness
Description
patient report of severity of dizziness and unsteadiness. Participants are asked to draw a single line on a 10 cm line with a higher number indicating greater dizziness or unsteadiness.
Time Frame
through study completion, an average of 12 weeks
Title
High-Level Mobility Assessment (HiMT)
Time Frame
through study completion, an average of 12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Veteran or Active Duty Military Service Member Ability to stand independently Legally autonomous and able to self-consent Exclusion Criteria: Acute head injury (within the previous 2 months) History of moderate or severe head injury (i.e., loss of consciousness greater than 30 minutes or post-traumatic amnesia greater than 1 day) Current diagnosis of spine disorders in the neck Diagnosis of problems with the arteries in your neck Blindness If you have been diagnosed with abnormal eye movements (also called "ocular motor palsy") If you have previously had a stroke or been diagnosed with a neurodegenerative disorder ( e.g., Parkinson's Disease, Multiple Sclerosis) If you have been previously diagnosed primary vestibular dysfunction ( e.g., congenital peripheral vestibular syndrome) If you have previously been diagnosed with a brain tumor If you are currently receiving physical therapy care for balance or dizziness problems
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Brian Loyd, PhD
Phone
406-243-4015
Email
Brian.loyd@umontana.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Andy Kittelson, PhD
Phone
406-243-4015
Email
Andy.kittelson@umontana.edu
Facility Information:
Facility Name
Naval Medical Center San Diego
City
San Diego
State/Province
California
ZIP/Postal Code
92134
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Trevor Kingsbury
Phone
619-532-7136
Email
trevor.d.kingsbury.civ@health.mil
Facility Name
University of Montana
City
Missoula
State/Province
Montana
ZIP/Postal Code
59812
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Brian Loyd, PhD
Phone
406-243-4015
Email
brian.loyd@umontana.edu
First Name & Middle Initial & Last Name & Degree
Andy Kittelson, PhD
Phone
406-243-4015
Email
andy.kittelson@umontana.edu

12. IPD Sharing Statement

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Improving Psychological and Vestibular Health: MINDGAPS

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