Reliability, Validity and Clinical Utility of a Robotic Assessment of Finger Proprioception in Neurological Subjects

CompletedNot a drug-phase studyMS (type not specified)NCT03619642

What it found

No results found

We found no results in the registry or in papers.

This trial finished 8 years ago. We found no results in the registry or in any paper that cites it.

What was tested

Treatment tested

  • Robotic assessment of finger proprioception

What it measured

Main measures

  • Error

    day 2

  • Error

    day 3

Other measures (21)

  • sex

    day 1

  • Age

    day 1

  • medication use

    day 1

  • the modified Ashworth scale

    day 1

    Arm and hand functionSpasticity
  • Edinburgh Handedness Inventory

    day 1

  • Nine Hole Peg test

    day 1

    Arm and hand function
  • Box and block test

    day 1

    Arm and hand function
  • Manual Ability Measure-36 (questionnaire)

    day 1

    Arm and hand functionQuality of life (reported by participants)
  • Symbol digit modalities test

    day 1

    Thinking and memory
  • 25 foot walk test

    day 1

    Walking and mobility

Who could take part

MS (type not specified) · 18 and over

Show the full criteria

Inclusion criteria

Inclusion criteria MS subjects * Age > 18 years * Diagnosis of MS (McDonald criteria) * No relapse or relapse-related treatment within the last 3 months prior to the study Inclusion criteria Stroke subjects * Age > 18 years * Diagnosis of stroke (ischemic or hemorrhagic), * Between 2 weeks and 12 months post-stroke

Exclusion criteria

* Complete paralysis of both upper limbs * Unable to detect any passive movement in hand and fingers * Unable to place the hand in the robotic devices without any discomfort or pain * Marked or severe intention tremor (Fahn's tremor rating scale on finger-to-nose test > 3) * Marked or severe spasticity for finger and elbow flexors or shoulder adductors (Modified Asworth scale >3) * Other medical conditions interfering with the hand function (peripheral nerve lesion, orthopedic or rheumatoid impairment, pain, edema) * Severe cognitive or visual deficits interfering with testing and training (e.g. Aphasia, neglect, …)

As registered. Criteria can change, so ask the trial team or your neurologist.

About this trial

In the sponsor's words

The aim of this case-controlled observational cross-sectional study is to investigate the test-retest reliability, validity and clinical utility of a rapid robotic assessment of finger proprioception using a passive gauge position matching tasks in MS and stroke subjects. Session 1 Informed consent Descriptive measures Session 2 Clinical testing Robotic assessment (3x) Session 3 Clinical testing Robotic assessment (3x)

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History

    1. Started

      Dec 2017

    2. Main results due

      May 2018

    3. Finished

      May 2018

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