search
Back to results

Neuronavigation rTMS to Improve Depressive Episodes of Bipolar Disorder in Adolescent

Primary Purpose

Bipolar Disorder

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Repetitive Transcranial magnetic stimulation
Sham Repetitive Transcranial magnetic stimulation
Sponsored by
First Affiliated Hospital of Zhejiang University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bipolar Disorder

Eligibility Criteria

14 Years - 28 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Age 14-28 years old, regardless of gender; Meet DSM-V diagnostic criteria for bipolar depressive episodes; Young Mania Rating Scale (YMRS) ≤ 6 points; MARDS:12-30 points. Han nationality, right-handed; More than 9 years of education. Exclusion Criteria: History of severe somatic or brain organic diseases and craniocerebral trauma; Abnormal brain structure or any MRI contraindications were found by magnetic resonance examination; Those who do not cooperate or cannot effectively complete the experiment; Drug, alcohol or other psychoactive substance abusers; Pregnant, lactating or planned pregnancy. Severe suicidal ideation and behavior ECT or rTMS treatment was performed within six months

Sites / Locations

  • The First Affiliated Hospital of Zhejiang University

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Sham Comparator

Arm Label

Repetitive Transcranial magnetic stimulation

Sham Repetitive Transcranial magnetic stimulation

Arm Description

Outcomes

Primary Outcome Measures

Montgomery-Asberg Depression Rating Scale(MADRS)
Montgomery-Asberg Depression Rating Scale (MADRS) is used to reflect the effect of antidepressant treatment and monitor the change of patients' condition. The scale is a separate scale, and the score should be based on clinical interviews. The symptoms should be asked from broad to detailed, so as to accurately score the severity. The rater must determine whether the score is on the defined score values (0,2,4,6) or between these scores (1,3,5), according to clinical practice. The scale can be used to score at any time interval.

Secondary Outcome Measures

Full Information

First Posted
June 26, 2023
Last Updated
September 12, 2023
Sponsor
First Affiliated Hospital of Zhejiang University
search

1. Study Identification

Unique Protocol Identification Number
NCT05929183
Brief Title
Neuronavigation rTMS to Improve Depressive Episodes of Bipolar Disorder in Adolescent
Official Title
Efficacy and Safety Study of Neuronavigation Occipital rTMS to Improve Depressive Episodes of Bipolar Disorder in Adolescent
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Completed
Study Start Date
September 1, 2022 (Actual)
Primary Completion Date
June 30, 2023 (Actual)
Study Completion Date
July 1, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
First Affiliated Hospital of Zhejiang University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The purpose of this study is to explore a new stimulation target and protocol for the treatment of depressive episode in adolescents with bipolar disorder through the repetitive transcranial magnetic stimulation(rTMS) under neuronavigation, and verify whether there is abnormal functional connectivity between the emotion-related brain area orbital frontal lobe (OFC) and the primary visual cortex(V1) during the depressive episode, which will contribute to further understand the relevant neural pathway and mechanism.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bipolar Disorder

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Repetitive Transcranial magnetic stimulation
Arm Type
Active Comparator
Arm Title
Sham Repetitive Transcranial magnetic stimulation
Arm Type
Sham Comparator
Intervention Type
Device
Intervention Name(s)
Repetitive Transcranial magnetic stimulation
Intervention Description
Setting up a new target for rTMS. In the past research, the common target of rTMS in the treatment of depressive symptom was dorsolateral prefrontal cortex (DLPFC). In this study, we use high frequency rTMS in the occipital lobe are precisely targeted by navigation, by stimulating the primary visual cortex(V1), can affect the orbitofrontal cortex (OFC), which is functionally connected to V1, and thus affect the entire nerve ring pathway excitability, thereby rapidly, effectively and safely improving mood symptoms in the acute phase of bipolar depressive episode. After the target was determined by fMRI navigation and positioning, the subjects were subjected to rTMS for 20 minutes per day with the stimulation intensity of 10Hz and 100% of the motion threshold(MT),stimulation time of each sequence was 5 seconds, stimulation interval was 15 seconds, 3000 pulses per day for 15 days, and the total number of pulses was 45000.
Intervention Type
Device
Intervention Name(s)
Sham Repetitive Transcranial magnetic stimulation
Intervention Description
The stimulus intensity was 20% of MT in the Sham Comparator arm, and the remaining parameters were the same as the Active Comparator arm.
Primary Outcome Measure Information:
Title
Montgomery-Asberg Depression Rating Scale(MADRS)
Description
Montgomery-Asberg Depression Rating Scale (MADRS) is used to reflect the effect of antidepressant treatment and monitor the change of patients' condition. The scale is a separate scale, and the score should be based on clinical interviews. The symptoms should be asked from broad to detailed, so as to accurately score the severity. The rater must determine whether the score is on the defined score values (0,2,4,6) or between these scores (1,3,5), according to clinical practice. The scale can be used to score at any time interval.
Time Frame
0-8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
14 Years
Maximum Age & Unit of Time
28 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 14-28 years old, regardless of gender; Meet DSM-V diagnostic criteria for bipolar depressive episodes; Young Mania Rating Scale (YMRS) ≤ 6 points; MARDS:12-30 points. Han nationality, right-handed; More than 9 years of education. Exclusion Criteria: History of severe somatic or brain organic diseases and craniocerebral trauma; Abnormal brain structure or any MRI contraindications were found by magnetic resonance examination; Those who do not cooperate or cannot effectively complete the experiment; Drug, alcohol or other psychoactive substance abusers; Pregnant, lactating or planned pregnancy. Severe suicidal ideation and behavior ECT or rTMS treatment was performed within six months
Facility Information:
Facility Name
The First Affiliated Hospital of Zhejiang University
City
Hangzhou
State/Province
Zhejiang
ZIP/Postal Code
310000
Country
China

12. IPD Sharing Statement

Learn more about this trial

Neuronavigation rTMS to Improve Depressive Episodes of Bipolar Disorder in Adolescent

We'll reach out to this number within 24 hrs