- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01796223
Effects of Systematic Patient Feedback on Therapy Outcome
August 31, 2018 updated by: Norwegian University of Science and Technology
Effects of Systematic Patient Feedback on Therapy Outcome and Dropout: A Randomized Controlled Study on Adult Out-patients at a Community Mental Health Centre.
The aim of this study is to evaluate the effects of a feedback-system in psychotherapy on adult out-patients at a community mental health centre.
It is hypothesized that the intervention will lead to more effective treatment, decreasing treatment dropout as well as improving patient-therapist relationship and patient activation in treatment.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
170
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Trondheim, Norway
- Tiller Distriktspsykiatriske Senter
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
The aim is to include a total of 128 patients.
Inclusion Criteria:
- Referred for treatment of mental disorder(s)
Exclusion Criteria:
- Psychiatric emergency
- Poor/no understanding of Norwegian language
- Lack of ability to execute the practical procedures required for the project
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Feedback
Feedback system included in psychotherapy
|
The Partners for Change Outcome Management System, administered at the beginning and ending of every therapy session.
Other Names:
|
|
Active Comparator: control
Psychotherapy as usual
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Health care utilization
Time Frame: 12 months
|
Referral- and drop-out rate
|
12 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Symptom level
Time Frame: T 0 (baseline) and T4 (6 months, end of treatment)
|
Outcome Rating Scale and BASIS 32 and WHO-5
|
T 0 (baseline) and T4 (6 months, end of treatment)
|
|
Patient satisfaction
Time Frame: T0, T2 (2 months), T4 (6 months, end of treatment)
|
Client Satisfaction Questionnaire (CSQ-8; Attkinson & Zwick, 1982)
|
T0, T2 (2 months), T4 (6 months, end of treatment)
|
|
Level of functioning
Time Frame: T1 (1 hour start of treatment) and T4 (6 months or end of treatment)
|
Global Assessment of Functioning (GAF; Hall, 1995)
|
T1 (1 hour start of treatment) and T4 (6 months or end of treatment)
|
|
Preferences for involvement in decision making
Time Frame: T0, T2 (2 months) and T3 (3 months)
|
Modified Control Preferences Scale (6 items)
|
T0, T2 (2 months) and T3 (3 months)
|
|
Patient Activation Measure
Time Frame: T0, T1 (1 hour start of treatment), T3 (3 months) and T4 (6 months)
|
Patient Activation Measure Mental Health Questionnaire (13 items)
|
T0, T1 (1 hour start of treatment), T3 (3 months) and T4 (6 months)
|
|
Alliance
Time Frame: T1 (1 hour start of treatment), T2 (2 months
|
Working Alliance Inventory (WAI-S)
|
T1 (1 hour start of treatment), T2 (2 months
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Use of health services
Time Frame: 12 months
|
Number of visits at general practitioner or other health services
|
12 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Chair: Olav M Linaker, MD, PhD, Norwegian University of Science and Technology
- Principal Investigator: Mariela M Lara, MA, National Taiwan Normal University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Brattland H, Koksvik JM, Burkeland O, Grawe RW, Klockner C, Linaker OM, Ryum T, Wampold B, Lara-Cabrera ML, Iversen VC. The effects of routine outcome monitoring (ROM) on therapy outcomes in the course of an implementation process: A randomized clinical trial. J Couns Psychol. 2018 Oct;65(5):641-652. doi: 10.1037/cou0000286. Epub 2018 Aug 16.
- Brattland H, Koksvik JM, Burkeland O, Klockner CA, Lara-Cabrera ML, Miller SD, Wampold B, Ryum T, Iversen VC. Does the working alliance mediate the effect of routine outcome monitoring (ROM) and alliance feedback on psychotherapy outcomes? A secondary analysis from a randomized clinical trial. J Couns Psychol. 2019 Mar;66(2):234-246. doi: 10.1037/cou0000320. Epub 2019 Jan 31.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 1, 2012
Primary Completion (Actual)
June 1, 2017
Study Completion (Actual)
June 1, 2017
Study Registration Dates
First Submitted
February 19, 2013
First Submitted That Met QC Criteria
February 19, 2013
First Posted (Estimate)
February 21, 2013
Study Record Updates
Last Update Posted (Actual)
September 5, 2018
Last Update Submitted That Met QC Criteria
August 31, 2018
Last Verified
August 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2011/1271 (Registry Identifier: Regional committee for medical research ethics)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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