Transcranial Magnetic Stimulation for Treatment of Methamphetamine Dependence

Sponsor
Shanghai Mental Health Center (Other)
Overall Status
Completed
CT.gov ID
NCT03827785
Collaborator
Wuxi Mental Health Center, Jiangsu Provence, China (Other), Suzhou Guangji Hospital, Jiangsu Provence, China (Other), Wuhan Mental Health Center, Hubei Provence, China (Other), Yunnan Institute For Drug Abuse (Other)
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Study Details

Study Description

Brief Summary

Repetitive transcranial magnetic stimulation (rTMS) was used to treat methamphetamine (MA) addiction in previous studies, while the evidence-based protocols still required. The aim of this research is to evaluating the effectiveness and safety of rTMS treatment in improving the days of abstinence maintenance. In addition, treatment effect on cognitive impairment, psychological craving and depression are also evaluated during the study.

Condition or Disease Intervention/Treatment Phase
  • Device: rTMS treatment group
  • Device: sham rTMS treatment group
N/A

Detailed Description

First, a multicenter, double-blind, randomized control study is going to be carried out. 100 recruited patients will be randomized assigned to the intervention group and the control group, receiving either 4-week of repetitive transcranial magnetic stimulation (rTMS) treatment or 4-week of sham rTMS treatment. Both groups will receive 12-week urine drug test follow-up (1 time per week). Negative rate of urine test during the follow-up period is set as primary outcome. Cognitive function, craving, depression are also evaluated before and after the intervention.

Secondly, another 40 patients will be recruited from these 100 patients (20 subjects each group). Magnetic resonance spectroscopy (MRS) test is applied to investigate the potential neurobiological mechanism of rTMS treatment. This study will be very helpful to develop an evidence-based rTMS treatment protocols for MA dependent patients and decrease risk of relapse for both the patients and their families.

Study Design

Study Type:
Interventional
Actual Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Care Provider, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
The Efficacy and Safety of Repeated Transcranial Magnetic Stimulation for Treatment of Methamphetamine Dependence: a Multicenter, Double-blind, Randomized Controlled Clinical Trial
Actual Study Start Date :
Feb 1, 2019
Actual Primary Completion Date :
Sep 1, 2020
Actual Study Completion Date :
Dec 12, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: rTMS treatment group

Stimulate the dorsal lateral prefrontal cortex with the iTBS pattern. The therapy will be conducted for 30 days.

Device: rTMS treatment group
For rTMS treatment, we will stimulate the dorsal lateral prefrontal cortex of each patients using the iTBS pattern everyday. Treatment will lasted for 30 days.

Sham Comparator: sham rTMS treatment group

Stimulate the dorsal lateral prefrontal cortex with the sham iTBS pattern and coil. The therapy will be conductedfor 30 days.

Device: sham rTMS treatment group
For sham rTMS treatment, we will stimulate the dorsal lateral prefrontal cortex of each patients using the sham iTBS pattern and sham coil everyday for 30 minutes. Treatment will lasted for 30 days.

Outcome Measures

Primary Outcome Measures

  1. Negative rate urine test [12 weeks]

    After treatment, patients will be asked to participate urine test for 12 times once a week. Loss of visit or rejection for urine test will be treated as urine test positive. Negative rate of urine drug test = actual number of negative urine tests / 12.

Secondary Outcome Measures

  1. Change of Craving assessed by Visual Analog Scale [12 weeks]

    evaluate all participants' craving for for methamphetamine assessed by Visual Analog Scales (VAS). Score of VAS range from 0 to 10, and higher values represent high level of craving.

  2. Cognitive function assessed by CogState Battery (CSB) [12 weeks]

    evaluate all participants' cognitive function by the computerized CogState Battery (CSB) Chinese version

  3. Depression status assessed by Hamilton depression scale (HAMD-17) [12 weeks]

    Evaluate all participants' depression status by Hamilton depression scale (HAMD-17) HAMD can be summarized into 7 types of factor structure: (1) anxiety/somatization:; (2) weight: weight loss (3) Cognitive obstacles; (4) day and night changes; (5) Block; (6) sleep disorder; (7) feeling of despair. The total score can reflect the severity of the symptom, that is, The lighter the symptoms, the lower the score, and vice versa. Mild depression: HAMD 17 scores > 7 points, ≤ 17 points; moderate depression: HAMD 17 scores > 17 points, ≤ 24 points; severe depression: HAMD 17 scores > 24 points.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 45 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. In accordance with the Diagnostic and Statistical Manual of Mental Disorders-5 (DSM-5) for methamphetamine (MA) use disorders

  2. Junior high school degree or above

  3. Normal vision and hearing

  4. Dextromanual

  5. Less than one month before last drug use

Exclusion Criteria:
  1. Have a disease that affect cognitive function such as history of head injury, cerebrovascular disease, epilepsy, etc

  2. Have cognitive-promoting drugs in the last 6 months

  3. Other substance abuse or dependence in recent five years (except nicotine)

  4. Mental impairment, Intelligence Quotient (IQ) < 70

  5. Mental disorders

  6. Physical disease

Contacts and Locations

Locations

Site City State Country Postal Code
1 Shanghai Rehabilitation Center Shanghai China 200010

Sponsors and Collaborators

  • Shanghai Mental Health Center
  • Wuxi Mental Health Center, Jiangsu Provence, China
  • Suzhou Guangji Hospital, Jiangsu Provence, China
  • Wuhan Mental Health Center, Hubei Provence, China
  • Yunnan Institute For Drug Abuse

Investigators

  • Principal Investigator: Haifeng Jiang, Shanghai Mental Health Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Shanghai Mental Health Center
ClinicalTrials.gov Identifier:
NCT03827785
Other Study ID Numbers:
  • HFJiang-002
First Posted:
Feb 1, 2019
Last Update Posted:
Sep 16, 2021
Last Verified:
Sep 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Shanghai Mental Health Center

Study Results

No Results Posted as of Sep 16, 2021