ClinicalTrials.gg
CompletedNCT01483937SEMDUpdated Jun 27, 2014Results posted

Evaluation of a Sensory Enrichment Multimodal Device (SEMD) on Physical Therapy Patients With Disequilibrium

An interventional study of Usual care physical therapy plus SEMD and Usual care physical therapy only in Vestibular Diseases, Labyrinth Diseases and Ear Diseases, sponsored by Karen L Atkins. Completed at 4 sites in United States. Open to participants aged 21 Years to 84 Years. Per ClinicalTrials.gov, last updated 2014-06-27.

Sponsored by Karen L Atkins · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
32
Allocation
Randomized
Ages
21 Years to 84 Years
Sex
All
01

Study summary

Purpose of this study is to determine the efficiency and safety of a Sensory Enrichment Multimodal Device (SEMD) when applied in conjunction with usual care vestibular-balance physical therapy for rehabilitation of patients who fall as a result of vestibular inducted disequilibrium.

Study participants will receive regular physical therapy, and some will use the SEMD device while receiving usual care vestibular-balance physical therapy. The device is an elastic belt that holds eight small battery powered vibrating disks. When using the device, you will sit or stand on a force platform that measures body sway. That movement information is sent to a computer which then sends the information to you via the vibrating disks. The vibrating disks are similar to a vibrating cell phone: you can feel the vibration but it is not uncomfortable. You can also see your sway movement on the computer screen. Some tests and activities will be paced with a beeping sound.

The aim of this study is six-fold: 1. Demonstrate the relative efficiency between SEMD and conventional vestibular-balance physical therapy as reported by treating physical therapists' by counting number of skills acquired in a treatment session, and the amount of time needed to acquire the skill; 2. Demonstrate greater improvement earlier on in balance test scores when using the SEMD as an adjunct to conventional vestibular-balance physical therapy; 3. Determine the difference in vestibular habituation between physical therapy plus SEMD and conventional vestibular-balance physical therapy; 4. Demonstrate a more immediate reduction in fall occurrence when using SEMD as an adjunct to conventional vestibular-balance physical therapy; 5. Determine the patient's perception of quality of life between physical therapy plus SEMD and conventional vestibular-balance physical therapy; 6. Determine difference in acquisition of large movement tasks of tandem walk, step quick-turn, and kneel-shoulder rifle-return to stand between subjects that have trained with SEMD and conventional vestibular-balance physical therapy .

In addition to primary and secondary outcome measurements, efficiency of skill acquisition, devised for this study, will be evaluated by tracking the number of skills and length of time needed to acquire each skill for each physical therapy session using the Patient Skill Acquisition Chart (PSAC). Usefulness of Tandem Walk, Step Quick-turn, and Kneel- Shoulder Rifle-Return to Stand as intervention outcome, also devised for this study, will be evaluated with pre test to post tests Modified Functional Independence Measure - Motor (MFIM-Motor). These measurements were devised for this study, and will be evaluated for informational purposes only.

Read the detailed description

This study will compare two approaches of physical therapy intervention within vestibular deficit populations that frequently fall: 1. physical therapy plus SEMD, and 2. usual care physical therapy only.

Multimodal sensory cueing gives additional or enriched information to complement postural and mobility decisions. SEMD displays combine vibrotactile, visual and audio cueing that are intuitive and non-intrusive within a balance training system.

Study intervention includes a maximum of 12 physical therapy intervention sessions, 2 times per week for 6 weeks or normalization of SOT, whichever occurs first. Usual care physical therapy prescriptions are written specific for number of sessions over a specific duration of time. Discharge from physical therapy occurs when number of sessions within a specified period of time is exhausted or goals specified by the physical therapist are met. Data collection includes 1 pre test and 4 post tests at intervals during the weeks of intervention, plus 3 follow-up phone interviews at specified intervals after intervention for maximal study duration of 6 months. A patient must attend at least 4 physical therapy intervention sessions for their data to be used and for the follow-up phone interviews to be initiated.

