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The Development of a Virtual Reality Program to Improve Attention in Individuals With TBI

The Development of a Virtual Reality Program to Improve Attention in Individuals With TBI

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03605017
Enrollment
32
Registered
2018-07-30
Start date
2014-03-26
Completion date
2022-03-26
Last updated
2021-10-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

TBI (Traumatic Brain Injury)

Keywords

cognitive rehabilitation, attention, executive function

Brief summary

The purpose of this research is to investigate the effectiveness of a technique designed to improve divided attention and set-shifting impairments in persons with a traumatic brain injury (TBI). The study is designed to evaluate how well this technique can help people with TBI increase their attention and ability to function better in everyday life.

Detailed description

A pilot study will be conducted to evaluate the effectiveness of a technique designed to improve higher level attention (switching between tasks and multi-tasking) for persons with a traumatic brain injury. 32 individuals with TBI will be recruited. Baseline assessment includes neuropsychological evaluation using traditional measures as well as a completion of a number of questionnaires designed to measure everyday attention and everyday functioning. Participants are random assigned to either the experimental or control groups. Experimental and control treatments include two 60 minute sessions, twice per week, for 5 weeks. Follow-up assessment includes a neuropsychological evaluation using traditional measures as well as a completion of a number of questionnaires designed to measure everyday attention and everyday functioning. Protocol efficacy will be determined by improvements between baseline and follow-up on several objective and functional measures of divided attention and set-shifting.

Interventions

BEHAVIORALVirtual Reality Executive Function Training (VREFT)

Sponsors

National Institute on Disability, Independent Living, and Rehabilitation Research
CollaboratorFED
Kessler Foundation
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* between the ages of 18-65 * diagnosis of TBI * can read and speak English fluently

Exclusion criteria

* prior stroke or neurological disease other than TBI * unstable or uncontrolled seizures * currently taking benzodiazepines

Design outcomes

Primary

MeasureTime frameDescription
Total divided attention post-treatment (covarying for baseline performance)7 weeks (between pre- and post-testing)Comparison between treatment and control groups on post-treatment Auditory Consonant Trigrams
Total set-shifting post-treatment (covarying for baseline performance)7 weeks (between pre- and post-testing)Comparison between treatment and control groups on post-treatment Stroop interference

Countries

United States

Contacts

Primary ContactDenise Krch, PhD
dkrch@kesslerfoundation.org973-324-8392
Backup ContactAngela Smith, BA
asmith@kesslerfoundation.org9733248448

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026