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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: August 18, 2015
Last verified: August 2015
  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
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:


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 ]
  • Patient activation (Patient Activation Measure) [ Time Frame: Baseline, 6 weeks, 6 months & 12 months ]
  • Alliance (Inpatient treatment alliance scale) [ Time Frame: Baseline, 6 weeks, 6 months & 12 months ]

Secondary Outcome Measures:
  • Patient satisfaction (Client Satisfaction Questionnaire) [ Time Frame: Baseline, 6 weeks, 6 months & 12 months ]
  • Quality of life (Short form 12) [ Time Frame: Baseline, 6 weeks, 6 months & 12 months ]
  • Evaluation of problems (Outcome rating scale) [ Time Frame: Baseline, 6 weeks, 6 months & 12 months ]
  • Evaluation of consultations (Session Rating Scale) [ Time Frame: Baseline, 6 weeks, 6 months & 12 months ]
  • Evaluation of involvement [ Time Frame: Baseline, 6 weeks, 6 months & 12 months ]

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   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Over 18 years of age.

Exclusion Criteria:

  • Not able to complete the questionnaires.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

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

Publications:
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: August 18, 2015

ClinicalTrials.gov processed this record on February 20, 2017