02

Conditions studied

  • Vestibular Diseases
  • Labyrinth Diseases
  • Ear Diseases
  • Otorhinolaryngologic Diseases
  • Traumatic Brain Injury

Keywords

  • Keywords provided by BalanceSense, LLC:
  • Physical Therapy
  • Rehabilitation
  • Disequilibrium
  • Balance dysfunction or disorder
  • Vestibular
  • Mild Traumatic Brain Injury (mTBI)
  • Vibrotactile
03

In context

Vestibular Diseases

170 studies on the registry are indexed under Vestibular Diseases; 41 are open to participants now.

This study's enrollment of 32 is below the median of 46 across 127 interventional studies indexed under Vestibular Diseases.

Browse Vestibular Diseases studies →

Lead sponsor

This is the only study on the registry with Karen L Atkins as lead sponsor.

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

04

Who can participate

Ages eligible
21 Years to 84 Years
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

  1. Self-reporting 2 or more falls with or without injury within the past 6 months.
  2. Below normal SOT containing a abnormal vestibular score.
  3. Potential to benefit from physical therapy as indicated by physician prescription referral.
  4. Able to sit and to stand unaided for 2 minutes.
  5. Willing and able to complete all testing, training, and follow-up evaluations required by the study protocol.

Exclusion criteria

Exclusion Criteria:

  1. Fluctuating Meniere's
  2. Vestibular injury requiring surgery such as perilymph fistula
  3. Moderate progressive neurologic disease such as multiple sclerosis
  4. Does not speak and understand the English language
  5. Resides in a nursing home
  6. Unable to provide own consent.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
32 participants (actual)

Study arms

  • Active comparator
    Usual care physical therapy only

    Subjects will receive usual care physical therapy intervention provided by vestibular and balance specialists. Usual care physical therapy, in general, includes but is not limited to static and dynamic balance activities with or without head movements on firm floor or compliant surfaces.

    Other: Usual care physical therapy only

  • Experimental
    Usual care physical therapy plus SEMD

    Subjects will receive usual care physical therapy intervention provided by vestibular balance specialists while using the Sensory Enrichment Multimodal Device (SEMD). SEMD protocols use visual, vibrotactile, and auditory cueing referenced to subject's Center of Gravity (COG) and/or Sum of Pressure (SOP) data collected from a force platform upon which the subject is placed. Static and dynamic balance activities with or without head movement are preformed while watching a computer screen; paced with an auditory metronome; and cued by "touch" vibration via coin tactors imbedded in a belt worn around the waist matching the COG/SOP data display.

    Device: Usual care physical therapy plus SEMD

Interventions

  • DeviceUsual care physical therapy plus SEMD

    Patients will receive usual care physical therapy while wearing SEMD. SEMD protocols will also be provided to device subjects.

    Also known as: BalanceSense

  • OtherUsual care physical therapy only

    Subjects will receive usual care physical therapy from vestibular and balance specialists.

06

What researchers measure

Primary outcomes

  1. Assessment of the Efficacy of the SEMD Device in Improving Vestibular Function Was Evaluated With Change in Pre Test to Post Test 1 Sensory Organization Test (SOT).

    Sensory Organization Test (SOT) is a standing balance test that measures the subject's ability to control postural sway under vestibular, visual, and somatosensory conflict. Score ranges from 0 to 100 with higher score indicating better control of postural sway.

    Time frame: Pre Test to Post Test 1 after two physical therapy sessions (one week)

  2. Assessment of the Efficacy of the SEMD Device in Improving Vestibular Function Was Evaluated With Change in Post Test 1 to Post Test 2 Sensory Organization Test (SOT).

    Sensory Organization Test (SOT) is a standing balance test that measures the subject's ability to control postural sway under vestibular, visual, and somatosensory conflict. Score ranges from 0 to 100 with higher score indicating better control of postural sway.

    Time frame: Post Test 1 to Post Test 2 after four physical therapy sessions (two weeks)

  3. Assessment of the Efficacy of the SEMD Device in Improving Vestibular Function Was Evaluated With Change in Post Test 2 to Post Test 3 Sensory Organization Test (SOT).

