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Interactive Voice Response (IVR) for Methadone Patients

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00237406
First Posted: October 12, 2005
Last Update Posted: March 25, 2010
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Butler Hospital
October 11, 2005
October 12, 2005
March 25, 2010
January 2006
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Complete list of historical versions of study NCT00237406 on ClinicalTrials.gov Archive Site
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Interactive Voice Response (IVR) for Methadone Patients
Interactive Voice Response for Methadone Patients
This study is designed to test whether a telephone call-in program is a feasible way to collect mood and drug-related information in individuals enrolled in a methadone maintenance program.

Participants will complete a baseline interview and a follow-up interview at 5-weeks post-baseline. Two-thirds of the participants will be randomized into the telephone call-in group, and will be asked to complete daily, 10-minute, telephone interviews. To complete these interviews, participants will call into a toll-free telephone interview system with a unique and private Study ID number, and answers questions by using the telephone key pad. Questions during both the face-to-face interviews and the telephone interviews will assess mood, sleep, treatment utilization and drug-related experiences. Participants will be compensated for their time.

Comparison(s): Participants randomized into the telephone component of the study as compared to participants in the interview-only component of the study.

Observational
Observational Model: Cohort
Time Perspective: Prospective
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Probability Sample
Individuals who recently enrolled in methadone maintenance for opioid addiction.
Opioid-Related Disorders
Procedure: interactive voice response
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
50
October 2006
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Inclusion Criteria:

  • Recent enrollment in a methadone maintenance program

Exclusion Criteria:

  • Enrollment in a methadone maintenance program within the prior 3 months
Sexes Eligible for Study: All
18 Years to 75 Years   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT00237406
4065-05
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Butler Hospital
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Principal Investigator: Michael D Stein, MD Rhode Island Hospital
Butler Hospital
March 2010