Image

Robot-assisted Training After Traumatic Brain Injury and Disorders of Consciousness

Recruiting
18 years of age
Both
Phase N/A

Overview

The goal of this randomised cross-over feasibility trial is to investigate two intensive robot-assisted training therapies in the early rehabilitation phase after traumatic brain injury and disorders of consciousness. The main questions it aims to answer are:

  • Is the protocol feasible concerning inclusion in the study?
  • Is the protocol feasible concerning protocol completion? Participants will randomly be assigned to either five days of robot-assisted gait training (GAIT), two days of pause, then five days of robot-assisted step training (STEP) or vice versa.

The investigators will explore and compare safety events, physiological measures and physical activity levels, behavioural measures, and functional disability outcomes. Further, the investigators report intervention and technical parameters in detail.

Description

This is a randomised cross-over feasibility trial, carried out according to the Helsinki Declaration and approved by the scientific ethics committee of the Capital Region, Denmark. Participants are temporarily unable to consent why this obtained from the next of kin.

Participants start the intervention when 10 minutes of standing in a tilt-table does not cause orthostatic hypotension. Participants then recieve five days of intervention, two days pause and then cross over to the other intervention.

Groups
  1. GAIT --> STEP
  2. STEP --> GAIT

Eligibility

INCLUSION CRITERIA

  • Admitted for rehabilitation at the Department of Brain and Spinal Cord Injury, Division of Brain Injury, Bodil Eskesen Centre, Rigshospitalet
  • Patients 18 years or older
  • In the unresponsive wakefulness or minimally conscious state after a moderate to severe Traumatic brain injury (ICD 10, DS06)
  • Obtained consent from nearest relative and study guardian.

EXCLUSION CRITERIA

  • Weight > 135 kg (maximum weight for the Erigo® tilt table)
  • Height > 200 cm (maximum height for the Lokomat®)
  • In the confusional state or emerged to full consciousness
  • If weight bearing is restricted due to, e.g., fractures of the spine, pelvis, or lower limbs.
  • Known osteoporosis of a severity where use of robotic orthoses, according to a physician, is considered a contraindication
  • If lower limb joints are fixated to a degree that cannot be compensated in the orthoses
  • No valid consent from the nearest relative or study guardian

Study details

Traumatic Brain Injury, Disorders of Consciousness

NCT06343415

Christina Kruuse

14 May 2024

Rewrite in simple language using AI

Step 1 Get in touch with the nearest study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar

Primary Contact

site

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.