Amphetamine Addiction Clinical Trial
Official title:
The Application of Cognitive Rehabilitation Therapy for Amphetamine-type Stimulants Addiction
NCT number | NCT03318081 |
Other study ID # | MZhao-008 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | October 20, 2017 |
Est. completion date | May 1, 2018 |
Verified date | January 2020 |
Source | Shanghai Mental Health Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The computerized cognitive rehabilitation therapy will be used to treat amphetamine-type stimulant (ATS) addiction.
Status | Completed |
Enrollment | 40 |
Est. completion date | May 1, 2018 |
Est. primary completion date | December 31, 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility |
Inclusion Criteria: 1. diagnosed MA dependence in accordance with the fourth edition of the American Psychiatric Association's Diagnostic and Statistical Manual of Mental Disorders (DSM-IV) (Association, 2000); 2. more than 9 years of education; 3. aged of 18-60 years old; 4. normal vision, audition and no color blindness; 5. receive no detoxification medications during treatment and 6. right handedness. Exclusion Criteria: 1. current medical diseases that required hospitalization or regular monitoring; 2. serious physical or neurological illness that required pharmacological treatment affecting cognitive function; 3. history of major psychiatric disorder such as bipolar disorder, schizophrenia, depression and disorders of high comorbidity with substance abuse/dependence; 4. neurological diseases such as stroke, seizure, migraine, head trauma 5. substance dependence other than nicotine, within the past 5 years; 6. intelligence quotient (IQ) <70. |
Country | Name | City | State |
---|---|---|---|
China | Shanghai Compulsory Isolation Detoxification Center | Shanghai |
Lead Sponsor | Collaborator |
---|---|
Shanghai Mental Health Center |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change from Baseline Craving for ATS assessed by Visual Analog Scales (VAS) at 1 month , 3 month and 6 months | evaluate all participants' craving for ATS by Visual Analog Scales (VAS): The scores of the VAS were 0-10 points. 10 points reflect the highest level of individual's craving, and 0 point reflect no craving in patient. | Baseline, 1 month, 3 month and 6 months | |
Secondary | Cognitive function assessed by CogState Battery (CSB) | evaluate all participants' cognitive function by the computerized CogState Battery (CSB) Chinese version: The five tasks listed below were examined. International shopping list task (ISLT, verbal learning and memory), the score is defined as the total number of correct responses. Continuous paired association learning task (CPAL) taps spatial working memory. Groton maze learning task (GML) taps problem solving/error monitoring. The scores of CPAL and GML tasks are the total number of errors. Social emotional cognition task (SEC, social cognition) asks the subjects to pick out the different facial expressions. Two back task (TWOB, working memory) requires subjects to decide whether a card is identical to the one shown just before. The scores of TWOB and SEC tasks are the proportion of correct responses, denoting the accuracy of performance. The higher values represent a better outcome in ISL, SEC and TWOB. The higher values represent a worse outcome in GML and CPAL. | Baseline, 1 month, 3 month and 6 months | |
Secondary | Changing of response inhibition ablility assessed by Balloon Analogue Risk Task (BART) | evaluate all participants' response inhibition function by Balloon Analogue Risk Task (BART): Several indices were computed to represent the behavioral performance, including the ratio of all pumps to numbers of win trials, the ratio of pumps to numbers in win trials, and the number of win trials. The higher values represent a worse outcome. | Baseline, 1 month, 3 month and 6 months | |
Secondary | Number of participants who relapse | Follow up with patients after discharge, evaluate number of participants who relapse. The higher values represent a worse outcome. | 1 month, 3 month and 6 months |
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