Study on the Mode and Mechanism of Ultra-low Frequency rTMS for Sleep Disorders in Patients With Parkinson's Disease

Sponsor
Qianfoshan Hospital (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT04804176
Collaborator
(none)
99
1
3
28
3.5

Study Details

Study Description

Brief Summary

The study by giving a sleep disorder Parkinson's disease patients with different patterns of ultra-low frequency transcranial magnetic stimulation or sham stimulation, scale for assessment of the patients were observed, hematology and imaging changes before and after therapy, clear ultra-low frequency transcranial magnetic stimulation for sleep disorder Parkinson's disease treatment, to explore the mechanism of action, compare the difference between different modes.

Condition or Disease Intervention/Treatment Phase
  • Device: Ultra-low frequency repetitive transcranial magnetic stimulation
N/A

Detailed Description

Parkinson's disease is the second most common chronic neurodegenerative disease.At present, researchers focus not only on the motor symptoms of Parkinson's disease, but also on the non-motor symptoms of Parkinson's disease (including mood disorders, sleep disorders, cognitive decline, and autonomic nervous kinetic disorder, etc.).The principle of transcranial magnetic stimulation is based on the electromagnetic principle proposed by Faraday. When an electrifying coil is suspended over the scalp at a certain distance, the magnetic field generated by the coil current and the electric field generated by the magnetic field can reach the skull and directly or indirectly affect the synapses and neurons in the brain.The study by giving a sleep disorder Parkinson's disease patients with different patterns of ultra-low frequency transcranial magnetic stimulation or sham stimulation, scale for assessment of the patients were observed, hematology and imaging changes before and after therapy, clear ultra-low frequency transcranial magnetic stimulation for sleep disorder Parkinson's disease treatment, to explore the mechanism of action, compare the difference between different modes.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
99 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
The study was divided into three groups, which were control group, group A and group B.Groups A and B received different treatment modalities on the same device.The study was divided into three groups, which were control group, group A and group B.Groups A and B received different treatment modalities on the same device.
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Study on the Mode and Mechanism of Ultra-low Frequency Repetitive Transcranial Magnetic Stimulation for Sleep Disorders in Patients With Parkinson's Disease
Actual Study Start Date :
Dec 20, 2019
Anticipated Primary Completion Date :
Dec 20, 2021
Anticipated Study Completion Date :
Apr 20, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: 5-HT mode of Ultra-low frequency repetitive transcranial magnetic stimulation

The study used 5-HT mode of Ultra-low frequency repetitive transcranial magnetic stimulation for 35 minutes once a day.Every 7 days is a cycle.The stimulus intensity was 400GS.

Device: Ultra-low frequency repetitive transcranial magnetic stimulation
Two different modes of the instrument were used to treat patients in groups, to compare the efficacy.

Active Comparator: GABA mode of ultra-low frequency repetitive transcranial magnetic stimulation

The study used GABA mode of ultra-low frequency repetitive transcranial magnetic stimulation for 35 minutes once a day.Every 7 days is a cycle.The stimulus intensity was 400GS

Device: Ultra-low frequency repetitive transcranial magnetic stimulation
Two different modes of the instrument were used to treat patients in groups, to compare the efficacy.

Sham Comparator: the control group

The instrument is not working, only in exhaust mode.

Device: Ultra-low frequency repetitive transcranial magnetic stimulation
Two different modes of the instrument were used to treat patients in groups, to compare the efficacy.

Outcome Measures

Primary Outcome Measures

  1. change from length of sleep at one week [one week]

    Sleep duration was monitored by polysomnography.It's measured in minutes.

  2. change from ratio of stage 3 sleep in total sleep at one week [one week]

    The proportion of phase 3 sleep in total sleep was monitored by polysomnography.It's in percentages.

  3. change from limb movement of sleep at one week [one week]

    The number of body movements during sleep was recorded by polysomnography.It's in units of times per night.

  4. change from nocturnal arousal frequency at one week [one week]

    The number of nocturnal awakenings was recorded by polysomnography.It's in units of times per night.

