PET/MRI Study on the Neurological Mechanism of rTMS Treatment for Heroin Addiction

Sponsor
Tang-Du Hospital (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT04086459
Collaborator
(none)
90
1
3
37
2.4

Study Details

Study Description

Brief Summary

Heroin addiction is a serious problem and the relapse rate of existing treatment methods is extremely high. Recently, international journals such as Science reported that repetitive transcranial magnetic stimulation (rTMS) can reduce the craving of addicts, alleviate depression and anxiety symptoms, and is expected to become an effective treatment. Our preliminary experiment using rTMS to stimulate the left dorsolateral prefrontal cortex of heroin addicts also showed similar effects, however, the mechanism is unclear. Previously, the investigators found that the functional connectivity between left executive control network and default mode network was negatively correlated relapse behavior, while the functional connectivity between salience network and default mode network was positively correlated with relapse behavior. Studies have shown that dopamine dysfunction in addicts and brain metabolism is the biological basis of network connectivity. It suggests that elucidating the relationship between the characteristics of large brain network connectivity and the level of dopamine receptor and relapse behavior in addicts is hopeful to further understand the neurological mechanism of rTMS treatment for addiction. In this project, the investigators intend to observe the changes of brain network connectivity, glucose metabolism and dopamine D2 receptor before and after rTMS treatment in addicts from the perspective of large brain network by combining PET/MRI with psychobehavioral approach. The relationship between rTMS and relapse behavior will be deeply analyzed to provide scientific basis for the development of effective treatment programs.

Condition or Disease Intervention/Treatment Phase
  • Device: Repetitive transcranial magnetic stimulation
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
90 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Three groups (two groups of heroin addiction during methadone maintenance treatment and one healthy control group) were included in this study design. One heroin addiction group was administered active repetitive transcranial magnetic stimulation (rTMS) while another heroin addiction group was administered sham. The healthy control group was not given rTMS, just as control.Three groups (two groups of heroin addiction during methadone maintenance treatment and one healthy control group) were included in this study design. One heroin addiction group was administered active repetitive transcranial magnetic stimulation (rTMS) while another heroin addiction group was administered sham. The healthy control group was not given rTMS, just as control.
Masking:
Triple (Participant, Care Provider, Outcomes Assessor)
Masking Description:
Either the participants, care providers, or outcomes assessors did not know which repetitive transcranial magnetic stimulation is active or sham.
Primary Purpose:
Treatment
Official Title:
PET/MRI Study on the Neurological Mechanism of rTMS Treatment for Heroin Addiction by Stimulating Left Dorsolateral Prefrontal Cortex
Actual Study Start Date :
Jun 1, 2019
Anticipated Primary Completion Date :
Jul 1, 2021
Anticipated Study Completion Date :
Jul 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Active repetitive transcranial magnetic stimulation

Device: Repetitive transcranial magnetic stimulation
Those receiving experimental treatment will receive 20 sessions of rTMS, stimulation protocol included 20 sessions within 30 days (once a day, 5 days/week, 4 weeks, 10 Hz frequency, pulse intensity 100% of the resting motor threshold, 50 pulses per train, inter train pause of 10 s, 40 stimulation trains, 2000 pulses/ session)

Sham Comparator: Sham repetitive transcranial magnetic stimulation

Device: Repetitive transcranial magnetic stimulation
Those receiving experimental treatment will receive 20 sessions of rTMS, stimulation protocol included 20 sessions within 30 days (once a day, 5 days/week, 4 weeks, 10 Hz frequency, pulse intensity 100% of the resting motor threshold, 50 pulses per train, inter train pause of 10 s, 40 stimulation trains, 2000 pulses/ session)

No Intervention: No repetitive transcranial magnetic stimulation

Outcome Measures

Primary Outcome Measures

  1. Change of craving [Baseline, 1 week later, 1,2,3,4,5,6 months later]

    Craving scores will be assessed with visual analogue scale

  2. Change of protracted-abstinence symptoms [Baseline, 1 week later, 1,2,3,4,5,6 months later]

    Protracted-abstinence symptoms scores will be assessed with protracted symptoms questionnaire

  3. Change of depress symptoms [Baseline, 1 week later, 1,2,3,4,5,6 months later]

    Depress symptoms scores will be assessed with Beck Depression Inventory

  4. Change of anxiety symptoms [Baseline, 1 week later, 1,2,3,4,5,6 months later]

    Anxiety symptoms scores will be assessed with Hamilton Anxiety Scale

  5. Change of impulsive behaviors [Baseline, 1 week later, 1,2,3,4,5,6 months later]

    Impulsive behaviors scores will be assessed with Barratt impulsiveness scale

  6. Change of sleep [Baseline, 1 week later, 1,2,3,4,5,6 months later]

    Sleep scores will be assessed with Pittsburgh sleep quality index

  7. Change of functional connectivity between dorsolateral prefrontal cortex and whole brain [Baseline, 1 week later, 1,3,6 months later]

    Functional connectivity based on dorsolateral prefrontal cortex will be measured with magnetic resonance imaging based on blood oxygen level dependence

  8. Change of gray matter volume of whole brain [Baseline, 1 week later, 1,3,6 months later]

    Gray matter volume will be measured with magnetic resonance imaging (high resolution T1-weighted image)

  9. Change of white matter integrity of whole brain [Baseline, 1 week later, 1,3,6 months later]

    Fractional anisotropy, axial diffusivity and radial diffusivity will be measured with magnetic resonance imaging (diffusion tensor imaging)

  10. Change of availability of dopamine 2 receptor of whole brain [Baseline, 1 month later]

    Accumulation of 11C-raclopride will be analyzed by time-related Positron emission tomography

  11. Change of metabolism of glucose in the brain [Baseline, 1 month later]

    Accumulation of 18F-FDG will be analyzed by time-related Positron emission tomography

Eligibility Criteria

Criteria

Ages Eligible for Study:
25 Years to 55 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria for Heroin-dependent Participants:
  • Clinical diagnosis of heroin addiction

  • Have been receiving treatment in a methadone maintenance treatment program for no less than 6 months

  • have been on a stable dose for at least 1 month before entering the study

  • Right-handed

Inclusion Criteria for Healthy Control Participants:
  • Clinical diagnosis of Healthy Control

  • Right-handed

Exclusion Criteria for all Participants:
  • Current or past psychiatric illness other than heroin and nicotine dependence

  • Neurological signs and/or history of neurological disease

  • History of head trauma

  • History of cardiovascular or endocrine disease

  • Current medical illness or recent medicine use

  • Presence of magnetically active objects in the body

  • Claustrophobia or any other medical condition that would preclude the participant from lying in the PET/MRI scanner for approximately 40 min.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Tangdu Hospital Xi'an Shaanxi China 710038

Sponsors and Collaborators

  • Tang-Du Hospital

Investigators

  • Principal Investigator: Longxiao Wei, phd, Tang-Du Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Tang-Du Hospital
ClinicalTrials.gov Identifier:
NCT04086459
Other Study ID Numbers:
  • Addiction-No.1
First Posted:
Sep 11, 2019
Last Update Posted:
Jan 22, 2021
Last Verified:
Jan 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
Keywords provided by Tang-Du Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 22, 2021