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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01083225
Other study ID # 2008/2/0325
Secondary ID
Status Completed
Phase N/A
First received February 23, 2010
Last updated August 18, 2015
Start date January 2010
Est. completion date March 2012

Study information

Verified date August 2015
Source Norwegian University of Science and Technology
Contact n/a
Is FDA regulated No
Health authority Norway: Norwegian Social Science Data Services
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the effect of individual user involvement in an outpatient mental health center. The intervention consists of patients completing a self-report symptom and problem questionnaire and reviewing it with a clinician.


Recruitment information / eligibility

Status Completed
Enrollment 75
Est. completion date March 2012
Est. primary completion date March 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Over 18 years of age.

Exclusion Criteria:

- Not able to complete the questionnaires.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Client feedback
Client feedback during consultations using ORS (Outcome rating scale) and SRS (Session rating scale).
Treatment as usual
Treatment as usual, consultations

Locations

Country Name City State
Norway St. Olavs Hospital, Nidaros Mental Health Center Trondheim

Sponsors (3)

Lead Sponsor Collaborator
Norwegian University of Science and Technology Norwegian Foundation for Health and Rehabilitation, The Research Council of Norway

Country where clinical trial is conducted

Norway, 

References & Publications (1)

Rise MB, Eriksen L, Grimstad H, Steinsbekk A. The long-term effect on mental health symptoms and patient activation of using patient feedback scales in mental health out-patient treatment. A randomised controlled trial. Patient Educ Couns. 2016 Jan;99(1): — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Mental health symptom score (Basis-32) Baseline, 6 weeks, 6 months & 12 months No
Primary Patient activation (Patient Activation Measure) Baseline, 6 weeks, 6 months & 12 months No
Primary Alliance (Inpatient treatment alliance scale) Baseline, 6 weeks, 6 months & 12 months No
Secondary Patient satisfaction (Client Satisfaction Questionnaire) Baseline, 6 weeks, 6 months & 12 months No
Secondary Quality of life (Short form 12) Baseline, 6 weeks, 6 months & 12 months No
Secondary Evaluation of problems (Outcome rating scale) Baseline, 6 weeks, 6 months & 12 months No
Secondary Evaluation of consultations (Session Rating Scale) Baseline, 6 weeks, 6 months & 12 months No
Secondary Evaluation of involvement Baseline, 6 weeks, 6 months & 12 months No
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