Skip to main content
Clinical Trials/NCT06589362
NCT06589362
Recruiting
Not Applicable

Enhancing Cognitive Rehabilitation After TBI Using Noninvasive Vagal Nerve Stimulation

Shirley Ryan AbilityLab1 site in 1 country60 target enrollmentSeptember 7, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Traumatic Brain Injury
Sponsor
Shirley Ryan AbilityLab
Enrollment
60
Locations
1
Primary Endpoint
N-Back Computerized Task
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

The purpose of this study is to examine the feasibility and preliminary efficacy of using transcutaneous auricular vagus nerve stimulation (tVNS) to enhance cognitive recovery in patients with mild-moderate traumatic brain injury (TBI).

Detailed Description

Eligible participants will be invited to two sessions, 2-7 days apart. In each session, either active tVNS or sham stimulation will be administered while the participants are performing tasks of executive functions. The order of the sessions (tVNS vs Sham) will be counterbalanced across participants.

Registry
clinicaltrials.gov
Start Date
September 7, 2024
End Date
August 2026
Last Updated
last year
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Shira Cohen-Zimerman

Research Scientist, PhD

Shirley Ryan AbilityLab

Eligibility Criteria

Inclusion Criteria

  • In inpatient rehabilitation due to recent Traumatic Brain Injury, ages 18-65 years.
  • Ability to independently use a keyboard. Able to understand and communicate in English (according to clinical judgment). Able to independently provide consent to participate. Orientation to place, time, and situation (two consecutive scores of 25 or more on the Orientation Log(O-Log)
  • This scale is routinely administered during acute rehabilitation stay.
  • Exclusion criteria:
  • Acute medical issues requiring close physician or nursing monitoring. Bioelectrical implants, including pacemakers. Pregnancy or persons who are lactating. Significant gross or fine motor weakness. Significant, ongoing communication or comprehension impairments (such as aphasia) that would affect an individual's ability to complete the required assessments.
  • Acute agitation or behavioral issues, as defined by a last Agitated Behavior Scale Score greater than 21 (routinely administered during acute rehabilitation stay, that would affect an individual's ability to participate in the required assessments.
  • Severely impaired memory retention (Score lower than 3 in the 3 Word Delayed Recall test, routinely administered during acute rehabilitation stay.
  • Diagnosis of depression. Active substance abuse.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

N-Back Computerized Task

Time Frame: 15 minutes

In the n-back task, participants are presented a series of visual stimuli. They are asked for each stimulus whether it matches a stimulus n trials before. For example, in a 2-back task, in which the trials consist of letters, participants have to decide whether the current letter is the same as the letter in trial n - 2. We will use a computerized version of this task.

Trail Making Test - Parts A & B

Time Frame: 5 minutes

Trail Making Part A requires participants to draw a line between circles containing numbers in ascending order (e.g., 1-2- 3...etc.). Part B requires participants to alternate drawing a line between ascending letters and numbers (e.g., 1-A-2-B...etc.). The key measures are the time required to complete and the number of errors made in Part A and Part B. This test measures various aspects of cognition including attention, visual search, motor coordination, reasoning, and task-switching.

Study Sites (1)

Loading locations...

Similar Trials