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Behavioral Intervention

Brain Training for Spinal Cord Injury (SCI-IQ Trial)

N/A

Recruiting

Led By Erica Weber, PhD

Research Sponsored by Kessler Foundation

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

18-65 years old

Be older than 18 years old

Must not have

No significantly impairing visual disturbance

Timeline

Screening 3 weeks

Treatment Varies

Follow Up baseline to immediate post-treatment (week 13) and long-term follow-up (week 25)

Summary

"This trial aims to see if a brain training program can help people with recent spinal cord injuries improve how quickly they process information."

Who is the study for?

This trial is for individuals who have recently suffered a traumatic spinal cord injury and are experiencing cognitive impairments, specifically with processing speed. The detailed inclusion and exclusion criteria are not provided.

What is being tested?

The study is testing the effectiveness of game-like computerized activities designed to improve information processing speed in those with acute spinal cord injuries.

What are the potential side effects?

Since this trial involves cognitive training programs, traditional physical side effects may not apply. However, participants might experience fatigue or frustration during the activities.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Select...

I am between 18 and 65 years old.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:

Select...

I do not have major problems with my vision.

Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ baseline to immediate post-treatment (week 13) and long-term follow-up (week 25)

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~baseline to immediate post-treatment (week 13) and long-term follow-up (week 25)

This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline to immediate post-treatment (week 13) and long-term follow-up (week 25) for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.

Primary study objectives

Letter and Pattern Comparison (LPC)

Symbol Digit Modalities Test (SDMT)

Useful Field of View (UFOV)

Secondary study objectives

Spinal Cord Injury Quality of Life scales (SCI-QOL)

Trial Design

2Treatment groups

Experimental Treatment

Placebo Group

Group I: ExperimentalExperimental Treatment1 Intervention

pre-specified computer tasks using an Internet-based cognitive training portal, to be completed 3x per week for 60 minutes each session for 12 weeks total

Group II: Placebo ControlPlacebo Group1 Intervention

pre-specified computer tasks using an Internet-based cognitive training portal, to be completed 3x per week for 60 minutes each session for 12 weeks total

0 / 2Eligibility criteria met