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Functional Near-infrared Spectroscopy for Anxiety Monitoring and Neurofeedback.

Primary Purpose

Anxiety Disorders

Status
Recruiting
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
AI-fNIRS neurofeedback device
AI-fNIRS neurofeedback device with sham signals
Sponsored by
National Taiwan University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anxiety Disorders

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Being diagnosed with generalized anxiety disorder (GAD) by psychiatrists based on DSM-V. Native Chinese speakers. Right-handers. Normal vision without or after correction. Normal hearing and verbal expression. Regular returns of medical or psychological intervention during participation. Exclusion Criteria: Being diagnosed with other major neurological or mental disorders.

Sites / Locations

  • National Taiwan University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

GAD Patients with Intervention

GAD Patients with Sham Controls

Arm Description

The feedback group will get real neurofeedback about changes in anxiety-related cerebral hemodynamics. AI-fNIRS neurofeedback will be provided 3 times a week, for a total of 4 weeks.

The sham group will be shown playbacks of someone's real feedback sessions. Sham AI-fNIRS neurofeedback will be provided 3 times a week, for a total of 4 weeks.

Outcomes

Primary Outcome Measures

Change in cerebral hemodynamics from functional near-infrared spectroscopy (fNIRS)
fNIRS is an optical brain monitoring technique. It serves as an ideal tool to record brain activities based on hemodynamics during various cognitive or motor tasks. The regions of interest are bihemispheric prefrontal cortices.
Change in severity of physiological and psychological anxious symptoms as assessed by Hamilton Anxiety Rating Scale (HARS)
Hamilton Anxiety Rating Scale (HARS) is a frequently-used scale in clinical psychiatric fields to assess the severity of anxious symptoms. Conducted by well-trained clinicians, HARS consists of 14 items and can be classified into 2 domains: physiological and psychological anxious symptoms. The minimum and maximum values are 0 and 56 respectively, with higher scores represent worse outcomes.
Change in temporary and long-term anxiety levels as assessed by State-Trait Anxiety Inventory (STAI)
State-Trait Anxiety Inventory (STAI) is a self-report measure of subjective feelings of anxiety. It consists of 2 subscales: state and trait anxiety, with the former characteristic of temporary states of emotion and the latter dealing with the frequency of anxiety and other related emotion in general conditions. The minimum and maximum values of each subscale are 20 and 80 respectively. The higher the score, the higher the level of anxiety.
Change in anxiety level as reported in Visual Analog Scale (VAS)
VAS is a self-report measure. Participants are required to draw a 10 cm line representing their anxiety spectrum, and mark their subjective feelings of anxiety level on it, with the highest on the right end.
Change in physiological anxious symptoms indicated by Heart Rate Variability (HRV)
Measured with Apple Watch, HRV serves as a physiological index of anxiety. Subjects with anxiety will show lower HRV than healthy individuals.

Secondary Outcome Measures

Change in performance on Emotional Stroop Task
Sixty words related to either positive, neutral or negative emotion are displayed in various colors in the emotional Stroop task. Participants are required to read out the color of each word as accurately and quickly as possible. The differences in reaction rate between negative emotion and the two other conditions indicate to what extent participants are affected by emotion.
Change in performance on Dot-Probe Task
Two images are first displayed on the left and right sides respectively and randomly, with one related to negative emotion and another related to neutral emotion. After the images disappear, a dot pops up on either side at random. Participants are required to indicate the direction where the dot showing up by pressing the button as soon as possible. The difference in reaction rate between the negative and neutral emotional images represents the extent to which the participants are influenced by emotion.
Change in Pittsburgh Sleep Quality Index (PSQI)
PSQI is a self-report measure of sleep quality. It consists of 9 items and is related to 7 dimensions of sleep. The higher the score is, the worse the quality of sleep.
Change in concentration of brain-derived neurotrophic factor (BDNF)
BDNF, a protein of the highest content in the brain, promotes neuron growth and synapse formation. Its secretion is inhibited under stress or depression; accordingly, BDNF serves as a biological index of aforementioned conditions.
Change in concentration of Interleukin-6 (IL-6)
IL-6 is a proinflammatory cytokine and capable of modulating immune and inflammatory response. The level of IL-6 is elevated under stress, depression, etc. and hence serves as an indicator of such conditions.