    Sensory Organization Test (SOT) is a standing balance test that measures the subject's ability to control postural sway under vestibular, visual, and somatosensory conflict. Score ranges from 0 to 100 with higher score indicating better control of postural sway.

    Time frame: Post Test 2 to Post Test 3 after eight physical therapy sessions (4 weeks)

  4. Assessment of the Efficacy of the SEMD Device in Improving Vestibular Function Was Evaluated With Change From Post Test 3 to Post Test 4 Sensory Organization Test (SOT).

    Sensory Organization Test (SOT) is a standing balance test that measures the subject's ability to control postural sway under vestibular, visual, and somatosensory conflict. Score ranges from 0 to 100 with higher score indicating better control of postural sway.

    Time frame: Post Test 3 to Post Test 4 after twelve physical therapy sessions (6 weeks)

Secondary outcomes

  1. Percent of Subjects Decreasing Fall Risk Measured by Functional Gait Assessment Pre Test to Post Test 2

    Functional Gait Assessment is a 10-item gait assessment based on the Dynamic Gait Index. Requirements: A marked 20 foot walkway that is marked with a 12 inch width. Scoring: a four-point ordinal scale, ranging from 0-3 where "0" indicates the lowest level of function and "3" the highest level of function. Total Score = 30 with higher score indicating safer ambulation with lower risk of falling. Criterion Validity: "Authors support a cut off score of 23/30 for independent safe ambulation". Interpretation: 1) 0-19 is predictive of falls in the elderly. 2) 20-22 indicates likelihood of unexplained fall in community-dwelling, older adults, and predictive of likelihood of falling in patients with vestibular disorders. 3) 23-30 = safe ambulators

    Time frame: Pre Test to Post Test 2 after four physical therapy sessions within 10 days

  2. Percent of Subjects Reporting Decrease in Self-report Fall(s) Occurrence Pre Test to Post Test 1

    A fall is an unintentional change in position causing an individual to land at a lower level, on an object, the floor, the ground or other surface with or without injury. This includes: slips, trips, falling into other people, being lowered, loss of balance, and legs giving way. (Exclude sudden onset of paralysis, epileptic seizure, or overwhelming external force.)

    Time frame: Pre Test to Post Test 1 after 2 physical therapy sessions within 4 days

  3. Percent of Subjects Decreasing Fall Risk Measured by Berg Balance Scale Pre Test to Post Test 2

    Berg Balance Scale Description: 14-item scale designed to measure balance of the older adult in a clinical setting, and measures mobility related to activities of daily living. Description: This 14-item performance-based instrument is intended for individuals with some degree of balance impairment. Scoring: A five-point ordinal scale, ranging from 0-4. "0" indicates the lowest level of function and "4" the highest level of function. Total Score = 56 with higher score indicting safer ambulation with lower risk of falling. Criterion Validity: "Authors support a cut off score of 45/56 for independent safe ambulation". Interpretation: 41-56 = low fall risk 21-40 = medium fall risk 0 -20 = high fall risk Riddle and Stratford, 1999, examined 45/56 cutoff validity and concluded: * Sensitivity = 64% (Correctly predicts fallers) * Specificity = 90% (Correctly predicts non-fallers)

    Time frame: Pre Test, Post Test 2 after 4 physical therapy sessions within 10 days.

  4. Self-rated Disability Measured by Vestibular Rehabilitation Benefit Questionnaire Pre Test to Post Test 4

    Vestibular Rehabilitation Benefit Questionnaire asks the patient to self-rate disability as it affects their quality of life. Scale goes from zero, no disability, to 100 or maximal disability. The Total Benefit includes two subsets: 1) dizziness symptoms, and 2) quality of life.

    Time frame: Pre test to Post Test 4 or 12 Physical Therapy sessions within 42 days

  5. Head Shake Sensory Organization Test (HS_SOT)

    Head Shake Sensory Organization Test (HS-SOT) HS-SOT instructs the patient to static stand shoulder width apart with eyes closed and uses the SOT Condition 5 sway surface protocol while shaking the head horizontally 120 degrees per second. This protocol is safe for patients when they have normalized all SOT scores. Because study subjects were reaching SOT normalization after Post Test 2, the data collected was scant and not suitable for analysis.

