Skip to main content
Clinical Trials/NCT01142609
NCT01142609CompletedNot Applicable

Improving Substance Abuse Counseling Adherence Using Web-based Videoconferencing

Johns Hopkins University2 sites in 1 country85 target enrollmentStarted: December 2009Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
85
Locations
2
Primary Endpoint
Counseling efficacy

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
None

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts 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

Outcomes

Primary Outcomes

Counseling efficacy

Time Frame: Weekly for 12 weeks

Attendance to individual counseling sessions, both online and on-site will be tracked weekly for the duration of the study.

Reinforcement value (eGetgoing)

Time Frame: Monthly for 3 months

Subjects 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)

Time Frame: Baseline

Subjects 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 Outcomes

  • Program Satisfaction(Baseline and monthly for 3 months)
  • Treatment cost(Baseline and Month 3)
  • Therapeutic relationship(Baseline and monthly for 3 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Van King

Associate Professor

Johns Hopkins University

Study Sites (2)

Loading locations...

Similar Trials