Vestibular Rehabilitation and Severe Traumatic Brain Injury

Sponsor
I.R.C.C.S. Fondazione Santa Lucia (Other)
Overall Status
Completed
CT.gov ID
NCT04415580
Collaborator
(none)
30
2
2
12.6
15
1.2

Study Details

Study Description

Brief Summary

Severe brain injury (sTBI) is one of the most common causes of long-term disability and is considered the most frequent cause of mortality and serious disability in young adults in industrialized countries. It is defined as an alteration of brain function with loss of consciousness in the acute phase for at least 24 hours (Glasgow Coma Scale (GCS) <8) and it can induce a wide range of deficit, including cognitive-behavioural, motors, psychics, language, vision, coordination and balance impairments. Chronic vestibular symptoms such as dizziness and balance deficits (both static and dynamic postural instability) are present in patients with brain injury. These aspects can cause functions limitation and psychological distress, negatively impacting negatively on subjects' quality of life and social reintegration and are considered unfavourable prognostic factors of the recovery process. The literature supports the use of vestibular rehabilitation techniques in patients with mild and moderate brain injury, however, to date, no studies investigated the effect of vestibular rehabilitation in sTBI patients. The main aim of this randomized controlled trail is to verify the effect of a personalized vestibular training on balance and gait disorders in sTBI patients.

Condition or Disease Intervention/Treatment Phase
  • Other: Vestibular Rehabilitation (VR)
  • Other: Conventional Neurorehabilitation
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
30 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Effects of Vestibular Rehabilitation in Patients With Severe Traumatic Brain Injury: a Randomized Controlled Trial
Actual Study Start Date :
Jun 1, 2020
Actual Primary Completion Date :
Feb 26, 2021
Actual Study Completion Date :
Jun 21, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Vestibular Rehabilitation Group

Other: Vestibular Rehabilitation (VR)
VR consisted of two types of exercises, i.e., those for gaze stability and those for postural stability Gaze stability exercises The patients will perform the exercises while holding their gaze on a firm target (VORx1) during active horizontal and vertical head movements (one minute for each axis). Postural stability exercises March in Place Each patient will ask to get on a foam cushion of 10 cm in height and then will blindfold. Treadmill Training As preparation for training, all subjects underwent a 1-minute walk on treadmill with open eyes using preferred walking speed. Immediately after preparation, patients will blindfold and will ask to walk on treadmill without support of hands for 4 minutes. When patients made the mistake of changing direction, the physiotherapist help them to keep the right position using verbal cues (e.g., you are turning left or right).

Active Comparator: Conventional rehabilitation Group

Other: Conventional Neurorehabilitation
muscles stretching, active and assisted limbs mobilization, four limbs coordination exercises, balance training on instable platform and gait training

Outcome Measures

Primary Outcome Measures

  1. Dynamic Gait Index Scoring Form (DGI) [Baseline to 8 weeks after the end training]

    Change of Dynamic Gait Index Scoring Form (DGI) from baseline at 4 weeks of training, at 4 weeks after the end of the training and after 8 weeks after the end of the training. DGI values ranging from 0 to 24, where 0 means the worse outcome and 24 the best one.

Secondary Outcome Measures

  1. Berg Balance Scale (BBS) [Baseline to 8 weeks after the end training]

    Change of Berg Balance Scale (BBS) from baseline at 4 weeks of training, at 4 weeks after the end of the training and after 8 weeks after the end of the training. BBS values ranging from 0 to 56, where 0 means the worse outcome and 56 the best one

  2. Community Balance & Mobility Scale (CB&M) [Baseline to 8 weeks after the end training]

    Change of Community Balance and Mobility Scale (CB&M) from baseline at 4 weeks of training, at 4 weeks after the end of the training and after 8 weeks after the end of the training. CB&M values ranging from 0 to 96, where 0 means the worse outcome and 96 the best one.

  3. Activities-specific Balance Confidence scale (ABC) [Baseline to 8 weeks after the end training]

    Change of Activities-specific Balance Confidence scale (ABC) from baseline at 4 weeks of training, at 4 weeks after the end of the training and after 8 weeks after the end of the training. ABC values ranging from 0% to 100%, where 0% means the worse outcome and 100% the best one.

  4. Community Integration Questionnaire (CIQ) [Baseline to 8 weeks after the end training]

    Change of Community Integration Questionnaire (CIQ) from baseline at 4 weeks of training, at 4 weeks after the end of the training and after 8 weeks after the end of the training. CIQ values ranging from 0 to 29, where 0means the worse outcome and 29 the best one.

  5. Dizziness Handicap Inventory (DHI) [Baseline to 8 weeks after the end training]

    Dizziness Handicap Inventory (DHI) from baseline at 4 weeks of training, at 4 weeks after the end of the training and after 8 weeks after the end of the training. DHI values ranging from 0 to 100, where 100 means the worse outcome and 0 the best one.

  6. Instrumental Assessment [Baseline to 8 weeks after the end training]

    Postural and gait functional assessment performed using inertial motion capture systems (Opal, APDM Inc., Portland, Oregon, USA, portable devices controlling 6 inertial/magnetic measurement units providing 3D orientation and kinematic). The assessments were performed at the baseline, 4 weeks of training, at 4 weeks after the end of the training and after 8 weeks after the end of the training

Eligibility Criteria

Criteria

Ages Eligible for Study:
15 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age between 15 and 65 years;

  • Glasgow coma scale (GCS) score ≤ 8 (used to objectively describe the severity of impaired consciousness at the time of injury)

  • Level of cognitive functioning (LCF) ≥7;

  • Ability to understand verbal commands and the informed consent.

  • Presence of static and dynamic balance impairments.

  • Functional Ambulation Classification (FAC) ≥ 3

Exclusion Criteria:
  • Glasgow coma scale (GCS) score >8

  • Level of cognitive functioning (LCF) <7

  • Inability to understand verbal commands

  • Absence of static and dynamic balance impairments.

  • Functional Ambulation Classification (FAC) < 3

Contacts and Locations

Locations

Site City State Country Postal Code
1 Marco Tramontano Roma Rm Italy 00179
2 Santa Lucia Foundation I.R.C.C.S. Roma Rm Italy 00179

Sponsors and Collaborators

  • I.R.C.C.S. Fondazione Santa Lucia

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Marco Tramontano, head of rehabilitation Services, I.R.C.C.S. Fondazione Santa Lucia
ClinicalTrials.gov Identifier:
NCT04415580
Other Study ID Numbers:
  • FSLCE/PROG.700
First Posted:
Jun 4, 2020
Last Update Posted:
Jun 22, 2021
Last Verified:
Jun 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 22, 2021