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Balance Rehabilitation With Sensory Recalibration After Stroke (AVCPOSTIM)

Primary Purpose

Left-sided Hemiplegia Affecting Dominant Side as Late Effect of Cerebrovascular Accident

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Cervical vibration
Prism adaptation
Conventional rehabilitation
Sponsored by
Rennes University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Left-sided Hemiplegia Affecting Dominant Side as Late Effect of Cerebrovascular Accident focused on measuring Balance,Hemiplegia,Cervical vibration,Prism adaptation,Rehabilitation

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Right unilateral supratentorial ischemic or hemorrhagic lesion
  • Adult (age ≥ 18 years) under 80 years
  • Stroke

    • older than 9 months
    • with or without hemianopsia
    • with or without visuospatial hemineglect
  • The first symptomatic episode
  • Standing balance ≥ 30 sec unaided
  • Percentage of weight rests on the hemiplegic lower limb below 40% of body weight (on a platform of strength)
  • Written informed consent of the patient or a member of his entourage (in the case of patients with motor difficulties)

Exclusion Criteria:

  • Orthopedic, rheumatologic or visual disorders affecting the distribution of the center of pressure while standing
  • Visual disorder that does not allow assessment of the longitudinal axis or visual straight ahead
  • Ischemic or hemorrhagic brain stem lesion
  • Trouble for understanding protocol procedures

Inclusion Criteria for the healthy volunteers (ancillary study) :

  • Age ≥ 18 years, right-handed, sex and age-matched (+/- 5 years) to the patients of the coordinating center
  • Able to get an MRI
  • With no imbalance
  • With no visual disorder impacting the repartition of the center of pression when standing up, or that does not allow assessment of the longitudinal axis or visual straight ahead
  • Written informed consent

Sites / Locations

  • CHU Grenoble
  • CHU Lille
  • CHU Lyon
  • IRF Nancy
  • CHU Lariboisière-Saint Louis Paris
  • Centre de Rééducation de Kerpape
  • CHU Reims
  • CHU Rennes-Pontchaillou

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Experimental

Experimental

Experimental

Arm Label

Control group

Cervical vibration

Prism adaptation

Cervical vibration + Prism adaptation

Arm Description

This group will benefit from conventional rehabilitation

This group will benefit from a daily 20 minutes session, with vibration of neck muscles during 10 minutes

This group will benefit from a daily 20 minutes session, with prism adaptation during 10 minutes

This group will receive a daily 30 minutes session, with cervical vibration during 10 minutes + prism adaptation during 10 minutes

Outcomes

Primary Outcome Measures

The primary outcome is the deviation of the mean position of center of pressure (CP) (eyes closed) on the mediolateral axis (mm) assessed by posturography after intervention.

Secondary Outcome Measures

Evaluation of balance
Postural Assessment Scale for Stroke Scale for Contraversive Pushing Berg Balance Scale Timed Up and Go Measurement performed on the platform of strength: surface of the center of mass displacement deviation of the mean position of the center pressure on the anteroposterior axis standard deviation of the average displacement of the center pressure on the mediolateral axis and the anteroposterior axis, percentage of support on the hemiplegic lower limb.
Evaluation of functional capacity
Barthel Index (Day 0, Day 14, Month 3, Month 6) Number of hours of help at home (Month 3, Month 6) Total Duration of hospitalization since the Cerebral Vascular Accident (Month 3, Month 6)
Evaluation of negligence
Bell test, Bisection test, Scale of Catherine Bergego, OTA test Test of bodily neglect.
Understanding the mechanisms of sensory manipulations
Evaluation of longitudinal axis by a fluorescent bar movement in front of the patient through a computerized system. Haptic Straight Ahead using a graduated table on which the subject moves his hand blindfolded.