Full Information

First Posted
June 13, 2023
Last Updated
June 26, 2023
Sponsor
National Taiwan University Hospital
Collaborators
National Science Council, Taiwan
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1. Study Identification

Unique Protocol Identification Number
NCT05921773
Brief Title
Functional Near-infrared Spectroscopy for Anxiety Monitoring and Neurofeedback.
Official Title
Clinical Evaluation of Functional Near-infrared Spectroscopy for Anxiety Monitoring and Neurofeedback.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 1, 2023 (Actual)
Primary Completion Date
April 30, 2027 (Anticipated)
Study Completion Date
April 30, 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Taiwan University Hospital
Collaborators
National Science Council, Taiwan

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
The objective of this subproject is to validate the efficacy of the fNIRS real-time anxiety monitoring and neurofeedback system. In the first year, the cerebral hemodynamics measured by commercial fNIRS during resting state and cognitive tasks from 60 generalized anxiety disorder (GAD) patients and 30 healthy subjects will be processed and analyzed using AI algorithms. The novel anxiety fNIRS biomarker will be identified and correlated to clinical anxiety scales (such as HARS and STAI). In the second year, the reliability, validity, and responsiveness of the AI-fNIRS biomarker will be validated. The accuracy of using AI-fNIRS biomarker to predict the diagnosis of GAD (according to DSM-5) and anxiety rating scales will be calculated from 60 GAD patients and 30 healthy subjects. In the third year, a neurofeedback method using AI-fNIRS biomarkers to guide digital cognitive behavior therapy (dCBT) through visual/audio cues will be developed. A pilot study with 12 GAD patients will be performed to test the feasibility of mindfulness training during AI-fNIRS neurofeedback. In the fourth year, a large scale RCT will be performed to validate the therapeutic efficacy of AI-fNIRS neurofeedback dCBT in 40 patients with GAD. The protocol of using real-time AI-fNIRS biomarkers as a neurofeedback to augment mindfulness training will be optimized according to previous year.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anxiety Disorders

