The Utility of Concurrent TBS/fNIRS for Antidepressant Treatment Optimization

Major Depressive Disorder Clinical Trial

Official title:

The Utility of Concurrent TBS/fNIRS for Antidepressant Treatment Optimization

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04526002
• Other study ID #: 15100120
• Status: Recruiting
• Phase: N/A
• Start date: March 1, 2023
• Est. completion date: June 2024

Study information

• Verified date: March 2024
• Source: The Hong Kong Polytechnic University
• Contact: Georg S Kranz, PhD
• Phone: 2766
• Email: georg.kranz[@]polyu.edu.hk
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Repetitive transcranial magnetic stimulation (rTMS) with theta bursts (i.e. TBS) of the dorsolateral prefrontal cortex (DLPFC) is an innovative treatment for major depressive disorder (MDD). Indeed, the U. S. Food and Drug Administration (FDA) has only recently approved TBS (in August 2018). However, fewer than 50% of patients show sufficient response to this treatment; markers for response prediction are urgently needed. Moreover, there is a lack of knowledge of the mechanism of action of TBS of the DLPFC. This is due to difficulties of directly measuring prefrontal stimulation effects, as compared to the stimulation of motor cortex and utilizing motor evoked potentials as direct readout. However, knowledge of immediate DLPFC modulation by TBS is necessary to extrapolate downstream effects on the neural and symptoms level. Thus, there is a need for research that aims to quantify the direct and immediate after-effects of TBS on DLPFC function. Most importantly, with regard to precision medicine, there is a need for research that explores the utility of immediate DLPFC reactivity to TBS for the prediction of antidepressant treatment response. There is common agreement that certain forms of rTMS inhibit or excite brain activity, respectively. However, evidence indicates that there is considerable individual variability in the brain responses to rTMS. Whether differences in individual DLPFC modulation by rTMS can be utilized as a predictive marker for treatment response remains to be investigated. This research program will exploit the combination of functional near-infrared spectroscopy (fNIRS) with brain stimulation. Concurrent TBS/fNIRS measurements will allow us to systematically investigate TBS-induced modulation of blood oxygenation as a proxy for induced brain activity changes. The findings from this study will (1) elucidate the immediate effects of excitatory and inhibitory TBS on prefrontal activity in TBS treatment-naïve patients with MDD and (2) validate the potential utility of TBS-induced brain modulation at baseline for the prediction of antidepressant response to four weeks of daily TBS treatment. Major depression is a severe mental disorder and is associated with considerable economic costs but adequate treatments are poorly explored. This research program will pave the way towards an affordable and easy-to-implement method for response prediction before treatment commencement. Thus, our research proposal has high potential to inform tailored treatment strategies, as envisaged in precision medicine.

Description:

Please refer to the full proposal

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 90
• Est. completion date: June 2024
• Est. primary completion date: June 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 60 Years

Eligibility

MDD group:

Inclusion Criteria:

• MDD (DSM-5), HAMD17 =18, approval for TBS treatment by the physician in charge, stable antidepressive medication 4 weeks before treatment (the sample will include at least 20 drug-naïve patients in order to avoid confounding effects of medication for testing hypothesis 4).

Exclusion Criteria:

• a history of brain surgery, head injury, stroke or neurodegenerative disorder, diagnosis of personality disorder, psychotic features, active suicidal intent, severe somatic comorbidities, cardiac pacemakers, deep brain stimulation, intracranial metallic particles, history of seizures, antiepileptics and benzodiazepines corresponding to a dose of >1 mg lorazepam/d, substance dependence or abuse, if it is the primary clinical problem. HC group:

Inclusion Criteria:

• age between 18 and 60, right-handedness.

Exclusion Criteria:

• a current or previous diagnosis of a psychiatric, neurological disorder or severe internal illness, common contraindications to rTMS,26 and a psychiatric disorder in their first-degree relatives.

Related Conditions & MeSH terms

• Depressive Disorder
• Depressive Disorder, Major
• Major Depressive Disorder

Intervention

Device:
• Theta-burst stimulation (TBS)
TBS comprises 3-pulse 50-Hz bursts, applied every 200 ms (at 5 Hz) as described previously (Huang, Edwards et al. 2005). iTBS consists of 2-second trains with an inter-train-interval of 8 seconds. We will repeat trains (30 pulses; 10 bursts) for 20 times to reach a total number of 600 pulses (3x10x20). cTBS will comprise uninterrupted bursts to reach a total number of 600 pulses, as done routinely by others. Concurrent TBS/fNIRS stimulation will be applied over the left (iTBS) and right (cTBS) DLPFC at an intensity of 70-120%* resting motor threshold (RMT) (The ideal %RMT will be determined first in a pilot study). In part two, stimulation intensity for patients will be 120% RMT (titration to full therapeutic dose over the first three days), as approved by the FDA in the U.S. (Blumbeger et al. 2018). The stimulation site will be the same as in the concurrent TBS/fNIRS stimulation (see above).

Locations

Country	Name	City	State
Hong Kong	The Hong Kong Polytechnic University	Hong Kong

Sponsors (4)

Lead Sponsor	Collaborator
Dr Georg Kranz	Chinese University of Hong Kong, Kowloon Hospital, Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong

Country where clinical trial is conducted

Hong Kong, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Change of Patient Health Questionnaire (PHQ-9, Chinese version) at each treatment day	The score of PHQ-9 ranges from 0 to 27, on which increasing scores represent increasing severity of symptoms	till to end of treatment, up to 18 months
Primary	Response rate after treatment (Montgomery-Asberg depression rating scale, MADRS reduction =50% of baseline)	We will use the MADRS as the primary outcome measure because this symptom rating scale is more sensitive to changes over time. The score of MADRS is ranging from 0 to 60, with higher scores indicative of greater depressive symptomology.	post treatment, up to 22 months
Primary	Oxygenated hemoglobin (HbO) change compared to baseline	TBS-induced HbO change in the DLPFC during and after stimulation	during and post TBS-fNIRS measurement, an average of 2 months. As well as at follow-up, up to 30 months
Secondary	Remission rate after treatment (MADRS=10)	See above	post treatment, up to 22 months
Secondary	Absolute change of mean Hamilton depression rating scale (HAMD17) after 2 and 4 weeks of treatment, as well as at 1 month follow-up	The score of HAMD is ranging from 0 to 53, on which increasing scores represent increasing severity of symptoms	at follow-up, up to 30 months
Secondary	Absolute change of mean Inventory of depression symptomatology-clinician (IDS-C30) after 2 and 4 weeks of treatment, as well as at 1 month follow-up	The score of IDS-C30 ranges from 0 to 84, on which increasing scores represent increasing severity of symptoms	at follow-up, up to 30 months
Secondary	Hb change compared to baseline	TBS-induced Hb change in the DLPFC during and after stimulation	during and post TBS-fNIRS measurement, an average of 2 months. As well as at follow-up, up to 30 months
Secondary	the area under curve of HbO and Hb value during stimulation	TBS-induced HbO and Hb change in the DLPFC during stimulation	during TBS-fNIRS measurement, an average of 2 months. As well as at follow-up, up to 30 months
Secondary	the steepness of the Hb and HbO values change	TBS-induced HbO and Hb change in the DLPFC during stimulation	during TBS-fNIRS measurement, an average of 2 months. As well as at follow-up, up to 30 months