Full Information

First Posted
August 29, 2012
Last Updated
May 22, 2023
Sponsor
Rennes University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01677091
Brief Title
Balance Rehabilitation With Sensory Recalibration After Stroke
Acronym
AVCPOSTIM
Official Title
Effectiveness of a Balance Rehabilitation Program With Sensory Recalibration After Stroke: A Randomized Controlled Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Completed
Study Start Date
May 5, 2013 (Actual)
Primary Completion Date
October 14, 2019 (Actual)
Study Completion Date
October 14, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Rennes University Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The main objective of this study is to test the effectiveness of a rehabilitation program with cervical vibration and/or prism adaptation in patients with left hemiplegia on balance.
Detailed Description
Imbalance is particularly severe after a Cerebral Vascular Accident because they not only limit the capacity of transfer and are a source of falls but also represent an obstacle to the acquisition of autonomy. When the brain lesion is located in the right hemisphere, the prognosis in terms of equilibrium is worse probably because of the presence of disorders of spatial cognition. These disorders of spatial cognition are manifested by a distortion of the mental representation of space and body in space that probably cause a deviation of the position of the center of pression on platform. This component of balance disorders secondary to disruption of spatial cognition, do not benefit at present from specific rehabilitative treatment despite the severity of the consequences. But the application of sensory manipulations has proven its effectiveness on visuospatial neglect that is another disorder of spatial cognition closed to the pathophysiology of balance disorders after right brain lesion. Sensory manipulations decrease the distortion of internal representations of the body in space by restoring the symmetry of sensory inputs. Some of these manipulations (visual manipulation by wearing prisms and proprioceptive manipulations) are also effective on the immediate correction of postural imbalances on force platform and disorders of spatial perception. We therefore believe that the approach by repeated sensory manipulation is a new promising way of research for the rehabilitative treatment of balance disorders secondary to disorders of spatial cognition. As the mechanisms of action and the structures involved during proprioceptive vibration of neck muscles and during visual prism adaptation are different, we believe that the combination of these two types of sensory manipulations will permit to obtain a greater and longer lasting effect than a lonely manipulation. The concomitant evaluation of the bias on postural platform and the perception of the body axis will allow us to assess the impact of such rehabilitation on the disorders of spatial representation and so better understand the mechanisms of action of sensory manipulations. The main objective of this study is to test the effectiveness of a rehabilitation program with cervical vibration (V) and / or prism adaptation (P) in patients with left hemiplegia on balance at the end of the intervention (day14). Secondary objectives are to test: The immediate effect (day 0) on force platform evaluation of balance, Maintaining the gain at 3 months and 6 months on balance, Effectiveness at day 14 on negligence Maintaining the gain at 3 months and 6 months on neglect, Effectiveness at day 14 on functional abilities, Maintaining the gain at 3 months and 6 months on functional abilities, Understanding the mechanisms of action of each of the sensory manipulations by assessing changes in perceptions of space, after rehabilitation programs (day 14) and at 3 months and 6 months. To evaluate the evolution of motility, sensitivity and spasticity in the various assessments. During the 15 days rehabilitation performed for the study, the upper and lower limbs motor rehabilitation will last less than one hour and a half, and will exclude instrumental techniques of balance rehabilitation, sensory manipulations, virtual reality, strain-induced therapy. Moreover, an ancillary study will be performed to study the immediate neurofunctional effect of vibratory stimulation, in right brain-damaged patients with imbalance and in healthy volunteers, through the assessment of cerebral activation changes in MRI. The secondary objectives of this ancillary study are to test the neurofunctional effect of repeated vibratory stimulation in right brain-damaged patients, describe the relationship between cerebral activation changes and evolution of balance, and describe the areas of the brain activated by vibratory stimulation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Left-sided Hemiplegia Affecting Dominant Side as Late Effect of Cerebrovascular Accident
Keywords
Balance,Hemiplegia,Cervical vibration,Prism adaptation,Rehabilitation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
114 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control group
Arm Type
Active Comparator
Arm Description
This group will benefit from conventional rehabilitation
Arm Title
Cervical vibration
Arm Type
Experimental
Arm Description
This group will benefit from a daily 20 minutes session, with vibration of neck muscles during 10 minutes
Arm Title
Prism adaptation
Arm Type
Experimental
Arm Description
This group will benefit from a daily 20 minutes session, with prism adaptation during 10 minutes
Arm Title
Cervical vibration + Prism adaptation
Arm Type
Experimental
Arm Description
This group will receive a daily 30 minutes session, with cervical vibration during 10 minutes + prism adaptation during 10 minutes
Intervention Type
Other
Intervention Name(s)
Cervical vibration
Intervention Description
Vibration of neck muscles during 10 minutes
Intervention Type
Other
Intervention Name(s)
Prism adaptation
Intervention Description
Prism adaptation during 10 minutes
Intervention Type
Other
Intervention Name(s)
Conventional rehabilitation
Intervention Description
conventional rehabilitation
Primary Outcome Measure Information:
Title
The primary outcome is the deviation of the mean position of center of pressure (CP) (eyes closed) on the mediolateral axis (mm) assessed by posturography after intervention.
Time Frame
Day 14
Secondary Outcome Measure Information:
Title
Evaluation of balance
Description
Postural Assessment Scale for Stroke Scale for Contraversive Pushing Berg Balance Scale Timed Up and Go Measurement performed on the platform of strength: surface of the center of mass displacement deviation of the mean position of the center pressure on the anteroposterior axis standard deviation of the average displacement of the center pressure on the mediolateral axis and the anteroposterior axis, percentage of support on the hemiplegic lower limb.
Time Frame
Day 0, Day 14, Month 3, Month 6
Title
Evaluation of functional capacity
Description
Barthel Index (Day 0, Day 14, Month 3, Month 6) Number of hours of help at home (Month 3, Month 6) Total Duration of hospitalization since the Cerebral Vascular Accident (Month 3, Month 6)
Time Frame
Day 0, Day 14, Month 3, Month 6
Title
Evaluation of negligence
Description
Bell test, Bisection test, Scale of Catherine Bergego, OTA test Test of bodily neglect.
Time Frame
Day 0, Day 14, Month 3, Month 6
Title
Understanding the mechanisms of sensory manipulations
Description
Evaluation of longitudinal axis by a fluorescent bar movement in front of the patient through a computerized system. Haptic Straight Ahead using a graduated table on which the subject moves his hand blindfolded.
Time Frame
Day 0, Day 14, Month 3, Month 6
Other Pre-specified Outcome Measures:
Title
Time since stroke
Time Frame
day 0
Title
Extent of the injury and localization of brain injury
Description
Assessed by morphological MRI with DT1, TSE T2 and flair sequences, to achieve a morphological analysis of the lesion. The MRI will be read back by Rennes.
Time Frame
>2 months after hemiplegia
Title
Severity of hemiplegia
Description
motility index, Barthel
Time Frame
day 0
Title
Study the effect of vibratory stimulation by studying changes in brain activity in particular areas of interest involved in the representation of the body (ancillary study)
Description
Day 0 : Functional MRI analysis for the patients included in the coordinating center (Rennes). Week 3 : Among these patients, a second functional MRI will be performed for the first 10 patients of the cervical vibration group and first 10 patients of the conventional rehabilitation group, and for 20 age and sex-matched healthy volunteers.
Time Frame
Day 0, Week 3

