Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht
Utrecht, 3584 CX, Netherlands
NCT Number: NCT00879281
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).
Looking for future studies?
Notify Me40 year and older
All sexes
Interventional
Not applicable
Utrecht, 3584 CX, Netherlands
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Individualized "written" Action Plan to enhance self-management and early detection of an exacerbation.
Time frame: 6-months
Time frame: 6 months
Time frame: baseline and 6 months follow-up
Time frame: baseline and 6 months follow-up
Time frame: baseline and 6 months follow-up
Time frame: baseline and 6 months follow-up
Time frame: 6 months
Time frame: 6 months
Time frame: 6 months
UMC Utrecht
Other
Action Plan to Enhance Self-management and Early Detection of Exacerbations in COPD Patients; A Multicenter RCT (ACZiE)
Acronym: ACZiE
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.
NCT05610514
Asthma, Asthma-COPD Overlap Syndrome
Burlington, Vermont, United States
View Trial DetailsNCT02895152
Bronchial Diseases, Bronchitis
Salford, Greater Manchester, United Kingdom
View Trial DetailsNCT00298389
Bronchial Diseases, Bronchitis
London, United Kingdom
View Trial DetailsNCT02951312
Bronchial Diseases, Bronchitis
View Trial Details