Feasibility of a Motor-cognitive Training Program in Patients With Traumatic Brain Injury

Sponsor
Swiss Federal Institute of Technology (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06149975
Collaborator
Cantonal Hospital St. Gallen (Other)
30
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1
7.3
4.1

Study Details

Study Description

Brief Summary

The goal of this clinical study is to test feasibility of a motor-cognitive training program in patients after mild to severe traumatic brain injury in an acute hospitalization setting.

The intervention is a step-based dual-task training, i.e. patients are presented with step patterns that they have to memorize and then execute in the tempo given by a metronome.

Researchers will assess the feasibility of the motor-cognitive training regarding acceptance and safety, user evaluation of the training and training performance.

Condition or Disease Intervention/Treatment Phase
  • Other: motor-cognitive training
N/A

Detailed Description

A traumatic brain injury (TBI) refers to a functional disorder of the brain with or without demonstrable injuries to the brain as a result of external force to the skull and/or brain. The most common causes are traffic accidents and falls. After TBI, impairments may occur in motor skills such as gait stability, static and dynamic balance and motor coordination as well as cognitive skills such as memory, dual- and multi-tasking (DT/MT), and psychomotor speed. Therefore, rapid improvement of motor and cognitive functioning and falls prevention are essential.

Dual-task training have been shown to improve gait performance and to reduce the risk of falling in some neurological disorders, such as Parkinson's disease and stroke. Although there are differences in the underlying pathophysiology between these neurological conditions and TBI, research has identified many common fall-risk factors and thus it can be expected that TBI patients would also profit from cognitive-motor dual-task training. However, research on the effects of such training in TBI patients in scarce. To our knowledge, there is only one study that has looked into the effects of dual-task motor-cognitive training in people with neurological conditions, including (but not specifically for) persons with TBI. For this reason, this study aims to assess the feasibility of a concept for stepping training (StepIt) that addresses motor as well as cognitive falls-related aspects in patients with TBI.

This study will be conducted as one-arm, monocentric intervention trial. After admission to the normal ward, patients potentially fulfilling the eligibility criteria will be informed orally and in writing about the study and asked if they wish to participate. All interested participants will then be screened for final inclusion. Baseline data collection will occur prior to the first training session and training evaluation will be conducted after 3 to max. 10 trainings (depending on the length of their hospital stay). During each training session individual training parameters will be documented. In addition to the usual care, the study participants receive the motor-cognitive training "StepIt". The "StepIt" will be conducted as an approximately 15-minute one on one training for at least 3 to max. 10 sessions during the stay at the hospital.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Feasibility of a Motor-cognitive Training Program in Patients With Traumatic Brain Injury During Acute Hospitalization
Anticipated Study Start Date :
Nov 20, 2023
Anticipated Primary Completion Date :
Jun 30, 2024
Anticipated Study Completion Date :
Jun 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

In addition to the usual care, the study participants receive the motor-cognitive training "StepIt". The "StepIt" will be conducted as an approximately 15-minute one on one training for at least 3 to max. 10 sessions during the stay at the hospital.

Other: motor-cognitive training
The motor-cognitive training in this study will be conducted in form of a step-based dual-task training. A mat (approximately 90 x 90 cm) made from extra non-slip yoga mats is required. The mat is divided into 9 equal squares with a 3 x 3 pattern. Participants will be presented with stepping patterns which they must memorize and then execute on the mat in the pace given by a metronome. All participants will start at the same level. The progression will be adjusted individually according to the fixed criteria of the "StepIt" concept within the sessions. All sessions will be supervised by at least one physical therapist.

Outcome Measures

Primary Outcome Measures

  1. Recruitment rate [through study completion, an average of 9 months]

    Number of patients fitting to the inclusion exclusion (resp. exclusion) criteria as percentages of persons with TBI admitted in the hospital during the study period

  2. Inclusion rate [through study completion, an average of 9 months]

    Number of patients included in the study as percentages of patients fitting to the inclusion (resp. exclusion) criteria

  3. Attrition rate [through study completion, an average of 9 months]

    Number of Drop-outs as percentages of patients included in the study

  4. Adherence rate [through study completion, an average of 9 months (over all training sessions)]

    Number of attended training sessions as percentages of total possible training sessions

  5. Compliance rate [through study completion, an average of 9 months (over all training sessions)]

    Number of attended training minutes as percentages of the total possible training minutes

  6. Security incidents [through study completion, an average of 9 months (over all training sessions)]

    Total number of (Serious) Adverse Events (SAE/AE)

Secondary Outcome Measures

  1. Physical and cognitive load [through study completion, an average of 9 months (after each training session (min. 3 times max. 10 times))]

    Physical and cognitive load assessed with the National Aeronautics and Space Administration-Task Load Index (NASA-TLX). The NASA-TLX is a self-report, multidimensional assessment tool that rates perceived workload in order to assess a task, a system, or other aspects of performance (in this case the "StepIi" trainings). It contains five subscales: Mental Demand, Physical Demand, Temporal Demand, Performance, Effort and Frustration. Each subscale can be given a score between 0 and 20. A higher score reflects a higher workload.

  2. Patient Satisfaction [through study completion, an average of 9 months (after each training session (min. 3 times max. 10 times))]

    With a tailored (self-made) usability questionnaire the patient satisfaction will be assessed. The questionnaire records how the participants felt about the training, how satisfied they were with the training and whether they would recommend the training to others. The questionnaire contains 13 questions (Yes-No questions, Likert-Scale, and open questions). Each item will be evaluated separately.

  3. Improvement [through study completion, an average of 9 months (after each training session (min. 3 times max. 10 times))]

    Comparison of the entry level versus the highest achieved level in percentage (for following training parameters: i. length of stepping sequence, ii.beats/minute, iii. Stepping sequence complexity)

  4. Training capacity [through study completion, an average of 9 months (after each training session (min. 3 times max. 10 times))]

    Number of taught patterns per training session

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • People diagnosed with mild (Glasgow Coma Scale 14-15), moderate (Glasgow Coma Scale 9-13) or severe (Glasgow Coma Scale 3-8) TBI

  • Age ≥ 18 years

  • Planned hospital treatment >24h on regular ward (non-ICU)

  • Physically able to stand (using cane if needed)

  • Able to give informed consent

Exclusion Criteria:
  • Limited vision and hearing ability (except facial injuries with monocular swelling)

  • Inability or contraindications to undergo the investigated intervention.

  • ICU stay only

  • Montreal Cognitive Assessment (MoCa) score < 16

Contacts and Locations

Locations

Site City State Country Postal Code
1 Cantonal Hospital of St. Gallen Saint Gallen Switzerland 9000

Sponsors and Collaborators

  • Swiss Federal Institute of Technology
  • Cantonal Hospital St. Gallen

Investigators

  • Study Director: Anne-Katrin Hickmann, PD Dr., Cantonal Hospital St. Gallen

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Eleftheria Giannouli, Principal Investigator, Swiss Federal Institute of Technology
ClinicalTrials.gov Identifier:
NCT06149975
Other Study ID Numbers:
  • StepIt TBI
First Posted:
Nov 29, 2023
Last Update Posted:
Nov 29, 2023
Last Verified:
Nov 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Eleftheria Giannouli, Principal Investigator, Swiss Federal Institute of Technology
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 29, 2023