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
232 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
GAD Patients with Intervention
Arm Type
Experimental
Arm Description
The feedback group will get real neurofeedback about changes in anxiety-related cerebral hemodynamics. AI-fNIRS neurofeedback will be provided 3 times a week, for a total of 4 weeks.
Arm Title
GAD Patients with Sham Controls
Arm Type
Sham Comparator
Arm Description
The sham group will be shown playbacks of someone's real feedback sessions. Sham AI-fNIRS neurofeedback will be provided 3 times a week, for a total of 4 weeks.
Intervention Type
Device
Intervention Name(s)
AI-fNIRS neurofeedback device
Intervention Description
The device, with AI-fNIRS signals serving as brain monitor to indicate the level of anxiety, provides mindfulness training through visual and auditory cues to help participants modulate their brain activity, and thus alleviates anxious states.
Intervention Type
Device
Intervention Name(s)
AI-fNIRS neurofeedback device with sham signals
Intervention Description
The sham control consists of playbacks of someone else's real AI-fNIRS neurofeedback and will be provided 3 times a week, for a total of 4 weeks.
Primary Outcome Measure Information:
Title
Change in cerebral hemodynamics from functional near-infrared spectroscopy (fNIRS)
Description
fNIRS is an optical brain monitoring technique. It serves as an ideal tool to record brain activities based on hemodynamics during various cognitive or motor tasks. The regions of interest are bihemispheric prefrontal cortices.
Time Frame
Baseline, 4-week intervention, and 2 months after 4-week intervention.
Title
Change in severity of physiological and psychological anxious symptoms as assessed by Hamilton Anxiety Rating Scale (HARS)
Description
Hamilton Anxiety Rating Scale (HARS) is a frequently-used scale in clinical psychiatric fields to assess the severity of anxious symptoms. Conducted by well-trained clinicians, HARS consists of 14 items and can be classified into 2 domains: physiological and psychological anxious symptoms. The minimum and maximum values are 0 and 56 respectively, with higher scores represent worse outcomes.
Time Frame
Baseline, 4-week intervention, and 2 months after 4-week intervention.
Title
Change in temporary and long-term anxiety levels as assessed by State-Trait Anxiety Inventory (STAI)
Description
State-Trait Anxiety Inventory (STAI) is a self-report measure of subjective feelings of anxiety. It consists of 2 subscales: state and trait anxiety, with the former characteristic of temporary states of emotion and the latter dealing with the frequency of anxiety and other related emotion in general conditions. The minimum and maximum values of each subscale are 20 and 80 respectively. The higher the score, the higher the level of anxiety.
Time Frame
Baseline, 4-week intervention, and 2 months after 4-week intervention.
Title
Change in anxiety level as reported in Visual Analog Scale (VAS)
Description
VAS is a self-report measure. Participants are required to draw a 10 cm line representing their anxiety spectrum, and mark their subjective feelings of anxiety level on it, with the highest on the right end.
Time Frame
Baseline, 4-week intervention, and 2 months after 4-week intervention.
Title
Change in physiological anxious symptoms indicated by Heart Rate Variability (HRV)
Description
Measured with Apple Watch, HRV serves as a physiological index of anxiety. Subjects with anxiety will show lower HRV than healthy individuals.
Time Frame
Baseline, 4-week intervention, and 2 months after 4-week intervention.
Secondary Outcome Measure Information:
Title
Change in performance on Emotional Stroop Task
Description
Sixty words related to either positive, neutral or negative emotion are displayed in various colors in the emotional Stroop task. Participants are required to read out the color of each word as accurately and quickly as possible. The differences in reaction rate between negative emotion and the two other conditions indicate to what extent participants are affected by emotion.
Time Frame
Baseline, 4-week intervention, and 2 months after 4-week intervention.
Title
Change in performance on Dot-Probe Task
Description
Two images are first displayed on the left and right sides respectively and randomly, with one related to negative emotion and another related to neutral emotion. After the images disappear, a dot pops up on either side at random. Participants are required to indicate the direction where the dot showing up by pressing the button as soon as possible. The difference in reaction rate between the negative and neutral emotional images represents the extent to which the participants are influenced by emotion.
Time Frame
Baseline, 4-week intervention, and 2 months after 4-week intervention.
Title
Change in Pittsburgh Sleep Quality Index (PSQI)
Description
PSQI is a self-report measure of sleep quality. It consists of 9 items and is related to 7 dimensions of sleep. The higher the score is, the worse the quality of sleep.
Time Frame
Baseline, 4-week intervention, and 2 months after 4-week intervention.
Title
Change in concentration of brain-derived neurotrophic factor (BDNF)
Description
BDNF, a protein of the highest content in the brain, promotes neuron growth and synapse formation. Its secretion is inhibited under stress or depression; accordingly, BDNF serves as a biological index of aforementioned conditions.
Time Frame
Baseline, 4-week intervention, and 2 months after 4-week intervention.
Title
Change in concentration of Interleukin-6 (IL-6)
Description
IL-6 is a proinflammatory cytokine and capable of modulating immune and inflammatory response. The level of IL-6 is elevated under stress, depression, etc. and hence serves as an indicator of such conditions.
Time Frame
Baseline, 4-week intervention, and 2 months after 4-week intervention.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Being diagnosed with generalized anxiety disorder (GAD) by psychiatrists based on DSM-V. Native Chinese speakers. Right-handers. Normal vision without or after correction. Normal hearing and verbal expression. Regular returns of medical or psychological intervention during participation. Exclusion Criteria: Being diagnosed with other major neurological or mental disorders.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yi-Jing Huang, Assistant Professor
Phone
+886911164386
Email
yijinghuang@ntu.edu.tw
Facility Information:
Facility Name
National Taiwan University Hospital
City
Taipei
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yi-Jing Huang, Assistant Professor
Phone
+886911164386
Email
yijinghuang@ntu.edu.tw

12. IPD Sharing Statement

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Functional Near-infrared Spectroscopy for Anxiety Monitoring and Neurofeedback.

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