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Clinical Trial of The Boosting Effect of Transcranial Random Noise Stimulation (tRNS) in Cognitive Rehabilitation of Patients With Traumatic Brain Injury

Clinical Trial of The Boosting Effect of Transcranial Random Noise Stimulation (tRNS) in Cognitive Rehabilitation of Patients With Traumatic Brain Injury

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03696381
Acronym
TRUST
Enrollment
30
Registered
2018-10-04
Start date
2019-02-25
Completion date
2020-12-31
Last updated
2019-02-26

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

Conditions

Traumatic Brain Injury, Cognitive Impairment

Keywords

computerized cognitive rehabilitation, trns, traumatic brain injury, tbi, cognitive impairment

Brief summary

The main objective of this study is to evaluate the effects of tRNS while undergoing computerized cognitive rehabilitation therapy to conclude if this combination of therapies would be effective for the cognitive rehabilitation of patients with acquired brain damage, such as traumatic brain injury. We want to study the therapeutic potential of tRNS to enhance the therapeutic outcome of cognitive training, studying its global effect over the rehabilitation of attention, memory and executive functions, compared to sham tRNS.

Interventions

OTHERReal tRNS

The treatment consists of a set of 1-h sessions, three sessions per week for 8 weeks. A series of cognitive exercises of attention, memory, and executive functions will be conducted in each session. During the first 20 minutes of each cognitive training session, patients will receive bi-frontal and bi-parietal tRNS. It has a start and end ramp of two seconds in each case to avoid the slight unpleasant sensation that occurs in the first moments of the introduction of direct current DC.

The treatment consists of a set of 1-h sessions, three sessions per week for 8 weeks. A series of cognitive exercises of attention, memory, and executive functions will be conducted in each session. We will apply a sham tRNS for the first 20 minutes of each cognitive training session. The subjects will receive sham tRNS and will perform the same type of cognitive training as the rest of patients and will receive the same type of adverse reaction questionnaire. Subjects receiving simulated stimulation will receive the same type of ramps at the beginning and end of the session to ensure triple-blind maintenance .

Sponsors

Institut Guttmann
Lead SponsorOTHER

Study design

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

Eligibility

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

Inclusion criteria

* age over 18 years old * documented history of severe or moderate TBI (severe TBI: Glasgow Coma Scale 3-8; moderate TBI: Glasgow Coma Scale 9-13) * out of post-traumatic amnesia * less than 6 months after TBI * cognitive impairment objectified by neuropsychological exploration.

Exclusion criteria

* impairment of language, affecting the production and/or comprehension of speech and the ability to read and/or write * severe alteration of the visual field or visual perception problems that limits the use of technological devices * sever motor impairment of both upper extremities that prevent the use of technological devices * previous or current history of psychiatric, neurological or systemic alterations that affect the central nervous system * history of substance abuse * dermatological diseases in the skull * presence of metal implants or holes in the skull * epilepsy.

Design outcomes

Primary

MeasureTime frameDescription
Spanish phonemic fluency test (PMR)1 dayTo improve performance in phonemic fluency after receiving experimental intervention.
Digit Span Forward from the Wechsler Adult Intelligence Scale1 dayTo improve performance in span of immediate verbal recall after receiving experimental intervention.
Digit Span Backward from the Wechsler Adult Intelligence Scale1 dayTo improve performance in working memory after receiving experimental intervention.
Rey Auditory Verbal Learning Test1 dayTo improve performance in short-term, long-term and recognition.
Letters and Numbers from the Wechsler Adult Intelligence Scale1 dayTo improve performance in working memory after receiving experimental intervention.
Conners Continuous Performance Test (CPT-II)1 dayTo improve performance in sustained attention after receiving experimental intervention.

Secondary

MeasureTime frameDescription
Trail Making Test B (TMT-B)1 dayTo improve performance in task-switching
Wisconsin Card Sorting Test (WCST)1 dayTo improve performance in set-shifting
Stroop Color and Word test (Stroop Test)1 dayTo improve performance in inhibitory control
Trail Making Test A (TMT-A)1 dayTo improve performance in visual attention

Countries

Spain

Contacts

Primary ContactAdria Garcia Rosas
adriagarcia@guttmann.com934977700

Outcome results

None listed

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