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Effect of neurofeedback and cognitive rehabilitation in treatment of opium and heroin addicts

Comparison of the Effectiveness of LORETA Z Score Neurofeedback with Cognitive Rehabilitation on Decreasing of Craving in Opioid Addicts

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170924036386N1
Enrollment
40
Registered
2018-01-08
Start date
2017-07-23
Completion date
Unknown
Last updated
2018-05-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Opioids Addiction. Mental and behavioural disorders due to use of opioids

Interventions

Intervention 1: Cognitive rehabilitation by Dot Probe software. 15 sessions(each session: 20 minute) for everybody in cognitive rehabilitation group will be done in MMT center. Pre and post tests of

Sponsors

Zanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Opium and heroin addicts Age range: 18-70 Males Drug use: Methadone

Exclusion criteria

Exclusion criteria: Age> 70 y/o Females Methadone> 100 mg/d Non opioides addicts

Design outcomes

Primary

MeasureTime frame
Craving. Timepoint: Begin-mid- end of study. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
??Addiction Severity Index. Timepoint: At the beginning and end of the study. Method of measurement: Questionnaire.;Recovery assessment scale. Timepoint: At the beginning and end of the study. Method of measurement: Questionnaire.;LDQ. Timepoint: At the beginning and end of the study. Method of measurement: Questionnaire.;Stroop Task. Timepoint: At the beginning and end of the study. Method of measurement: Questionnaire.;Quality of Life. Timepoint: At the beginning and end of the study. Method of measurement: Questionnaire.;Anxiety. Timepoint: At the beginning, middle and end of the study. Method of measurement: Questionnaire.;Depression. Timepoint: At the beginning, middle and end of the study. Method of measurement: Questionnaire.;Response inhibition. Timepoint: At the beginning and end of the study. Method of measurement: Questionnaire.;Attention bias. Timepoint: At the beginning and end of the study. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAlireza Faridi

Zanjan University of Medical Sciences

arf1347@yahoo.com+98 24334206519

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026