    Time frame: Pre Test, Post Test 1 and Post Test 4

07

Results

Posted Jun 27, 2014
Limitations and caveats
Small number of subjects recruited because of lengthy study commitment.

Participant flow

Recruitment continued for one year resulting in 39 subjects pre screened for inclusion in the study.

Participant flow — Overall Study
MilestoneConventional Care Physical Therapy OnlyConventional Physical Therapy Plus SEMD
Started1517
Completed1114
Not completed43
Withdrew: Withdrawal by subject43

Outcome measures

PrimaryAssessment of the Efficacy of the SEMD Device in Improving Vestibular Function Was Evaluated With Change in Pre Test to Post Test 1 Sensory Organization Test (SOT).

Sensory Organization Test (SOT) is a standing balance test that measures the subject's ability to control postural sway under vestibular, visual, and somatosensory conflict. Score ranges from 0 to 100 with higher score indicating better control of postural sway.

Time frame:
Pre Test to Post Test 1 after two physical therapy sessions (one week)
Reported as:
Mean · units on a scale
Assessment of the Efficacy of the SEMD Device in Improving Vestibular Function Was Evaluated With Change in Pre Test to Post Test 1 Sensory Organization Test (SOT).
units on a scaleConventional Care Physical Therapy OnlyConventional Physical Therapy Plus SEMD
Assessment of the Efficacy of the SEMD Device in Improving Vestibular Function Was Evaluated With Change in Pre Test to Post Test 1 Sensory Organization Test (SOT).9.82 ± 10.687.29 ± 9.33
Statistical analysis
  • Conventional Care Physical Therapy Only vs Conventional Physical Therapy Plus SEMD · ANOVA · p = .533
PrimaryAssessment of the Efficacy of the SEMD Device in Improving Vestibular Function Was Evaluated With Change in Post Test 1 to Post Test 2 Sensory Organization Test (SOT).

Sensory Organization Test (SOT) is a standing balance test that measures the subject's ability to control postural sway under vestibular, visual, and somatosensory conflict. Score ranges from 0 to 100 with higher score indicating better control of postural sway.

Time frame:
Post Test 1 to Post Test 2 after four physical therapy sessions (two weeks)
Reported as:
Mean · units on a scale
Assessment of the Efficacy of the SEMD Device in Improving Vestibular Function Was Evaluated With Change in Post Test 1 to Post Test 2 Sensory Organization Test (SOT).
units on a scaleConventional Care Physical Therapy OnlyConventional Physical Therapy Plus SEMD
Assessment of the Efficacy of the SEMD Device in Improving Vestibular Function Was Evaluated With Change in Post Test 1 to Post Test 2 Sensory Organization Test (SOT).9.36 ± 12.805.00 ± 8.49
PrimaryAssessment of the Efficacy of the SEMD Device in Improving Vestibular Function Was Evaluated With Change in Post Test 2 to Post Test 3 Sensory Organization Test (SOT).

Sensory Organization Test (SOT) is a standing balance test that measures the subject's ability to control postural sway under vestibular, visual, and somatosensory conflict. Score ranges from 0 to 100 with higher score indicating better control of postural sway.

Time frame:
Post Test 2 to Post Test 3 after eight physical therapy sessions (4 weeks)
Reported as:
Mean · units on a scale
Assessment of the Efficacy of the SEMD Device in Improving Vestibular Function Was Evaluated With Change in Post Test 2 to Post Test 3 Sensory Organization Test (SOT).
units on a scaleConventional Care Physical Therapy OnlyConventional Physical Therapy Plus SEMD
Assessment of the Efficacy of the SEMD Device in Improving Vestibular Function Was Evaluated With Change in Post Test 2 to Post Test 3 Sensory Organization Test (SOT).3.27 ± 7.948.86 ± 7.72
PrimaryAssessment of the Efficacy of the SEMD Device in Improving Vestibular Function Was Evaluated With Change From Post Test 3 to Post Test 4 Sensory Organization Test (SOT).

