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A Multicenter Randomized Controlled Study of Pulse Magnetotherapy Combined Medication in Anxiety Combined With Insomnia

Primary Purpose

Anxiety Disorder, Insomnia

Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Pulse magnetic therapy
Selective serotonin reuptake inhibitors (SSRI)
Shame magnetic therapy
Sponsored by
Second Affiliated Hospital, School of Medicine, Zhejiang University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anxiety Disorder focused on measuring Anxiety, Insomnia, Pulse Magnetotherapy

Eligibility Criteria

18 Years - 55 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Patients who met the diagnostic criteria for anxiety disorder in the Diagnostic and Statistical Manual of Mental Disorders (Fifth edition; DSM-5) and were accompanied by insomnia with 14 <HAMA<21 , HAMD<17 , and PSQI>7 ; Education level is unlimited; Age: 18-55 years old. Exclusion Criteria: Have bipolar disorder, schizophrenia, depression and other mental diseases; Have a clear history of head trauma, alcoholism, brain tumors, diabetes, hypertension, and serious primary heart, liver, kidney, and blood system diseases; At present, patients with sleep disorders are being treated by other means besides drugs; Pregnant and lactating women; Have a history of seizures or strong positive family history of epilepsy; Implantation of cardiac pacemaker; Those receiving deep brain stimulation treatment; There are metal or magnetic implants in the body (including but not limited to the brain); Participated in clinical trials of other drugs and medical devices in recent 3 months; Other researchers believe that they do not meet the conditions for inclusion.

Sites / Locations

  • Changxing County People's HospitaRecruiting
  • Linping First People's HospitalRecruiting
  • The Fourth Affiliated Hospital of Zhejiang University School of medicineRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Sham Comparator

Other

Arm Label

Pulse Magnetotherapy+medication group

medication group

Healthy control

Arm Description

150 patients with anxiety disorder and insomnia who met the inclusion criteria received pulse magnetic therapy and conventional antianxiety drugs

150 patients with anxiety disorder and insomnia who met the inclusion criteria received sham magnetic therapy and conventional antianxiety drugs

100 healthy controls who met the inclusion criteria received sham magnetic therapy

Outcomes

Primary Outcome Measures

Insomnia Severity Index (ISI)
Insomnia Severity Index total score reduction>50%, the range of Insomnia Severity Index total score is 0-28.

Secondary Outcome Measures

Full Information

First Posted
October 25, 2022
Last Updated
February 15, 2023
Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University
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1. Study Identification

Unique Protocol Identification Number
NCT05705830
Brief Title
A Multicenter Randomized Controlled Study of Pulse Magnetotherapy Combined Medication in Anxiety Combined With Insomnia
Official Title
A Multicenter Randomized Controlled Study of Pulse Magnetotherapy Combined Medication in the Treatment of Patients With Anxiety Disorder and Insomnia
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
November 1, 2022 (Actual)
Primary Completion Date
November 30, 2025 (Anticipated)
Study Completion Date
December 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No

