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Modified Story Memory Technique (mSMT) in Persons With TBI

A Randomized Clinical Trial Examining The Efficacy of The Group Administered Modified Story Memory Technique (mSMT) in Persons With TBI

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04056312
Enrollment
45
Registered
2019-08-14
Start date
2016-06-29
Completion date
2022-06-30
Last updated
2026-07-22

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

Conditions

Traumatic Brain Injury

Keywords

memory, learning, cognition, traumatic brain injury, treatment and therapy

Brief summary

The current RCT is designed to: 1. test the efficacy of the group based mSMT in persons with TBI on NPE, the current gold-standard for measuring memory functioning 2. assess the effectiveness of the group mSMT on more global measures of everyday life, including an objective measure shown through our previous work to be sensitive to memory changes following the mSMT, as well as additional questionnaires to be completed by both the participant and a significant other 3. evaluate the changes in brain functioning following treatment with the mSMT via fMRI and 4. evaluate the long-term effects of the treatment protocol. To accomplish these goals investigators will conduct a double-blind, placebo-controlled, RCT, applying the group mSMT to a sample of 60 participants with moderate to severe TBI (30 treatment; 30 control).

Detailed description

Outcome measures will assess objective memory abilities, everyday memory abilities and patterns of cerebral activation during learning. A long-term follow-up assessment will be conducted, designed to measure the impact of the mSMT 3 months following treatment completion. Alternate forms will be utilized wherever available.

Interventions

BEHAVIORALGroup Memory retraining exercises

Experimental group will be receiving memory retraining exercises via lap top twice a week for 5 weeks. Four people in a group.

BEHAVIORALPlacebo controlled group memory exercise training

Placebo group will be receiving memory retraining exercises via lap top twice a week for 5 weeks. Four people in a group.

Sponsors

Kessler Foundation
Lead SponsorOTHER
United States Department of Defense
CollaboratorFED

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

* I am between the ages of 18-65. * I have had a Traumatic Brain Injury at least one year ago. * I can read and speak English fluently. * I have difficulties with learning and memory skills.

Exclusion criteria

* I am currently taking steroids and /or benzodiazepines as determined by study staff review of my medications. * I have had a prior stroke or neurological injury/disease other than a traumatic brain injury. * I have a history of significant psychiatric illness (for example, bipolar disorder or psychosis) or a current diagnosis of Major Depressive Disorder, Schizophrenia, Bipolar Disorder I or II. * I have unstable or uncontrolled seizures. * I have a significant alcohol or drug abuse history.

Design outcomes

Primary

MeasureTime frameDescription
California Verbal Learning TestChange will be assessed. Scales will be administered at 3 time points;pretreatment immediately following 5 months laterChange on scores on memory tests will be assessed using the California Verbal Learning Test
The Traumatic Brain Injury-Quality of Life ScaleChange will be assessed. Scales will be administered at 3 time points;pretreatment immediately following 5 months laterSelf-reports of emotional functioning, memory functioning and quality of life on The Traumatic Brain Injury-Quality of Life Scale, which measures these constructs. DVs will be change on the Depression subscale (range: 0-40; lower score is better) and Cognition scale (range: 0-40; higher score is better).

Countries

United States

Contacts

STUDY_CHAIRRichard Green, PhD

Kessler Foundation

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 23, 2026