Sensory Organization Test (SOT) is a standing balance test that measures the subject's ability to control postural sway under vestibular, visual, and somatosensory conflict. Score ranges from 0 to 100 with higher score indicating better control of postural sway.

Time frame:
Post Test 3 to Post Test 4 after twelve physical therapy sessions (6 weeks)
Reported as:
Mean · units on a scale
Assessment of the Efficacy of the SEMD Device in Improving Vestibular Function Was Evaluated With Change From Post Test 3 to Post Test 4 Sensory Organization Test (SOT).
units on a scaleConventional Care Physical Therapy OnlyConventional Physical Therapy Plus SEMD
Assessment of the Efficacy of the SEMD Device in Improving Vestibular Function Was Evaluated With Change From Post Test 3 to Post Test 4 Sensory Organization Test (SOT).5.09 ± 6.70.86 ± 6.57
SecondaryPercent of Subjects Decreasing Fall Risk Measured by Functional Gait Assessment Pre Test to Post Test 2

Functional Gait Assessment is a 10-item gait assessment based on the Dynamic Gait Index. Requirements: A marked 20 foot walkway that is marked with a 12 inch width. Scoring: a four-point ordinal scale, ranging from 0-3 where "0" indicates the lowest level of function and "3" the highest level of function. Total Score = 30 with higher score indicating safer ambulation with lower risk of falling. Criterion Validity: "Authors support a cut off score of 23/30 for independent safe ambulation". Interpretation: 1) 0-19 is predictive of falls in the elderly. 2) 20-22 indicates likelihood of unexplained fall in community-dwelling, older adults, and predictive of likelihood of falling in patients with vestibular disorders. 3) 23-30 = safe ambulators

Time frame:
Pre Test to Post Test 2 after four physical therapy sessions within 10 days
Reported as:
Number · percentage of participants
Percent of Subjects Decreasing Fall Risk Measured by Functional Gait Assessment Pre Test to Post Test 2
percentage of participantsConventional Care Physical Therapy OnlyConventional Physical Therapy Plus SEMD
Percent of Subjects Decreasing Fall Risk Measured by Functional Gait Assessment Pre Test to Post Test 220 ± 2.3877 ± 2.01
SecondaryPercent of Subjects Reporting Decrease in Self-report Fall(s) Occurrence Pre Test to Post Test 1

A fall is an unintentional change in position causing an individual to land at a lower level, on an object, the floor, the ground or other surface with or without injury. This includes: slips, trips, falling into other people, being lowered, loss of balance, and legs giving way. (Exclude sudden onset of paralysis, epileptic seizure, or overwhelming external force.)

Time frame:
Pre Test to Post Test 1 after 2 physical therapy sessions within 4 days
Reported as:
Number · percentage of participants
Percent of Subjects Reporting Decrease in Self-report Fall(s) Occurrence Pre Test to Post Test 1
percentage of participantsConventional Care Physical Therapy OnlyConventional Physical Therapy Plus SEMD
Percent of Subjects Reporting Decrease in Self-report Fall(s) Occurrence Pre Test to Post Test 1954
SecondaryPercent of Subjects Decreasing Fall Risk Measured by Berg Balance Scale Pre Test to Post Test 2

Berg Balance Scale Description: 14-item scale designed to measure balance of the older adult in a clinical setting, and measures mobility related to activities of daily living. Description: This 14-item performance-based instrument is intended for individuals with some degree of balance impairment. Scoring: A five-point ordinal scale, ranging from 0-4. "0" indicates the lowest level of function and "4" the highest level of function. Total Score = 56 with higher score indicting safer ambulation with lower risk of falling. Criterion Validity: "Authors support a cut off score of 45/56 for independent safe ambulation". Interpretation: 41-56 = low fall risk 21-40 = medium fall risk 0 -20 = high fall risk Riddle and Stratford, 1999, examined 45/56 cutoff validity and concluded: * Sensitivity = 64% (Correctly predicts fallers) * Specificity = 90% (Correctly predicts non-fallers)

