Probing Homeostatic Plasticity With Priming Theta-burst Stimulation of the Dorsolateral Prefrontal Cortex
Primary Purpose
Depression Minor
Status
Recruiting
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
Theta-burst stimulation (TBS)
Sponsored by
About this trial
This is an interventional basic science trial for Depression Minor
Eligibility Criteria
Inclusion Criteria:
- age 18-35
- education level of primary six or above
- right-handedness
- normal or corrected-to-normal vision
- being able to understand the verbal instructions
- willingness to sign the informed consent form
Exclusion Criteria:
- a history of seizures
- current or past psychiatric disorders
- current or past severe internal or neurological illness
- ferromagnetic implants <20cm from the head, cardiac pacemaker, deep brain stimulation and other common TMS exclusion criteria
- history of substance dependence or abuse within the last 3 months
- intake of any medication known to affect the excitation threshold (i.e., benzodiazepines, anticonvulsants).
Sites / Locations
- The Hong Kong Polytechnic UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Experimental
Experimental
Experimental
Experimental
Arm Label
Condition 1
Condition 2
Condition 3
Condition 4
Arm Description
Priming sham TBS, followed by iTBS after an inter-stimulation-interval (ISI) of 0 minutes
Priming cTBS, followed by iTBS after an ISI of 0 minutes
Priming cTBS, followed by iTBS after an ISI of 10 minutes
Priming cTBS, followed by iTBS after an ISI of 20 minutes
Outcomes
Primary Outcome Measures
Change in hemoglobin concentrations (Hb) during rest
Oxy- and deoxy-hemoglobin (HbO, HHb) and total Hb will be acquired using functional near-infrared spectroscopy (fNIRS)
Change in hemoglobin concentrations (Hb) while participants perform an emotion stroop task and verbal fluency task
Oxy- and deoxy-hemoglobin (HbO, HHb) and total Hb will be acquired using functional near-infrared spectroscopy (fNIRS)
Secondary Outcome Measures
Change in reaction time during emotion stroop task
Before and after stimulation, participants will perform a emotion stroop task. Participants are asked to indicate by button press in which color (red, yellow, blue, green) the word is presented on a computer screen,("c" for red, "v" for yellow, "n" for blue, "m" for green) . The total number and the reaction time of correct response will be recorded.
Change in the number of correctly responded colored words in the emotional Stroop task and correctly generated words in the verbal fluency task.
Before and after stimulation, participants will perform an emotional Stroop task as described in Outcome 3. In addition, participants will also perform a verbal fluency task, In this task, participants are required to speak out as many unique words as possible during the word generation blocks, according to a given category (for example, name animals). The category will be presented at the center of the screen. The total number of correct answers will be recorded
Change in the number of correctly recognized emotion
In addition, participants will perform an emotion-recognition accuracy task. They will be presented with 64 facial stimuli, consisting of sets of 16 sad, happy, fearful and neutral faces, in a randomized order. Faces will be presented for a maximum of 6s. Participants have to indicate the depicted emotion by button press (choice between 4 answers) within the presentation period.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04031105
Brief Title
Probing Homeostatic Plasticity With Priming Theta-burst Stimulation of the Dorsolateral Prefrontal Cortex
Official Title
Probing Homeostatic Plasticity With Priming Theta-burst Stimulation of the Dorsolateral Prefrontal Cortex
Study Type
Interventional
2. Study Status
Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 23, 2021 (Actual)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Dr Georg Kranz
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Priming stimulation is a highly promising tool to boost the beneficial effects of therapeutic repetitive transcranial magnetic stimulation (rTMS) in psychiatry. The potentiating effects of priming stimulation, however, depend on the time interval between the priming and the test stimulation. Although it is known that too short and too long intervals have no effects, systematic studies that identify the time needed to maximize efficacy have not yet been done. Thus, there is a need for studies to investigate the effects of priming stimulation in order to fully utilize the potential benefits and advantages of this promising new rTMS protocol. This study will systematically investigate the neuromodulatory process underlying priming stimulation to enhance metaplasticity in the left dorsolateral prefrontal cortex (DLPFC) - one of the main targets for therapeutic rTMS - in individuals with subclinical depression.
The brain is a highly plastic organ and its activity can be influenced using rTMS. At the same time, the brain also has a mechanism - called homeostatic metaplasticity - which counteracts extreme plastic changes. Homeostatic metaplasticity therefore can limit the beneficial effects of brain stimulation interventions. However, priming stimulation protocols that include both a priming and a test stimulation session may utilize homeostatic metaplasticity to increase the beneficial effects of brain stimulation, although the optimal treatment parameters for priming are not known. Moreover, little is known about homeostatic metaplasticity in the DLPFC, an area that is particularly relevant for psychiatric conditions given its role in the top-down control of emotions. Here, the investigators will systematically study metaplasticity using priming theta-burst stimulation (TBS), a potent form of rTMS in the left DLPFC. Changes in blood oxygenation that signal brain activity changes will be assessed using functional near-infrared spectroscopy (fNIRS) at rest and during engagement in several cognitive tasks. The findings from this study will (1) elucidate the optimal time interval between priming and test stimulation; (2) elucidate the influence of priming TBS on emotion discrimination as well as executive function and its underlying brain activity in subclinical depression; and (3) validate homeostatic metaplasticity in the left DLPFC.
