Interactive Voice Response (IVR) for Methadone Patients

Opioid-Related Disorders Clinical Trial

Official title:

Interactive Voice Response for Methadone Patients

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00237406
• Other study ID #: 4065-05
• Status: Completed
• Phase: Phase 3
• First received: October 11, 2005
• Last updated: March 24, 2010
• Start date: January 2006
• Est. completion date: October 2006

Study information

• Verified date: March 2010
• Source: Butler Hospital
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Observational

Clinical Trial Summary

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.

Description:

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 50
• Est. completion date: October 2006
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Recent enrollment in a methadone maintenance program

Exclusion Criteria:

• Enrollment in a methadone maintenance program within the prior 3 months

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

• Opioid-Related Disorders

Intervention

Procedure:
• interactive voice response

Locations

Country	Name	City	State
United States	Rhode Island Hospital	Providence	Rhode Island

Sponsors (1)

Lead Sponsor	Collaborator
Butler Hospital

Country where clinical trial is conducted

United States,