Aquatic Sequential Preparatory Approach and Severe Traumatic Brain Injury

Sponsor
I.R.C.C.S. Fondazione Santa Lucia (Other)
Overall Status
Completed
CT.gov ID
NCT04383405
Collaborator
(none)
20
1
2
8
2.5

Study Details

Study Description

Brief Summary

Traumatic brain injury (TBI) is an acquired insult to the brain from an external mechanical force. It is considered a major cause of mortality and of long-term disabilities in young adults, especially considering high-income countries.

The TBI can cause a wide range of temporary and/or permanent brain's dysfunctions that can involve physical, cognitive, behavioural and emotional functioning limiting everyday life and social activities and leading to a lowers quality of life.

a sequential preparatory approach (SPA), performed in aquatic environment, based on increasing difficulty and following a specific sequence of preparatory exercises (from the simplest to the most complex) could be an effective complementary training during post-acute intensive rehabilitation in patients with severe traumatic brain injury (sTBI).

Condition or Disease Intervention/Treatment Phase
  • Other: Aquatic Training
  • Other: Conventional Training
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
20 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Aquatic Therapy During Post-acute Intensive Neurorehabilitation in Patients With Severe Traumatic Brain Injury: a Preliminary Randomized Controlled Trial
Actual Study Start Date :
Sep 1, 2019
Actual Primary Completion Date :
Apr 19, 2020
Actual Study Completion Date :
May 2, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Sequential Preparotory Approach

Other: Aquatic Training
Aquatic Training training consists of a sequential and a preparatory approach aimed at enhancing dynamic postural stability. The exercises follow a specific sequence starting from a kneeling position, proceeding to a sitting position and ending with a supine position. Step exercises preparatory for gait were performed using a step and two floating aids. Gait exercises were performed first with the upper limbs placed on two floating aids and then during a dual motor task (i.e. catching a ball thrown by the therapist). Subjects performed three sessions a week for four weeks and each session lasting 45 minutes. The training was carried out by a physiotherapist who had at least 5 years of experience in aquatic neurorehabilitation.

Active Comparator: Conventional

Other: Conventional Training
Conventional land-based therapy consists of customized exercises focused on static and dynamic postural stability improvement. The exercises included the active-assisted mobilization, the muscle stretching the postural transition, the balance and the gait training. The control approach was carried out three times a week for four weeks and each session lasted 45 minutes.

Outcome Measures

Primary Outcome Measures

  1. Change in Berg Balance Scale (BBS) at 1month [1 month]

    Change of Berg Balance Scale (BBS) from baseline at 1 month. BBS values ranging from 0 to 56, where 0 means the lowest level of function and 56 the highest

Secondary Outcome Measures

  1. Tinetti Balance and Gait Scale (TBG) [baseline and after 4 weeks of training]

    Change of Tinetti Balance and Gait Scale (TBG) from baseline at 4 weeks of training and at 4 weeks after the end of the training. TBG values ranging from 0 to 28, where 0 means the worse outcome and 28 the best one.

  2. Modified Barthel Index (MBI) [baseline and after 4 weeks of training]

    Change of Modified Barthel Index (MBI) from baseline at 4 weeks of training and at 4 weeks after the end of the training. MBI values ranging from 0 to 105, where 0 means the worse outcome and 105 the best one.

  3. Modified Ashworth Scale (MAS) [baseline and after 4 weeks of training]

    Change of Modified Ashworth Scale (MAS) from baseline at 4 weeks of the training and at 4 weeks after the end of the training. MAS values ranging from 0 to 5, where 0 means the best outcome and 5 the worse one.

  4. Change in quality of life assessed by the proxy version of the Quality of Life after Brain Injury (Proxy-QOLIBRI) [baseline and after 4 weeks of training]

    Change of proxy version of the Quality of Life after Brain Injury (Proxy-QOLIBRI) from baseline at 4 weeks of training and at 4 weeks after the end of the training. (Proxy-QOLIBRI) values ranging from 0 to 100, where 0 means the worse outcome and 100 the best one.

  5. Disability Rating Scale (DRS) [baseline and after 4 weeks of training]

    Measure of function after TBI intended to measure function from "coma to community." Minimum score= 0; Maximum score= 29 (High scores are indicative of greater degree of disability).

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.

  • acclimatization to water.

Exclusion Criteria:
  • Cognitive deficits affecting the ability to understand task instructions (Mini-Mental State Examination > 24);

  • Severe unilateral spatial neglect (diagnosed with a test battery that included the Letter Cancellation test, Barrage test, Sentence Reading test and the Wundt-Jastrow Area Illusion Test);

  • Severe aphasia (diagnosed by means of neuropsychological assessment);

  • Presence of other neurological diseases;

  • Presence of cutaneous and mycosis infections;

  • Presence of open wounds, eczema, skin ulcers, decubitus lesions, severe burns;

  • Presence of PEG (Percutaneous endoscopic gastrostomy);

  • Presence of tracheostomy;

  • Urinary incontinence;

  • Presence of otitis

  • Presence of orthopedic or cardiac comorbidities that would limit participation in the experimental and conventional training (all of which were clinically evaluated).

Contacts and Locations

Locations

Site City State Country Postal Code
1 Marco Tramontano Rome 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:
NCT04383405
Other Study ID Numbers:
  • CE/PROG775/2019SPA
First Posted:
May 12, 2020
Last Update Posted:
May 12, 2020
Last Verified:
May 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
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 May 12, 2020