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Right unilateral supratentorial ischemic or hemorrhagic lesion Adult (age ≥ 18 years) under 80 years Stroke older than 9 months with or without hemianopsia with or without visuospatial hemineglect The first symptomatic episode Standing balance ≥ 30 sec unaided Percentage of weight rests on the hemiplegic lower limb below 40% of body weight (on a platform of strength) Written informed consent of the patient or a member of his entourage (in the case of patients with motor difficulties) Exclusion Criteria: Orthopedic, rheumatologic or visual disorders affecting the distribution of the center of pressure while standing Visual disorder that does not allow assessment of the longitudinal axis or visual straight ahead Ischemic or hemorrhagic brain stem lesion Trouble for understanding protocol procedures Inclusion Criteria for the healthy volunteers (ancillary study) : Age ≥ 18 years, right-handed, sex and age-matched (+/- 5 years) to the patients of the coordinating center Able to get an MRI With no imbalance With no visual disorder impacting the repartition of the center of pression when standing up, or that does not allow assessment of the longitudinal axis or visual straight ahead Written informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Isabelle BONAN, PU PH
Organizational Affiliation
Rennes University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU Grenoble
City
Grenoble
ZIP/Postal Code
38701
Country
France
Facility Name
CHU Lille
City
Lille
ZIP/Postal Code
59000
Country
France
Facility Name
CHU Lyon
City
Lyon
Country
France
Facility Name
IRF Nancy
City
Nancy
Country
France
Facility Name
CHU Lariboisière-Saint Louis Paris
City
Paris
ZIP/Postal Code
75010
Country
France
Facility Name
Centre de Rééducation de Kerpape
City
Ploemeur
ZIP/Postal Code
56270
Country
France
Facility Name
CHU Reims
City
Reims
ZIP/Postal Code
51100
Country
France
Facility Name
CHU Rennes-Pontchaillou
City
Rennes
ZIP/Postal Code
35000
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
34439582
Citation
Leplaideur S, Moulinet-Raillon A, Duche Q, Chochina L, Jamal K, Ferre JC, Bannier E, Bonan I. The Neural Bases of Egocentric Spatial Representation for Extracorporeal and Corporeal Tasks: An fMRI Study. Brain Sci. 2021 Jul 22;11(8):963. doi: 10.3390/brainsci11080963.
Results Reference
result
PubMed Identifier
32245547
Citation
Jamal K, Leplaideur S, Rousseau C, Cordillet S, Raillon AM, Butet S, Cretual A, Bonan I. The effects of repetitive neck-muscle vibration on postural disturbances after a chronic stroke. Neurophysiol Clin. 2020 Sep;50(4):269-278. doi: 10.1016/j.neucli.2020.01.005. Epub 2020 Mar 31.
Results Reference
result

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Balance Rehabilitation With Sensory Recalibration After Stroke

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