Text Size

Effect of Patient Participation in Mental Health Care

This study has been completed.
Sponsor:
Collaborators:
Norwegian Foundation for Health and Rehabilitation
The Research Council of Norway
Information provided by (Responsible Party):
Norwegian University of Science and Technology
ClinicalTrials.gov Identifier:
NCT01083225
First received: February 23, 2010
Last updated: January 29, 2013
Last verified: January 2013
History of Changes
  Purpose

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.


Condition Intervention
Mental Health
 Behavioral: Client feedback
Behavioral: Treatment as usual

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Randomised Controlled Trial on the Effect of Individual User Involvement in a Mental Health Center

Resource links provided by NLM:

MedlinePlus related topics: Mental Health
U.S. FDA Resources

Further study details as provided by Norwegian University of Science and Technology:

Primary Outcome Measures:
  • Mental health symptom score (Basis-32) [ Time Frame: Baseline, 6 weeks, 6 months & 12 months ] [ Designated as safety issue: No ]
  • Patient activation (Patient Activation Measure) [ Time Frame: Baseline, 6 weeks, 6 months & 12 months ] [ Designated as safety issue: No ]
  • Alliance (Inpatient treatment alliance scale) [ Time Frame: Baseline, 6 weeks, 6 months & 12 months ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Patient satisfaction (Client Satisfaction Questionnaire) [ Time Frame: Baseline, 6 weeks, 6 months & 12 months ] [ Designated as safety issue: No ]
  • Quality of life (Short form 12) [ Time Frame: Baseline, 6 weeks, 6 months & 12 months ] [ Designated as safety issue: No ]
  • Evaluation of problems (Outcome rating scale) [ Time Frame: Baseline, 6 weeks, 6 months & 12 months ] [ Designated as safety issue: No ]
  • Evaluation of consultations (Session Rating Scale) [ Time Frame: Baseline, 6 weeks, 6 months & 12 months ] [ Designated as safety issue: No ]
  • Evaluation of involvement [ Time Frame: Baseline, 6 weeks, 6 months & 12 months ] [ Designated as safety issue: No ]

Enrollment: 75
Study Start Date: January 2010
Study Completion Date: March 2012
Primary Completion Date: March 2012 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Client feedback Behavioral: Client feedback
Client feedback during consultations using ORS (Outcome rating scale) and SRS (Session rating scale).
Active Comparator: Treatment as usual Behavioral: Treatment as usual
Treatment as usual, consultations

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Over 18 years of age.

Exclusion Criteria:

  • Not able to complete the questionnaires.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01083225

Locations
Norway
St. Olavs Hospital, Nidaros Mental Health Center
Trondheim, Norway
Sponsors and Collaborators
Norwegian University of Science and Technology
Norwegian Foundation for Health and Rehabilitation
The Research Council of Norway
Investigators
Principal Investigator: Aslak Steinsbekk, PhD Norwegian University of Science and Technology
  More Information

No publications provided

Responsible Party: Norwegian University of Science and Technology
ClinicalTrials.gov Identifier: NCT01083225     History of Changes
Other Study ID Numbers: 2008/2/0325
Study First Received: February 23, 2010
Last Updated: January 29, 2013
Health Authority: Norway: Norwegian Social Science Data Services

ClinicalTrials.gov processed this record on May 22, 2013