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SWAY Mobile Application Assessments in Healthy Adults

NCT05616975 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2024-03-29

No results posted yet for this study

Summary

SWAY Medical, Inc. (SWAY) has developed a mobile application that assesses balance, functional performance, and cognitive function. Clinical reliability, validity, and normative data have been studied extensively in individuals aged 5 to 20. The accuracy of the SWAY Mobile Application in assessing conditions associated with head injury has also been well established. The objectives of this study are to examine the reliability and validity, and establish normative data, for SWAY balance, functional, and cognitive assessments in healthy adults aged 21-90. The SWAY smartphone app will be used to record balance, simple reaction time, impulse control, inspection time, working memory, reverse number counting, flanker task, modified Stroop, and 30 second chair stand test results. The following tests will be administered to participants: Test of Premorbid Functioning, WAIS-IV Logical Memory, WMS-IV Older Adult Logical Memory, Animal Fluency, Boston Naming Test, D-KEFS Color Word Interference Test, WMS-IV Symbol Span, WAIS-IV Coding, Auditory Consonant Trigrams, Verbal Fluency (FAS), and Flanker Inhibitory Control and Attention Test.

Conditions

  • Reliability
  • Validity
  • Normative Data

Interventions

OTHER

test-retest reliability

Assessing the test-retest reliability of SWAY Balance, Functional, and Cognitive tests.

OTHER

construct validity

Investigating the construct validity of SWAY Balance, Functional, and Cognitive tests.

OTHER

normative data

Collection of normative SWAY Balance, Functional, and Cognitive data.

Sponsors & Collaborators

  • SWAY Medical, Inc

    collaborator UNKNOWN

  • College of Medicine Alumni Association

    collaborator UNKNOWN

  • Harvard Medical School (HMS and HSDM)

    collaborator OTHER

  • University of Oklahoma

    lead OTHER

Eligibility

Min Age
21 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-01-01
Primary Completion
2023-04-27
Completion
2023-04-27
FDA Device
Yes

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05616975 on ClinicalTrials.gov