5. Study Description

Brief Summary
The goal of this clinical trial is to explore the therapeutic effect of pulse magnetic therapy system combined with drug therapy on patients with anxiety and insomnia. The main questions it aims to answer are: Whether the pulse magnetic therapy system is benefit on improving insomnia in anxiety patients. This improvement is not due to the placement of the instrument。 Participants will accept pulse magnetic therapy (stimulation/sham stimulation) and accept scale evaluation before and after treatment. Researchers will compare the pulse magnetic stimulation group, sham stimulation group and healthy controls to see if the pulse magnetic stimulation do effect on insomnia of anxiety patients.
Detailed Description
Insomnia is the most common symptom of anxiety disorder, which has an important impact on the prognosis of anxiety. Pulse magnetic therapy system, with its advantages of compact, convenient, easy to carry, and not limited by the scene and time, has gradually become a common tool for sleep monitoring and treatment. This study is a multicenter randomized controlled design, including 150 cases in the pulse magnetic stimulation+drug treatment group, 150 cases in the sham pulse magnetic stimulation+drug treatment group and 100 healthy controls. Before and after treatment, the patients were comprehensively measured and evaluated with Insomnia Severity Index (ISI), Hamilton Depression Rating Scale 17 (HAMD), Hamilton Anxiety Rating Scale (HAMA), Pittsburgh Sleep Quality Index (PSQI), Self-Rating Sleep Scale (SSRS), Self-Rating Symptom Scale 90 (SCL-90), Quality of Life Scale (SF-36), and Treatment Adverse Reaction Scale (TESS), and sleep monitoring was conducted at the same time, To explore the therapeutic effect of pulse magnetic therapy system detector combined with drug therapy on patients with anxiety and insomnia.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anxiety Disorder, Insomnia
Keywords
Anxiety, Insomnia, Pulse Magnetotherapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
400 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Pulse Magnetotherapy+medication group
Arm Type
Experimental
Arm Description
150 patients with anxiety disorder and insomnia who met the inclusion criteria received pulse magnetic therapy and conventional antianxiety drugs
Arm Title
medication group
Arm Type
Sham Comparator
Arm Description
150 patients with anxiety disorder and insomnia who met the inclusion criteria received sham magnetic therapy and conventional antianxiety drugs
Arm Title
Healthy control
Arm Type
Other
Arm Description
100 healthy controls who met the inclusion criteria received sham magnetic therapy
Intervention Type
Device
Intervention Name(s)
Pulse magnetic therapy
Intervention Description
Pulse magnetic therapy SM-II (2019102133903)
Intervention Type
Drug
Intervention Name(s)
Selective serotonin reuptake inhibitors (SSRI)
Intervention Description
Anti-anxiety Drugs
Intervention Type
Device
Intervention Name(s)
Shame magnetic therapy
Intervention Description
Shame magnetic therapy
Primary Outcome Measure Information:
Title
Insomnia Severity Index (ISI)
Description
Insomnia Severity Index total score reduction>50%, the range of Insomnia Severity Index total score is 0-28.
Time Frame
Change value of insomnia severity index (ISI) from baseline in the fourth week of intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patients who met the diagnostic criteria for anxiety disorder in the Diagnostic and Statistical Manual of Mental Disorders (Fifth edition; DSM-5) and were accompanied by insomnia with 14 <HAMA<21 , HAMD<17 , and PSQI>7 ; Education level is unlimited; Age: 18-55 years old. Exclusion Criteria: Have bipolar disorder, schizophrenia, depression and other mental diseases; Have a clear history of head trauma, alcoholism, brain tumors, diabetes, hypertension, and serious primary heart, liver, kidney, and blood system diseases; At present, patients with sleep disorders are being treated by other means besides drugs; Pregnant and lactating women; Have a history of seizures or strong positive family history of epilepsy; Implantation of cardiac pacemaker; Those receiving deep brain stimulation treatment; There are metal or magnetic implants in the body (including but not limited to the brain); Participated in clinical trials of other drugs and medical devices in recent 3 months; Other researchers believe that they do not meet the conditions for inclusion.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Zheng Lin, Doctor
Phone
86-13757118261
Email
Linzzr@126.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zheng Lin
Organizational Affiliation
Second Affiliated Hospital, School of Medicine, Zhejiang University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Changxing County People's Hospita
City
Changxing
State/Province
Zhejiang
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tao Yan, Master
Phone
86-13957258775
Facility Name
Linping First People's Hospital
City
Linping
State/Province
Zhejiang
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yuze Sheng, Master
Phone
86-15990077882
Facility Name
The Fourth Affiliated Hospital of Zhejiang University School of medicine
City
Yiwu
State/Province
Zhejiang
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yunrong Lu, Doctor
Phone
86-13757118257

12. IPD Sharing Statement

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A Multicenter Randomized Controlled Study of Pulse Magnetotherapy Combined Medication in Anxiety Combined With Insomnia

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