Detailed Description
No detailed description
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression Minor
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized, single blind, parallel group experiment
Masking
Participant
Masking Description
Participants will not be told which arm they belong to
Allocation
Randomized
Enrollment
80 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Condition 1
Arm Type
Experimental
Arm Description
Priming sham TBS, followed by iTBS after an inter-stimulation-interval (ISI) of 0 minutes
Arm Title
Condition 2
Arm Type
Experimental
Arm Description
Priming cTBS, followed by iTBS after an ISI of 0 minutes
Arm Title
Condition 3
Arm Type
Experimental
Arm Description
Priming cTBS, followed by iTBS after an ISI of 10 minutes
Arm Title
Condition 4
Arm Type
Experimental
Arm Description
Priming cTBS, followed by iTBS after an ISI of 20 minutes
Intervention Type
Device
Intervention Name(s)
Theta-burst stimulation (TBS)
Other Intervention Name(s)
Transcranial Magnetic Stimulation
Intervention Description
intermittent (iTBS) and continuous (cTBS) will be applied at an intensity of 70% or 100%* resting motor threshold (RMT) on the dorsolateral prefrontal cortex, position F3 (EEG 10-20 international system)
*The optimal %RMT will be evaluated in a pilot study before commencement of the main study
Primary Outcome Measure Information:
Title
Change in hemoglobin concentrations (Hb) during rest
Description
Oxy- and deoxy-hemoglobin (HbO, HHb) and total Hb will be acquired using functional near-infrared spectroscopy (fNIRS)
Time Frame
Change from baseline Hb at 15 minutes post-stimulation
Title
Change in hemoglobin concentrations (Hb) while participants perform an emotion stroop task and verbal fluency task
Description
Oxy- and deoxy-hemoglobin (HbO, HHb) and total Hb will be acquired using functional near-infrared spectroscopy (fNIRS)
Time Frame
Change from baseline Hb at 15 minutes after stimulation
Secondary Outcome Measure Information:
Title
Change in reaction time during emotion stroop task
Description
Before and after stimulation, participants will perform a emotion stroop task. Participants are asked to indicate by button press in which color (red, yellow, blue, green) the word is presented on a computer screen,("c" for red, "v" for yellow, "n" for blue, "m" for green) . The total number and the reaction time of correct response will be recorded.
Time Frame
Change from baseline reaction times at 15 minutes after stimulation
Title
Change in the number of correctly responded colored words in the emotional Stroop task and correctly generated words in the verbal fluency task.
Description
Before and after stimulation, participants will perform an emotional Stroop task as described in Outcome 3. In addition, participants will also perform a verbal fluency task, In this task, participants are required to speak out as many unique words as possible during the word generation blocks, according to a given category (for example, name animals). The category will be presented at the center of the screen. The total number of correct answers will be recorded
Time Frame
Change from baseline score at 15 minutes after stimulation
Title
Change in the number of correctly recognized emotion
Description
In addition, participants will perform an emotion-recognition accuracy task. They will be presented with 64 facial stimuli, consisting of sets of 16 sad, happy, fearful and neutral faces, in a randomized order. Faces will be presented for a maximum of 6s. Participants have to indicate the depicted emotion by button press (choice between 4 answers) within the presentation period.
Time Frame
Change from baseline score at 15 minutes after stimulation
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
age 18-35
education level of primary six or above
right-handedness
normal or corrected-to-normal vision
being able to understand the verbal instructions
willingness to sign the informed consent form
Exclusion Criteria:
a history of seizures
current or past psychiatric disorders
current or past severe internal or neurological illness
ferromagnetic implants <20cm from the head, cardiac pacemaker, deep brain stimulation and other common TMS exclusion criteria
history of substance dependence or abuse within the last 3 months
intake of any medication known to affect the excitation threshold (i.e., benzodiazepines, anticonvulsants).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Georg S Kranz, PhD
Phone
2766
Ext
4838
Email
georg.kranz@polyu.edu.hk
First Name & Middle Initial & Last Name or Official Title & Degree
Bingbing B Zhang, MSc
Phone
2766
Ext
4838
Email
bellabingbing.zhang@connect.polyu.hk
Facility Information:
Facility Name
The Hong Kong Polytechnic University
City
Hong Kong
Country
Hong Kong
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Georg S Kranz, PhD
Phone
2766
Ext
4838
Email
georg.kranz@polyu.edu.hk
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
Sharing upon request
Learn more about this trial
Probing Homeostatic Plasticity With Priming Theta-burst Stimulation of the Dorsolateral Prefrontal Cortex
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