Evaluation of Case Management to Improve the Outpatient Care of Alcohol-related Disorders

Sponsor
University Hospital Freiburg (Other)
Overall Status
Completed
CT.gov ID
NCT00314067
Collaborator
(none)
112
2
3
13
56
4.3

Study Details

Study Description

Brief Summary

The purpose of this study is to disseminate and transfer the comprehensive quality management interventions (CQM) for alcohol-related disorders in primary care developed during the first funding phase into routine care. The two steps are (1) to optimize the CQM approach and (2) to investigate the dissemination and transfer into routine care in a randomized controlled trial.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Online Comprehensive Quality Management System (CQM) of alcohol-related disorders in primary care
  • Procedure: Physician training
  • Procedure: Practice team training
N/A

Detailed Description

In the first funding phase the project AQAH ("Ambulantes Qualitätsmanagement alkoholbezogener Störungen in der hausärztlichen Praxis"-"comprehensive quality management for alcohol-related disorders in primary care") systematically investigated three issues: (1) the outpatient care system and evidence-base for screening, diagnosis and treatment was examined; it developed (2) a comprehensive quality management system (CQM) consisting of documentation material, a pathway of care and evidence-based practice guidelines; (3) the effects of the CQM on the detection and treatment of alcohol-related disorders were investigated in a randomized controlled pre-post design and the results show positive effects of the CQM. In the second funding phase (a 3 year bi-center project) the purpose is now to disseminate and transfer the CQM into routine care. The two steps are (1) to optimize the CQM approach and (2) to investigate the dissemination and transfer into routine care in a randomized trial. (1) The paper-based AQAH-practice guidelines are transformed into an interactive electronic version with online patient documentation and evaluation, decision support measures as well as links to specialists and an e-learning tool. (2) After pilot testing in the AQAH-study-networks, an active transfer to the greater regions of Südbaden and Südwürttemberg will be performed in a parallel group cluster randomized controlled trial with GP practices as unit of randomization. Outcome data will be collected concerning the acceptance of the system and the quality of care delivered.

Comparison(s): (1) Use of the interactive electronic version of the CQM for alcohol-related disorders with a special training for general practitioners, compared to (2) use of the CQM with additional education for the whole practice team and organizational re-structuring advice, compared to (3) a control group who uses the CMQ without any special training.

Study Design

Study Type:
Interventional
Actual Enrollment :
112 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Official Title:
Comprehensive Quality Management in Out-patient Care for Alcohol-related Disorders (AQAH). Transfer and Dissemination Into Routine Practice
Study Start Date :
Jul 1, 2006
Actual Primary Completion Date :
May 1, 2007
Actual Study Completion Date :
Aug 1, 2007

Arms and Interventions

Arm Intervention/Treatment
Experimental: 1

Procedure: Online Comprehensive Quality Management System (CQM) of alcohol-related disorders in primary care

Procedure: Physician training

Experimental: 2

Procedure: Online Comprehensive Quality Management System (CQM) of alcohol-related disorders in primary care

Procedure: Physician training

Procedure: Practice team training

Active Comparator: 3

Procedure: Online Comprehensive Quality Management System (CQM) of alcohol-related disorders in primary care

Outcome Measures

Primary Outcome Measures

  1. Acceptance of the CQM-system: Number of actively participating practices []

  2. Adherence to the system: relative numbers of screened, documented and followed-up patients []

Secondary Outcome Measures

  1. Quality of care provided: Patients that are adequately treated and followed-up []

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • General practitioner

  • Possibility to use broad-band internet

Exclusion Criteria:
  • none

Contacts and Locations

Locations

Site City State Country Postal Code
1 Freiburg University Hospital, Dept. of Psychiatry and Psychotherapy Freiburg Germany 79104
2 University Hospital for Psychiatry and Psychotherapy, Tübingen Tübingen Germany 72076

Sponsors and Collaborators

  • University Hospital Freiburg

Investigators

  • Principal Investigator: Martin Härter, Prof. Dr. Dr., Freiburg University Hospital, Dept. of Psychiatry and Psychotherapy
  • Principal Investigator: Michael Berner, Dr., Freiburg University Hospital, Dept. of Psychiatry and Psychotherapy
  • Study Chair: Daniela Ruf, Dipl. Psych., Freiburg University Hospital, Dept. of Psychiatry and Psychotherapy
  • Study Chair: Götz Mundle, PD Dr., Oberbergklinik, Hornberg and University Hospital for Psychiatry and Psychotherapy, Tübingen
  • Study Chair: Monika Lohmann, Dipl. Psych., University Hospital for Psychiatry and Psychotherapy, Tübingen

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00314067
Other Study ID Numbers:
  • BMBF-01EB0412
First Posted:
Apr 12, 2006
Last Update Posted:
Oct 18, 2013
Last Verified:
Jun 1, 2008

Study Results

No Results Posted as of Oct 18, 2013