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Clinical Trials/NCT00326222
NCT00326222CompletedNot Applicable

Patient Education in NorthTrondelag Hospital Trust - Interventions, Effects and Patient Experience

Norwegian University of Science and Technology2 sites in 1 country146 target enrollmentStarted: May 2006Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
146
Locations
2
Primary Endpoint
PAM - Patient activation measure

Study Overview

Brief Summary

The purpose of this randomised open study is to examine the effect of self-management program for diabetes patients.

Detailed Description

The primary aim in this study is HbA1c in addition to secondary aims like quality of life and coping.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Masking
None

Eligibility Criteria

Ages
18 Years to 90 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Diagnosed with ICPC-2, code T89 - diabetes dependent on insulin and T90 diabetes not dependent on insulin

Exclusion Criteria

  • Diagnosed with ICPC-2, code T89 - diabetes mellitus juvenile and diabetes I
  • Attended self-management program previous 12 months

Outcomes

Primary Outcomes

PAM - Patient activation measure

Time Frame: Baseline, 6, and 12 mds

HbA1c

Time Frame: Baseline, 6, and 12 mds

Secondary Outcomes

  • SF36(Baseline, 6, and 12 mds)
  • EQ 5D-VAS scale(Baseline, 6, and 12 mds)
  • Hunt diabetes(Baseline, 6, and 12 mds)
  • Knowledge of diabetes(Baseline, 6, and 12 mds)
  • Cost/benefit(Baseline, 6, and 12 mds)
  • Triglyceride(Baseline, 6, and 12 mds)
  • WHO-DTSQ(Baseline, 6, and 12 mds)
  • HDL-cholesterol(Baseline, 6, and 12 mds)
  • Creatinin(Baseline, 6, and 12 mds)
  • Blood pressure(Baseline, 6, and 12 mds)
  • BMI(Baseline, 6, and 12 mds)
  • Total cholesterol(Baseline, 6, and 12 mds)
  • Weight(Baseline, 6, and 12 mds)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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