Feasibility of a Motor-cognitive Training Program in Patients With Traumatic Brain Injury During Acute Hospitalization
motor-cognitive training
Brain Injuries, Traumatic+5
+ Brain Diseases
+ Brain Injuries
Other Study
Summary
Study start date: November 20, 2023
Actual date on which the first participant was enrolled.This study focuses on testing a new training program called "StepIt" for patients who have suffered a traumatic brain injury (TBI). TBI often results from accidents or falls and can lead to issues with movement, balance, and thinking skills such as memory and multitasking. The goal of this study is to see if a specific type of training that combines movement and cognitive tasks can help improve these abilities in TBI patients, potentially reducing their risk of falls. Given the limited research on such training for TBI patients, this study aims to fill that gap and explore whether this approach is feasible and beneficial. Participants in the study are patients who are hospitalized after a TBI and meet certain eligibility criteria. They will undergo a series of training sessions using the "StepIt" program, which is a short, personalized training lasting about 15 minutes. This training is done alongside the usual care they receive in the hospital. The study will gather initial data before the training starts and evaluate the outcomes after 3 to 10 sessions, depending on how long patients stay in the hospital. Each session's details are recorded to ensure the training is being applied effectively. The focus is on assessing the practicality of the training and its impact on patients' motor and cognitive functions.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.7 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Other Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Cantonal Hospital of St. Gallen
Sankt Gallen, SwitzerlandOpen Cantonal Hospital of St. Gallen in Google Maps