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Improving Substance Abuse Counseling Adherence Using Web-based Videoconferencing

Improving Substance Abuse Counseling Adherence Using Web-based Videoconferencing

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01142609
Enrollment
85
Registered
2010-06-11
Start date
2009-12-31
Completion date
2012-08-31
Last updated
2013-04-04

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

Conditions

Substance Abuse Disorder

Keywords

Web based videoconferencing, methadone, substance abuse counseling

Brief summary

This research is being done to compare the effectiveness of standard on-site, in-person counseling with Internet web-based videoconferencing (e-therapy) in drug-dependent patients in opioid-agonist treatment programs. The study is looking to see if there are any differences in satisfaction or in treatment outcome if counseling sessions are given by e-therapy compared to standard, in-person counseling given in the clinic. The e-therapy happens in real time- it works very much like standard therapy in the clinic except that the patient is in his or her own home (or other convenient location outside the clinic) and talks to and sees the therapist through an Internet connection on the computer (the therapist will usually be at the clinic).

Detailed description

This study will be the first to evaluate the efficacy of an accredited and currently available, Internet web-based videoconferencing platform to deliver routine schedules of counseling in an opioid agonist treatment program. It has outstanding potential to help determine transportability of this technology to other treatment programs by demonstrating the benefits of integration of web-based therapy with on-site services to expand the continuum of care.

Interventions

BEHAVIORALeGet

eGet individual counseling sessions from home will be scheduled weekly for 12 weeks.

Sponsors

National Institute on Drug Abuse (NIDA)
CollaboratorNIH
Johns Hopkins University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

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

Inclusion criteria

* Access to a computer with Internet capability * Full adherence to their routine counseling schedule over the previous 30-days * Negative urine specimens over the previous 30-days * Patient at ATS for 90 days

Exclusion criteria

* No access to a computer with Internet capability

Design outcomes

Primary

MeasureTime frameDescription
Counseling efficacyWeekly for 12 weeksAttendance to individual counseling sessions, both online and on-site will be tracked weekly for the duration of the study.
Reinforcement value (eGetgoing)Monthly for 3 monthsSubjects will complete monthly surveys to evaluate the reinforcement value of eGetgoing using a multiple choice design that will compare its perceived value to other aspects of routine treatment (e.g., take-home medications).
Reinforcement value (on-site)BaselineSubjects will complete a survey to evaluate the reinforcement value of eGetgoing using a multiple choice design that will compare its perceived value to other aspects of routine treatment (e.g., take-home medications).

Secondary

MeasureTime frameDescription
Program SatisfactionBaseline and monthly for 3 monthsSubjects will complete a survey to assess their overall program satisfaction
Treatment costBaseline and Month 3Subjects will complete surveys to measure treatment related time and monetary travel costs.
Therapeutic relationshipBaseline and monthly for 3 monthsSubjects and their therapists will complete surveys to assess qualities of the therapeutic relationship.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026