NCT02350556

Brief Summary

For several years, the postural disorders assessment in hemiplegic patients was conducted through force plate, using the center of plantar pressure displacement in a static position. These are widely used in physical therapy both for assessment and rehabilitation of patients with balance disorders. For hemiplegic patients, an asymmetric distribution support on each foot and an increased surface area of postural sways (more marked on the medio lateral axis) are observed. These studies, based on the study of plantar pressure ,are not enough to providea full description of the spatio-temporal organization of postural components in hemiplegic patients. Indeed, postural stabilometric evaluation is based on a simplification of the human skeleton by considering it as a simple inverted pendulum swinging on his ankles. This simplified model can't be used in dynamic assessment because of the simultaneous contributions of several joints during movement. This restricts its clinical interest because patients are more exposed to imbalances and falls in dynamic situations. Thus, the hip angular movement results in a center plantar pressure displacementwhich is impossible to discriminate from the ankle axis movement using stabilometric signal only. Thus, it seemed interesting to study another variable valid in dynamic conditions : the displacement of center of mass during a dynamic balancing task. This variable is obtained through 3D motion capture of the different segments of the human body. The dynamic test is a dynamic postural assessment following ball avoidance from three different directions. The center of mass displacement will be compared with a functional test known to be representative of dynamic balance of the individual capacities: The Timed Up and Go test (TUG). All of this data aims to improve the hemiplegic postural assessment for physical therapy and to help develop new rehabilitative approaches.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
63

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Mar 2015

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 26, 2015

Completed
3 days until next milestone

First Posted

Study publicly available on registry

January 29, 2015

Completed
1 month until next milestone

Study Start

First participant enrolled

March 9, 2015

Completed
1.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 3, 2016

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

November 23, 2016

Completed
Last Updated

May 31, 2017

Status Verified

May 1, 2017

Enrollment Period

1.2 years

First QC Date

January 26, 2015

Last Update Submit

May 29, 2017

Conditions

Outcome Measures

Primary Outcomes (1)

  • The primary outcome is the lateral displacement of the center of mass (CoM) in the frontal plane, obtained after recording the 3D motion using an optoelectronic device

    dynamic avoidance test in 7 days

Secondary Outcomes (4)

  • - to the functional level and the balance obtained from the test: Timed Up and Go test (TUG). This comparison will be made regarding the completion time of the test and the functional score in the Get Up and Go test.

    inclusion (0)

  • - using dynamic assessments : Maximum front displacement of the Plantar pressure center (CP) resultant when avoiding the central ball,

    dynamic avoidance test in 7 days

  • - Using static assessments : Postural asymmetry obtained by calculating the percentage of body weight distribution on each leg during the static postural initial assessment on force plate

    Inclusion (0)

  • The ABS TUG score (being validated) will also be compared to the lateral displacement of the center of mass (CoM).

    inclusio (0)

Study Arms (2)

hemiplegic patients

OTHER

Dynamic Avoidance Task

Other: Dynamic Avoidance TaskProcedure: physical therapyDevice: 3D motion on optoelectronic device

healthy volunteers

OTHER

Dynamic Avoidance Task

Other: Dynamic Avoidance TaskProcedure: physical therapyDevice: 3D motion on optoelectronic device

Interventions

healthy volunteershemiplegic patients
healthy volunteershemiplegic patients
healthy volunteershemiplegic patients

Eligibility Criteria

Age18 Years - 85 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • For hemiplegic patients:
  • Aged between 18-80 years of age, men and women
  • Left or right hemispheric sustentoriel stroke :
  • oIschemic or hemorragic oFirst symptomatic episode or TIA without consequences oBetween one month and one year since the stroke
  • Balance standing \> 30 sec without assistance in closed eyes condition
  • FAC score included between 3 and 7
  • Triceps Spasticity strictly less than 3 on the Modified Ashworth Scale with heel on the ground and an adductor spasticity up to 3 on the same scale.
  • Free, informed and written consent signed by the investigator and by the patient or one of his/her relatives (in the case of a patient able to understand the information and to express his/her consent but with motor difficulties resulting in the inability to sign)
  • For healthy volunteers :
  • Aged between 18-85 years of age, men or women, age-matched ( +/- 5 years ) with stroke patients
  • Without a balance disorder
  • Affiliated to social security
  • Free, informed and written consent

You may not qualify if:

  • For hemiplegic patients:
  • History of event affecting postural balance (orthopedic, rheumatological, neurological, ENT ...) before the stroke
  • Pregnant women
  • Patient with tiredness incompatible with the tests and instrumental assessments
  • Patients under legal protection (according to French law) and detainees.
  • Patients physically or mentally unable of giving informed consent
  • For healthy volunteers :
  • History of event affecting postural balance (orthopedic, rheumatological, neurological, ENT ...)
  • Receiving a psychotropic treatment (antidepressant, antipsychotic, anxiolytic)
  • Pregnant women
  • Patients under legal protection (according to French law) and detainees.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

CHU Rennes Pontchaillou

Rennes, 35000, France

Location

MeSH Terms

Interventions

Physical Therapy Modalities

Intervention Hierarchy (Ancestors)

TherapeuticsRehabilitation

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 26, 2015

First Posted

January 29, 2015

Study Start

March 9, 2015

Primary Completion

June 3, 2016

Study Completion

November 23, 2016

Last Updated

May 31, 2017

Record last verified: 2017-05

Locations