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CompletedNCT05646966Updated Dec 12, 2022

Trunkstability: a Predisposition for Armfunction

An interventional study of one time testing in Trunk Stability, sponsored by University Ghent. Completed at 1 site in Belgium. Open to participants aged 18 Years to 70 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-12-12.

Sponsored by University Ghent · Not applicable, Interventional, and Basic science

From the registry’s dates

  • Registered 6 months after the study started (first participant enrolled Dec 2016, registered Jun 2017).
Phase
Not applicable
Study type
Interventional
Enrollment
110
Allocation
Non-randomized
Ages
18 Years to 70 Years
Sex
All
01

Study summary

Trunk stability is supposed to be an important predisposition for arm function. To the investors knowledge this is never been demonstrated.

Read the detailed description

Fifty healthy subjects will execute a reaching movement in sitting. They will reach to a cone at a distance of little more than armlength.

Electromyogram (EMG) and kinematics will be the outcome measures. Secondary outcome measures are: sex, dexterity, skillfulness, Fifty first time stroke patients will execute the same movements. Primery outcome is EMG and kinematics; secundary outcome measures are: side of hemiplegia, arm recuperation.

02

Conditions studied

  • Trunk Stability

Keywords

  • stroke
  • reaching
  • ADL
03

In context

Disease Susceptibility

141 studies on the registry are indexed under Disease Susceptibility; 31 are open to participants now.

This study's enrollment of 110 is below the median of 137 across 54 interventional studies indexed under Disease Susceptibility.

Browse Disease Susceptibility studies →

Lead sponsor

University Ghent is the lead sponsor of 345 studies on the registry; 85 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • BMI \< 30
  • no orthopedic, neurologic disorder that can influence the reaching
  • age between 18 and 70 yrs

Exclusion criteria

Exclusion Criteria:

  • BMI>30
  • orthopedic, neurologic disorder that can influence the reaching
  • \< 18 yrs of age
  • >70 yrs of age
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
110 participants (actual)

Study arms

  • Active comparator
    healthy subjects

    healthy subjects

    Other: one time testing

  • No intervention
    stroke patients

    first time stroke patients

Interventions

  • Otherone time testing
06

What researchers measure

Primary outcomes

  1. Electromyography to analyze muscle activation

    which muscle is active during a reaching movement

    Time frame: 2 hours

  2. kinematics to analyze trunk involvement

    when is the trunk involved in a reaching movement

    Time frame: 2 hours

07

Study locations

1 site
  • Revaki Ugent
    Gent, Oost Vlaanderen 9000, Belgium
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 12, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05646966
Lead sponsor
University Ghent
Collaborators
University Hospital, Ghent
Responsible party
Sponsor
First posted
Dec 12, 2022
Start date
Dec 2016
Primary completion
Jul 2019
Completion
Jul 2019
Last update
Dec 12, 2022

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2022. You cannot join it, but the record below documents what was studied.

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