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Comparison of the effectiveness of the clinical guide for the treatment of sexual addiction disorder in individuals with and without a history of stimulant use

Developing a clinical guideline for treatment of sex addiction and comparing its efficacy in individuals with and without a history of stimulant use.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200905048628N1
Enrollment
60
Registered
2021-01-01
Start date
2020-11-30
Completion date
Unknown
Last updated
2021-02-22

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

Conditions

sexual addiction disorder, stimulant use disorder. Other sexual dysfunction not due to a substance or known physiological condition

Interventions

Intervention 1: Intervention group1: People with sexual addiction disorder
According to the handbook for guideline development (World Health Organization, 2012) and based on literature review, the clinical guide for the treatment of sexual addiction disorder in the form of 1
For the control group, the placebo will be presented in the form of books and educational videos in the field of treatment of sexual addiction disorder. Intervention 4: Control group 2: People with se
For the control group, the placebo will be presented in the form of books and educational videos in the field of treatment of sexual addiction disorder.

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: receiving a diagnosis of stimulant use disorder receiving a diagnosis of sexual addiction disorder

Exclusion criteria

Exclusion criteria: Existence of mental retardation Symptoms of psychosis Bipolar disorder Acute thoughts of suicide Opioid use Drug use Having any organic disorders such as a history of head trauma with anesthesia, seizures, brain tumors, etc., which has led to cognitive and psychological disorders.

Design outcomes

Primary

MeasureTime frame
People who have a score of 53 or higher in the Hypersexual Behavior Inventory. Timepoint: Measuring the score of the Hypersexual Behavior Inventory before the intervention (pre-test), after the intervention (post-test) and 2-month follow-up. Method of measurement: Hypersexual Behavior Inventory.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactArash Javaheri

Iran University of Medical Sciences

ajavaheri68@gmail.com+98 31 3225 5571

Outcome results

None listed

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