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Clinical Trials/NCT00705302
NCT00705302CompletedNot Applicable

A Randomised Controlled Trial of the Effect of a Patient Education Program for Patients With Chronic Obstructive Pulmonary Disease (COPD)

Norwegian University of Science and Technology2 sites in 1 country88 target enrollmentStarted: September 2007Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
88
Locations
2
Primary Endpoint
St. George's Respiratory Questionnaire (SGRQ) - Total score

Study Overview

Brief Summary

The aim of this study is to determine the long term effect of a self-help group in a patient education program for patients with chronic obstructive pulmonary disease (COPD).

Detailed Description

Pulmonary rehabilitation is aimed to increase the level of health of patients with COPD by increasing their self care ability. A recent updated systematic review concluded that evidence strongly supports respiratory rehabilitation as part of the spectrum of management of patients with chronic obstructive pulmonary disease (COPD). Studies of pulmonary rehabilitation programs lasting up to 18 months show that effects are mainly maintained throughout the duration of the program. The long term effect, however, is mostly studied for programs of shorter durations. Some of the studies with shorter duration have found that the achieved benefit was lost or diminished during the follow up period, while others have found that the effect has been maintained up to 18 months. Our necessity in the rehabilitative field is to find strategies to maintain benefits during time.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

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

Inclusion Criteria

  • (FEV1) lower that 75% of predicted
  • the ability to participate in physical activity
  • not been hospitalized the last month.

Exclusion Criteria

  • contraindications for physical activity

Outcomes

Primary Outcomes

St. George's Respiratory Questionnaire (SGRQ) - Total score

Time Frame: Baseline, 3, 6 and 12 months

Secondary Outcomes

  • Patient Activation Measure (PAM)(Baseline, 3, 6 and 12 months)
  • The Perceived Quality of Life Scale(Baseline, 3, 6 and 12 months)
  • 6 minute walk test (6MWT)(Baseline, 3, 6 and 12 months)
  • Modified Borg scale (MBS) pre, during and post 6MWT(Baseline, 3, 6 and 12 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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