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Clinical Trials/NCT00623922
NCT00623922
Completed
Not Applicable

The Effect of Patient Education on Coping and Well Being in Patients With Arthritis.

Norwegian University of Science and Technology1 site in 1 country141 target enrollmentFebruary 2008
ConditionsPolyarthritis

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Polyarthritis
Sponsor
Norwegian University of Science and Technology
Enrollment
141
Locations
1
Primary Endpoint
Self efficacy
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The purpose of this study is to explore the effect of patient education (PE) in patients with arthritis. PE has become a task that is dictated by law in Norway, and is increasingly used as an element in the treatment of patients with chronic complaints. Our hypothesis is that

  • PE delivered as group education, followed by an individual nurse consultation increases the patients wellbeing an ability to cope with the disease.

Detailed Description

There has been a rather long tradition of PE for patients with arthritis. A recent systematic review found that PE had small short-term effects on disability, joint counts, patient global assessment, psychological status and depression, but this effect disappeared on the latest time of follow up (3-14 months). A recent large British study also failed to show an effect on pain, physical functioning, or contact with primary care after 12 months, but found a significant effect on anxiety and improved the participants' perceived self efficacy. This indicates that the present forms of interventions fails to show a long term effect. One possible reason for the lack of long term effect might be that these interventions are given to groups only. Patients seem to prefer one-to-one interaction regarding information about the disease and its treatment together with emotional aspects, while education in groups are preferred for physical training and relational topics.

Registry
clinicaltrials.gov
Start Date
February 2008
End Date
March 2010
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Polyarthritis
  • 18-80 years
  • native Norwegian speaking
  • able to understand and participate in the PE program

Exclusion Criteria

  • Participated in a patient educational program the latest 12 months

Outcomes

Primary Outcomes

Self efficacy

Time Frame: Baseline, 4 and 12 months

Well being (Arizona Integrative Outcomes Scale)

Time Frame: Baseline, 4 and 12 months

Secondary Outcomes

  • Educational Needs Assessment Tools(Baseline, 4 and 12 months)
  • Patient Activation Measurement (PAM)(Baseline, 4 and 12 months)
  • Cost- benefit(Baseline, 4 and 12 months)
  • Physical activity(Baseline, 4 and 12 months)
  • Use of medications(Baseline, 4 and 12 months)
  • fatigue (VAS scale)(Baseline, 4 and 12 months)
  • Pain (VAS scale)(Baseline, 4 and 12 months)
  • Arthritis Impact Measurement Scale 2 (affect, symptoms, social interaction, role)(Baseline, 4 and 12 months)
  • The Hospital Anxiety and Depression Scale(Baseline, 4 and 12 months)
  • Modified Health Assessment Questionnaire(Baseline, 4 and 12 months)
  • DAS 28 score (Disease activity score)(Baseline, 4 and 12 months)

Study Sites (1)

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