Skip to main content
OpenTrials
Completed

NCT Number: NCT00879281

Action Plan to Enhance Self-management and Early Detection of Exacerbations in Chronic Obstructive Pulmonary Disease (COPD) Patients

The purpose of this randomized controlled trial is to evaluate the hypothesis that the 'written' action plan, a self-management tool developed by the project group, enhances early detection and prompt action measures and consequently isbeneficial in exacerbation outcome (i.e., health status recovery time).

Completed

Looking for future studies?

Notify Me

Key information

Age range

40 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht

Utrecht, 3584 CX, Netherlands

About this study

Early detection of exacerbations by COPD patients initiating prompt interventions has shown to be clinically relevant. Until now, research failed to identify the effectiveness of a written individualized Action Plan (AP) to achieve this. The current multicenter, single-blind RCT with a follow-up period of 6 months, evaluates the hypothesis that individualized AP's reduce exacerbation recovery time. Patients are included from regular respiratory nurse visits and allocated to either usual care or an additional AP providing individualized treatment prescriptions (pharmaceutical and non-pharmaceutical) related to a colour coded symptom status (reinforcement at 1 and 4 months). Although usually not possible in self-management trials, we ensured blinding of patients, using a modified informed consent procedure in which patients give consent to postponed information. Exacerbations in both study arms are defined using the Anthonisen symptom diary-card algorithm. The Clinical COPD Questionnaire (CCQ) is assessed every 3-days. CCQ-recovery time of an exacerbation is our primary outcome. Additionally, healthcare utilisation, anxiety, depression, treatment delay, and self-efficacy are assessed at baseline, 6 and 12 months.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • post-bronchodilator forced expiratory volume in 1 second/forced vital capacity (FEV1/FVC) ratio < 70%
  • age > 40 years
  • complaints of chronic cough
  • smoking history of more than 20 years or 15 pack-years
  • diagnosis of COPD as major functionally limiting disease and
  • current use of bronchodilator therapy.

Exclusion criteria

  • primary diagnosis of asthma
  • primary diagnosis of cardiac disease
  • presence of disease that could either effect mortality or participation in the study (e.g. confusional states).

Treatment and study plan

Action Plan

Behavioral

Individualized "written" Action Plan to enhance self-management and early detection of an exacerbation.

Primary outcomes

  1. CCQ-recovery time in the event of an exacerbation(Health status recovery time)

    Time frame: 6-months

Secondary outcomes

  1. Symptom recovery time in the event of an exacerbation

    Time frame: 6 months

  2. Health Related Quality of Life - St George Respiratory Questionnaire

    Time frame: baseline and 6 months follow-up

  3. The Hospital Anxiety and Depression Scale (HADS)

    Time frame: baseline and 6 months follow-up

  4. Medical Research Council (MRC) Dyspnoea Scale

    Time frame: baseline and 6 months follow-up

  5. Julius Self-Efficacy Scale

    Time frame: baseline and 6 months follow-up

  6. Contact delay & treatment delay in the event of an exacerbation

    Time frame: 6 months

  7. Exacerbation rates (Number of symptom-based / event-based exacerbations per patient year)

    Time frame: 6 months

  8. Healthcare Utilization (The number of respiratory-related hospital admissions, hospital days, emergency room visits and scheduled and unscheduled visits or telephone calls to a RP and GP)

    Time frame: 6 months

Sponsors and collaborators

Lead sponsor

UMC Utrecht

Other

Registry information

Official study title

Action Plan to Enhance Self-management and Early Detection of Exacerbations in COPD Patients; A Multicenter RCT (ACZiE)

Acronym: ACZiE

Important dates

Study start
2008
Primary completion
2010
Study completion
2010
First posted
Apr 9, 2009
Registry last updated
Feb 24, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.