Time frame:
Pre Test, Post Test 2 after 4 physical therapy sessions within 10 days.
Reported as:
Number · percentage of participants
Percent of Subjects Decreasing Fall Risk Measured by Berg Balance Scale Pre Test to Post Test 2
percentage of participantsConventional Care Physical Therapy OnlyConventional Physical Therapy Plus SEMD
Percent of Subjects Decreasing Fall Risk Measured by Berg Balance Scale Pre Test to Post Test 243100
SecondarySelf-rated Disability Measured by Vestibular Rehabilitation Benefit Questionnaire Pre Test to Post Test 4

Vestibular Rehabilitation Benefit Questionnaire asks the patient to self-rate disability as it affects their quality of life. Scale goes from zero, no disability, to 100 or maximal disability. The Total Benefit includes two subsets: 1) dizziness symptoms, and 2) quality of life.

Time frame:
Pre test to Post Test 4 or 12 Physical Therapy sessions within 42 days
Reported as:
Mean · units on a scale
Self-rated Disability Measured by Vestibular Rehabilitation Benefit Questionnaire Pre Test to Post Test 4
units on a scaleConventional Care Physical Therapy OnlyConventional Physical Therapy Plus SEMD
Pre Test39.14 ± 17.9534.30 ± 6.52
Post Test 431.27 ± 8.2528.32 ± 11.10
SecondaryHead Shake Sensory Organization Test (HS_SOT)

Head Shake Sensory Organization Test (HS-SOT) HS-SOT instructs the patient to static stand shoulder width apart with eyes closed and uses the SOT Condition 5 sway surface protocol while shaking the head horizontally 120 degrees per second. This protocol is safe for patients when they have normalized all SOT scores. Because study subjects were reaching SOT normalization after Post Test 2, the data collected was scant and not suitable for analysis.

Time frame:
Pre Test, Post Test 1 and Post Test 4

No measurements were reported for this outcome.

Adverse events

Collected over 1 year. Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Conventional Care Physical Therapy Only—0/15 (0%)0/15 (0%)
Conventional Physical Therapy Plus SEMD—0/17 (0%)0/17 (0%)

Baseline characteristics

4 withdrew from Conventional care physical therapy 3 withdrew from Conventional care physical therapy plus SEMD

Age, Categorical
Age, Categorical(Participants)Conventional Care Physical Therapy OnlyConventional Physical Therapy Plus SEMDTotal
<=18 years000
Between 18 and 65 years314
>=65 years81321
Age, Continuous
Age, Continuous(years)Conventional Care Physical Therapy OnlyConventional Physical Therapy Plus SEMDTotal
Mean69.44 ± 10.0073.35 ± 7.4671.64 ± 8.70
Sex: Female, Male
Sex: Female, Male(Participants)Conventional Care Physical Therapy OnlyConventional Physical Therapy Plus SEMDTotal
Female71017
Male448
Region of Enrollment
Region of Enrollment(participants)Conventional Care Physical Therapy OnlyConventional Physical Therapy Plus SEMDTotal
United States111425
08

Study locations

4 sites
  • England Physical Therapy
    Garden Grove, California 92840, United States
  • Florida Ear & Balance Center
    Celebration, Florida 34747, United States
  • Stevenson & Associates Physical Therapy
    Fort Myers, Florida 33908, United States
  • Brooks Balance Center
    Jacksonville, Florida 32216, United States
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 27, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT01483937
Lead sponsor
Karen L Atkins
Responsible party
Karen L Atkins (Study Director, BalanceSense LLC) — Sponsor-investigator
First posted
Dec 2, 2011
Start date
Nov 2011
Primary completion
May 2013
Completion
Aug 2013
Results posted
Jun 27, 2014
Last update
Jun 27, 2014

Study contacts

Karen L Atkins, PhD, PT
study director · BalanceSense LLC

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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