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TBS,TMS, Suicidal Ideation, Magnetic Resonance Imaging, Dorsolateral Prefrontal Cortex, Ventrolateral Prefrontal Cortex

Theta Burst Stimulation, Transcranial Magnetic Stimulation, Late Life Depression, Suicidal Ideation, Functional Magnetic Resonance Imaging, Dorsolateral Prefrontal Cortex, Ventrolateral Prefrontal Cortex

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05010915
Enrollment
125
Registered
2021-08-18
Start date
2021-11-01
Completion date
2024-09-30
Last updated
2024-08-22

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

Conditions

Late Life Depression

Keywords

TMS, TBS

Brief summary

Transcranial magnetic stimulation (TMS) is a noninvasive brain stimulation technique, its approved therapeutic indication is high-frequency stimulation to the left dorsolateral prefrontal cortex (DLPFC) for treatment resistant.

Detailed description

investigators design a prospective three-year study to exam the effect of TBS on reducing suicidality targeted at left DLPFC vs VLPFC, and guided by task fMRI neuronavigation and sham. Investigators will adopt personalized left DLPFC and VLPFC localization from baseline task fMRI data. Due to the global brain atrophic changes in the older adults, this issue has been even more important. Investigators will enroll 163 late life depression cases, they will be randomly allocated to either DLPFC group (65 cases), or VLPFC group (65 cases) and sham group (33 cases). To sum up, investigators seek to evaluate the impact of an acute course of TBS guided by tsked fMRI neuronavigation on suicidal ideation, and through follow-up for 6 months, investigators expect to examine (1) suicidal ideation, structural and functional brain differences, inflammatory markers pre/post TBS treatment, explore the link between the mechanism underlying of TBS on brain connectivity and therapeutic effects (2) Association of suicide ideation and neurocognitive function, inflammatory factors and brain imaging data. Exploratory analysis will assess suicide ideation as mediator in the association of neurocognitive deficit and functional connectivity or neurocognitive deficit as mediator in the association of suicide ideation and brain imaging data (3) The trajectories of suicidal ideation in late life depression, to analysis whether the association of cognitive dysfunction and suicidal ideation occurs across time and the prediction of neurocognitive function.(4) Explore the association of suicidal ideation the depression severity, to test if suicidal ideation could be an independent treatment target (5) Investigate the plausible predictors of neuropsychological profiles or neuroimaging findings associated to the effect of TBS in reducing suicidal ideation, which could provide a more efficient strategy for suicide prevention in the elder.

Interventions

DEVICETranscranial magnetic stimulation

Transcranial magnetic stimulation

Sponsors

Chang Gung Memorial Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Age \> 50 years. 2. Major depressive disorder (MDD). 3. Right handiness 4. with a score ≥ 12 on the Beck Scale of Suicidal Ideation (BSSI) and a score of at least 3 on Question #3 (Suicide: 3 ideas and gestures of suicide) of the HAMD

Exclusion criteria

1. Inability to provide informed consent. 2. Dementia, as defined by MoCA 23/24. Other major mental or current psychotic symptoms 3. Active current suicidal intent as evidenced or the endorsement of an actual attempt, interrupted attempt, 4. Have known preexisting noise-induced hearing loss, concurrent treatment with ototoxic medications, or with cochlear implants are on medications known to lower seizure threshold. 5. Alcohol or other substances abuse of or dependence on within the past 3 months Organic brain, head trauma, 6. Elevated risk of seizure due to TBI 7. Participation in concurrent clinical trial 8. Non-correctable clinically significant sensory impairment (i.e., cannot hear well enough to cooperate with interview). 9. Unstable medical illness, including delirium, malignancy, uncontrolled diabetes mellitus, hypertension, hyperlipidemia, or cerebrovascular or cardiovascular risk factors that are not under medical management. Unstable cardiac disease or recent (\<3m) myocardial infarction 10. Mental implement in the brain, claustrophobia 11. Ever received ECT, TMS Consent procedures.

Design outcomes

Primary

MeasureTime frameDescription
Beck Scale for Suicide Ideation (BSSI) at baselinebaseline(1 week before treatment)the severity of suicide ideation(the score range from 0-38,the higher score indicates higher severity.
Beck Scale for Suicide Ideation (BSSI)at the 1st monththe 1st month (4 weeks after baseline)the severity of suicide ideation(the score range from 0-38,the higher score indicates higher severity)
Beck Scale for Suicide Ideation (BSSI)at the 3rd monththe 3rd month(12 weeks after baseline)the severity of suicide ideation(the score range from 0-38,the higher score indicates higher severity)
Beck Scale for Suicide Ideation (BSSI)at the 6th monththe 6th month(24 weeks after baseline)the severity of suicide ideation(the score range from 0-38,the higher score indicates higher severity)

Secondary

MeasureTime frameDescription
Diffusion Tensor Imaging (DTI) - FAbaseline(1 week before treatment), the 1st month(4 weeks after baseline)Fractional anisotropy (FA) is a measurement used in DTI, which reflects the movement of water molecules. FA ranges from 0 to 1, the higher FA value may represent more intact axons.reflects the neural activity.
Verbal Learning & Memory:baseline(1 week before treatment), the 1st month(4 weeks after baseline) and the 6th month(24 weeks after baseline)Word list of Wechsler Memory Scale-III Face memory task
Interleukin-1baseline(1 week before treatment), the 1st month(4 weeks after baseline)IL-1
Interleukin-2baseline(1 week before treatment), the 1st month(4 weeks after baseline)IL-2
Interleukin-6baseline(1 week before treatment), the 1st month(4 weeks after baseline)IL-6
Interleukin-10baseline(1 week before treatment), the 1st month(4 weeks after baseline)IL-10
Geriatric Depression Scalebaseline(1 week before treatment), the 1st month(4 weeks after baseline), the 3rd moth(12 weeks after baseline), and the 6th month(24 weeks after baseline)the severity of depression(the score range from 0-15,the higher score means worse outcome)
Interleukin-1βbaseline(1 week before treatment), the 1st month(4 weeks after baseline)IL-1β
C-Reactive proteinbaseline(1 week before treatment), the 1st month(4 weeks after baseline)CRP
cortisolbaseline(1 week before treatment), the 1st month(4 weeks after baseline)cortisol
thyrotropinbaseline(1 week before treatment), the 1st month(4 weeks after baseline)TSH
Brain-derived neurotrophic factorbaseline(1 week before treatment), the 1st month(4 weeks after baseline)BDNF
Tumor necrosis factorbaseline(1 week before treatment), the 1st month(4 weeks after baseline)TNF-α
structural and functional connectivitybaseline(1 week before treatment), the 1st month(4 weeks after baseline)Brain MRI connectivity change
MRI T1baseline(1 week before treatment), the 1st month(4 weeks after baseline)Brain structural volumes (cm)
functional MRI (resting-state/biological motion task) - BOLD signalbaseline(1 week before treatment), the 1st month(4 weeks after baseline)Blood-oxygen-level-dependent (BOLD) signal is a measurement used in fMRI which reflects the neural activity.

Countries

Taiwan

Contacts

Primary ContactShwu-Hua Lee
shlee@cgmh.org.tw03-3281200
Backup Contacthsueh-ching tsai, bachelor
stacy.tsai409@gmail.com03-3281200

Outcome results

None listed

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