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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03748875
Other study ID # JDu-006
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date May 1, 2020
Est. completion date December 31, 2022

Study information

Verified date March 2019
Source Shanghai Mental Health Center
Contact Jiang DU, Doctor
Phone 021-64906315
Email dujiangdou@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Amphetamine-type stimulants (ATSs) have become the most important medical issue as well as the social problem. Compared with traditional drugs, ATS are highly neurotoxin and can induce cognitive deficit and psychotic symptoms. Due to lack of efficient medical treatment, psychotherapy and behavioral interventions are the main treatment strategies so far. Mindful-based relapse prevention (MBRP) which combined mindfulness with relapse prevention skills, as a novel intervention, has been widely used in prevent craving and relapse among addictions. While the current research of MBRP mechanism focus on emotion regulation circuit, and there was no study to explore the impulsive circuit, which is the important factor that induce the addiction and relapse. However, there was no report about the influence of MBRP on Prefrontal-striatal circuits. Based on the previous results, the proposed study will focus on evaluating the mechanism of MBRP on prefrontal-striatal circuits, neuropsychological tests and functional MRI will be used to investigate the neurobiological mechanism of MBRP on prefrontal-striatal circuits and related impulsive behaviors.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 200
Est. completion date December 31, 2022
Est. primary completion date January 1, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- 18-45 years old, male or female, with 9 years of education or above, can cooperate with the completion of the questionnaire evaluation;

- Comply with DSM-V diagnostic criteria for amphetamine-based addiction;

- The previous use of amphetamines for not less than 1 year (at least once a week);

- Vision and hearing are normal, or in the normal range after correction. No contraindications for magnetic resonance imaging;

- agree to cooperate with the completion of follow-up evaluation;

- The Mindfulness Attention Awareness Scale score is greater than 50 points.

Exclusion Criteria:

- Severe cognitive dysfunction, such as history of head trauma, cerebrovascular disease, epilepsy, etc., drugs used to promote cognitive function in the last 6 months; intellectual impairment IQ<70;

- There have been other abuse or dependence of psychoactive substances in the past 5 years (excluding nicotine); 100 healthy controls have been publicly collected by the public. Exclude serious physical illness and mental damage. through

- SCID clinical interviews exclude family history of mental disorders and psychosis, no history of substance abuse (except nicotine).

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
mindfulness-based relapse prevention
mindfulness-based relapse prevention, 8 weeks

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Shanghai Mental Health Center

Outcome

Type Measure Description Time frame Safety issue
Primary craving change craving will be measured by visual analogue scale(VAS), participants specify their level of craving by indicating a position along a continuous line between two end-points, score ranges from 0 to 10, 0 refers to the lowest level of craving, 10 refers to the highest level of craving change from baseline, 4,8,12,27and 52 weeks
Primary impulsiveness change impulsiveness will be measured by Barratt Impulsiveness Scale, the scale is a 30 item self-report measure, Rarely/Never = 1,Occasionally = 2,Often = 3,Almost Always/Always = 4. Assessment is indicated by the total score added together. baseline,4,8,12,27and 52 weeks
Primary functional connectivity change between prefrontal cortex and striatum functional connectivity between prefrontal cortex and striatum will be measured by fMRI baseline, 8 and 12weeks
Secondary cognitive function improvement cognitive function improvement will be measured by Cogstate system baseline,4,8,12,27and 52 weeks
Secondary depression level change depression level will be measured by patient health questionnaire-9(PHQ-9). The Patient Health Questionnaire (PHQ) is a multiple-choice self-report inventory, and The PHQ-9 is a tool specific to depression which has 9 items. Assessment is indicated by the total score, which made up by adding together the scores for the scale all seven items.System of scoring is Not at all (0 points),Several days (1 point) More than half the days (2 points) and Nearly every day (3 points).PHQ-9 scores of 5, 10, 15, and 20 represented mild, moderate, moderately severe, and severe depression, respectively. baseline,4,8,12,27and 52 weeks
Secondary anxiety level change anxiety level will be measured by Generalized Anxiety Disorder(GAD-7). it has 7 items and measure severity of various signs of GAD according to reported response categories with assigned points. Assessment is indicated by the total score, which made up by adding together the scores for the scale all seven items.System of scoring is Not at all (0 points),Several days (1 point) More than half the days (2 points) and Nearly every day (3 points). baseline,4,8,12,27and 52 weeks
Secondary addiction severity change addiction severity will be measured by addiction severity index(ASI). ASI is a semi-structured instrument used in face-to-face interviews conducted by clinicians, researchers or trained techniciansIt measures Medical issues relating to drug use, Employment/Support Status, Levels of Alcohol and Drug Use, Legal Issues Arising from Substance Abuse, Family/Social Factors and Psychiatric/Mental Health Status. Severity ratings are based on the following 10 point scale (0-9).0-1: No real problem, treatment not indicated, 2-3: Slight problem, treatment probably not necessary 4-5: Moderate problem, some treatment indicated 6-7: Considerable problem, treatment necessary 8-9: Extreme problem, treatment absolutely necessary baseline,4,8,12,27and 52 weeks
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