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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03453125
Other study ID # R-799-13
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date September 25, 2013
Est. completion date September 30, 2022

Study information

Verified date December 2021
Source Kessler Foundation
Contact Denise Krch, PhD
Phone 973-324-8392
Email dkrch@kesslerfoundation.org
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this study is to establish that a memory retraining protocol, originally developed for English-speakers, and translated into Spanish, is effective.


Description:

A pilot study will be conducted to carry out this validation and resolve any methodological concerns in the translated protocol. 20 Spanish-speaking Hispanics at least one year post-traumatic brain injury (TBI) and 20 Spanish-speaking Hispanics with multiple sclerosis (MS), both with an objective deficit in learning and memory will be recruited. Baseline assessment includes neuropsychological evaluation using traditional measures as well as completion of a number of questionnaires designed to measure everyday memory and everyday functioning. Subjects are randomly assigned to either the experimental or control groups. Experimental and control treatments includes two 45-60 minute sessions, twice per week, for 5 weeks. Follow-up assessment includes a neuropsychological evaluation using traditional measures as well as completion of a number of questionnaires designed to measure everyday memory and everyday functioning. Protocol efficacy will be determined by improvements between baseline and follow-up on an objective measure of learning and memory.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date September 30, 2022
Est. primary completion date September 30, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - between the ages of 18 and 65 - Spanish is my dominant language, and I have had a traumatic brain injury or I have multiple sclerosis. Exclusion Criteria: - Participants with major depressive disorder, schizophrenia, bipolar disorder I or II - MS subjects: Individuals with a history of head injury, stroke, seizures, or any other significant neurological history will not be included in the study. - TBI subjects: Individuals must have sustained a TBI at least one year prior to enrollment in the study protocol. Individuals with a history of significant neurological insult other than TBI (e.g. premorbid epilepsy, multiple sclerosis, Alzheimer's disease) will not be included in the study.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Spanish modified Story Memory Technique (mSMT)


Locations

Country Name City State
Spain Hospital Aita Menni Arrasate-Mondragón
United States Kessler Foundation East Hanover New Jersey

Sponsors (2)

Lead Sponsor Collaborator
Kessler Foundation Instituto Vocacional Enrique Díaz de León A.C., Guadalajara, Mexico

Countries where clinical trial is conducted

United States,  Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Total learning post-treatment (covarying for baseline performance) Comparison between treatment and control groups on post-treatment Hopkins Verbal Learning Test (HVLT) learning score, covarying for baseline HVLT performance. 7 weeks (between pre- and post testing)