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Clinical Trials/NCT00798044
NCT00798044
Completed
Not Applicable

Patient Feedback Effectiveness Study

University of Pennsylvania2 sites in 1 country118 target enrollmentNovember 2006

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Substance Use Disorders
Sponsor
University of Pennsylvania
Enrollment
118
Locations
2
Primary Endpoint
clinician average weekly caseload patient-rated therapeutic alliance
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

The purpose of the study is to determine if a semi-automated quality improvement system that provides addiction counselors with feedback on their average treatment satisfaction and therapeutic alliance (as rated by patients currently in treatment) is superior to no feedback in 32 community-based outpatient addiction treatment clinics.

Detailed Description

Quality improvement (Ql) methods are a cornerstone of business and healthcare management throughout the United States yet there have been few studies of Ql interventions in addiction treatment settings. The proposed study tests the effectiveness of one Ql system - Patient Feedback (PF) - at increasing outpatient group therapy attendance and self-reported abstinence. The feasibility and acceptability of PF was established in a six-site study conducted within the National Drug Abuse Treatment Clinical Trials Network. In the proposed study, 32 community-based outpatient treatment programs with approximately 250 clinicians will be randomly assigned to PF, or usual clinic practices. In the PF condition, every week fro 12 weeks clinic patients are invited to complete a 12-item, self-administered survey in which they rate therapeutic alliance and treatment satisfaction, and report past week substance use. These anonymous surveys are faxed by clinic staff to a University of Pennsylvania data center where a custom software application converts the surveys into feedback reports and posts them to a password protected website. Clinicians can access their caseload feedback reports and aggregated reports for the whole clinic; supervisors can only access the aggregated clinic reports. On a monthly basis staff meet as a team to review the feedback reports and develop Ql plans intended to yield improvements in select Ql indicators. The PF website and the monthly PF e-newsletter provide social recognition, clinical resources, and a virtual community for participating clinicians. After 12 weeks, participants in both conditions complete follow-up measures and then both groups are given open access to PF for 12 additional months. During "sustainability phase" staff usage of the PF website is monitored. Alternate versions of the PF Survey are introduced during the sustainability study, including one that monitors HIV risk behavior. The rapid processing of surveys enables near real time feedback to clinic staff. Organizations may share their feedback reports with funding sources, regulatory agencies, policy makers, and other stakeholders. This centralized, semi-automated feedback system eases fulfillment of accreditation requirements and as such, reduces the cost of clinic operations.

Registry
clinicaltrials.gov
Start Date
November 2006
End Date
April 2009
Last Updated
14 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Paul Crits-Christoph

Professor of Psychology in Psychiatry

University of Pennsylvania

Eligibility Criteria

Inclusion Criteria

  • program: adult, outpatient, non-methadone maintenance substance abuse treatment programs
  • clinician: must be leading at least one weekly group with minimum of 5 patients
  • must be working at least 20% time at facility

Exclusion Criteria

  • clinics with fewer than 5 clinicians who conduct weekly group counseling
  • clinics in which fewer than 50% of clinicians agree to participate

Outcomes

Primary Outcomes

clinician average weekly caseload patient-rated therapeutic alliance

Time Frame: 12 weeks

Study Sites (2)

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