  5. change from Pittsburgh sleep quality index scale at one week [1 day before treatment、1 day after treatment、1 week after treatment、1 moth after treatment]

    The scale was evaluated on the day before treatment and the day after treatment, which was based on scores.The total score of the scale ranges from 0 to 2L, and the higher the score, the worse the sleep quality.

  6. Interleukin 6 [1 day before treatment and 1 day after treatment]

    It plays an important role in central nervous system diseases. In PD, the increase of IL-6 is the body's self-defense mechanism to protect neurons, and the change of IL-6 in peripheral blood can reflect the change of injury aggravation and recovery.It is also associated with psychiatric symptoms, and IL-6 is elevated in major depression.

  7. change from the Epworth sleepiness scale at one week [one week]

    The scale was evaluated on the day before treatment and the day after treatment, which was based on scores.The scale has an overall score range of 0 to 24, with higher scores indicating more severe sleepiness.

  8. change from Parkinson's disease sleep scale at one week [one week]

    The scale was evaluated on the day before treatment and the day after treatment, which was based on scores.The total score of the scale ranges from 0 to 150. The higher the score, the better the sleep.

  9. change from movement disorders association - comprehensive rating scale of Parkinson's disease at one week [one week]

    The scale was evaluated on the day before treatment and the day after treatment, which was based on scores.The total score of the scale ranged from 0 to 260, and the higher the score, the more severe the symptoms were.

  10. change from Parkinson's disease quality of life scale one week [one week]

    The scale was evaluated on the day before treatment and the day after treatment, which was based on scores.The total score of the scale ranges from 0 to 156, and the higher the score, the worse the quality of life.

  11. change from Hamilton depression scale at one week [one week]

    The scale was evaluated on the day before treatment and the day after treatment, which was based on scores.The total score of the scale ranged from 0 to 96, and the higher the score, the more severe the depression was.

  12. change from Hamilton anxiety scale at one week [one week]

    The scale was evaluated on the day before treatment and the day after treatment, which was based on scores.The total score of the scale ranges from 0 to 56, and the higher the score, the more serious the anxiety.

  13. change from simple mental state scale at one week [one week]

    The scale was evaluated on the day before treatment and the day after treatment, which was based on scores.The total score of the scale ranges from 0 to 30, and the lower the score, the more severe the cognitive impairment.

  14. change from Montreal cognitive assessment scale at one week [one week]

    The scale was evaluated on the day before treatment and the day after treatment, which was based on scores.The total score of the scale ranges from 0 to 30, and the lower the score, the more severe the cognitive impairment.

  15. change from magnetic resonance imaging of the brain at one month [one month]

    The ADC values of sleep-related brain tissues were measured by diffusion weighted magnetic resonance imaging of the brain.Compare the difference between the measured results on both sides of the same site and record the difference.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • in line with international Movement disorders association (the Movement Disorder Society, MDS) in 2015 the diagnosis of Parkinson's disease diagnosis standard and China standard (2016)

  • can cooperate to complete rating scale, the sleep monitoring, imaging and blood test

  • have a sleep disorder

  • aged 18 to 70 years old

  • agree to participate in this experiment, and have signed the informed consent

Exclusion Criteria:
  • superposition of diagnosed with Parkinson's syndrome

  • secondary diagnosed Parkinson's syndrome

  • is equipped with heart pacemakers and other metal implants

  • cannot achieve scale assessment

  • has significant malignant diseases

  • has a history of seizures

Contacts and Locations

Locations

Site City State Country Postal Code
1 The First Affiliated Hospital of Shandong First Medical University Jinan Shandong China

Sponsors and Collaborators

  • Qianfoshan Hospital

Investigators

  • Principal Investigator: Xiuhua Li, MD, Qianfoshan Hospital,The First Affiliated Hospital of Shandong First Medical University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Lili Cao, Professor, Qianfoshan Hospital
ClinicalTrials.gov Identifier:
NCT04804176
Other Study ID Numbers:
  • ULFRTMS-S
First Posted:
Mar 18, 2021
Last Update Posted:
Mar 24, 2021
Last Verified:
Mar 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
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
Keywords provided by Lili Cao, Professor, Qianfoshan Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 24, 2021