Skip to content

Efficacy of Escitalopram in the Treatment of Internet Addiction

Efficacy of Escitalopram in the Treatment of Internet Addiction

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00565422
Enrollment
31
Registered
2007-11-30
Start date
2002-12-31
Completion date
2004-10-31
Last updated
2008-05-28

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

Conditions

Internet Addiction

Keywords

Internet addiction, Problematic internet use, Escitalopram, Lexapro

Brief summary

The purpose of this study was to determine whether Lexapro (Escitalopram) is safe and effective in treating problematic internet use.

Detailed description

Many individuals experience marked distress and functional impairments as a result of their perceived inability to control their 'non-essential' (non-job/school related) use of the Internet. Frequently these people develop a preoccupation with the Internet, a need for escape to the Internet, and increasing irritability when trying to cut back use of the Internet. There have been no studies to date looking at the effectiveness of medications in the treatment of this disorder. In our clinical experience, we find these patients with Internet addiction usually respond to serotonin reuptake inhibitors within 12 weeks. This study will examine the efficacy of escitalopram in Internet addiction among adults.

Interventions

DRUGEscitalopram

10 mg/day

Sponsors

Forest Laboratories
CollaboratorINDUSTRY
Icahn School of Medicine at Mount Sinai
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. Subject has signed an informed consent form 2. Current diagnosis of Internet addiction 3. Age ³ 18 4. Subject must be able to take oral medication 5. Subject may be in psychotherapy initiated at least three months prior to Screening. Subject must not discontinue or otherwise alter this therapy during the study. 6. In the opinion of the investigator, the subject is capable of complying with all study procedures.

Exclusion criteria

1. Current suicidal or homicidal ideation 2. Subject has a primary diagnosis of schizophrenia or other psychotic disorders 3. Subject has a primary diagnosis of Bipolar I disorder 4. Current pedophilia 5. Current DSM-IV diagnosis of substance dependence or abuse, excluding nicotine 6. Women of child-bearing potential who are pregnant, nursing, or not using contraception 7. Use of antidepressants at a therapeutic level for the treatment of problematic internet use within 2 weeks prior to study entry (or 4 weeks for use of MAOIs, or 6 weeks for use of fluoxetine) 8. Current use of antidepressants at a therapeutic level for the treatment of a disorder other than problematic internet use 9. Subject has any organic mental disorder 10. Clinically significant unstable medical disorder

Design outcomes

Primary

MeasureTime frame
length of non-essential Internet use in hours/week as well as CGI-Improvementbaseline and biweekly for 10 weeks

Secondary

MeasureTime frame
ratings on depression, anxiety, impulsivity, self-esteem, obsessive-compulsive symptomsbaseline and biweekly for 10 weeks

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 5, 2026