Skip to content

Is a low cost electronic measure of balance as valid as a force platform in distinguishing the balance performance of a healthy and a clinical older population?

Does a low cost electronic measure of balance classify balance performance as intact or impaired as accurately as a force platform in healthy and clinical older populations?

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12614000132640
Enrollment
40
Registered
2014-02-05
Start date
2014-04-23
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Do balance performance measures (both static and dynamic balance) on the low cost HUMAC Balance device have similar classification accuracy for balance impairment as the Neurocom EquiTest (Registered Trademark) System in healthy people over 60 years and people over 60 who have had a stroke

Interventions

This study seeks to determine concurrent validity of the CSMi HUMAC (Registered Trademark) Balance device against a ‘gold standard’ force platform measurement (Neurocom EquiTest (Registered Trademark) System). The 2 different devices will be used to assess balance in 2 populations: 1. a healthy group of community dwelling individuals aged >60 years (N=20); 2. a group of community dwelling individuals aged >60 who have had a stroke (subacute or chronic, ie > 6 weeks post stroke)(N=20). In a rando

This study seeks to determine concurrent validity of the CSMi HUMAC (Registered Trademark) Balance device against a ‘gold standard’ force platform measurement (Neurocom EquiTest (Registered Trademark) System). The 2 different devices will be used to assess balance in 2 populations: 1. a healthy group of community dwelling individuals aged >60 years (N=20); 2. a group of community dwelling individuals aged >60 who have had a stroke (subacute or chronic, ie > 6 weeks post stroke)(N=20). In a randomized order, subjects will undergo an assessment on each device over the course of about 1 hour. Assessment on the HUMAC device will include a modified Clinical Test of Sensory Interaction on Balance (mCTSIB) and a Limits of Stability (LOS) test. On the NeuroCom device a modified Sensory Organization Test (mSOT) and a LOS test will be performed. The mCTSIB and mSOT each have 4 conditions inwhich a subject stands still and has their balance assessed. The conditions include standing eyes open on a stable surface, standing eyes close on a stable surface, standing eyes open on a compliant surface, and standing eyes closed on a compliant surface. LOS testing requires subjects to stand still and then shift there weight as far as possible in 8 directions (N,NW,W,SW,S etc). Subjects will be given 3 minute rests between each test condition on either device as well as 5 minute rest when changing between devices.

Sponsors

Curtin University of Technology
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Primary purpose
Diagnosis

Eligibility

Sex/Gender
All
Age
60 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Healthy Population: >60 years, equal number of males and females, Community dwelling, can stand unsupported (no aids) for >1 min, walk >2 times/week, No falls history over prior 12 months Stroke Population: >60 years, equal number of males and females, sub-acute or chronic stroke (>6/52 previously), community dwelling, Able to stand unsupported for >1 min unaided.

Exclusion criteria

Healthy Population: Neurological or Musculoskeletal condition affecting balance

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026