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Chronic Obstructive Pulmonary Disease (COPD) frequently coexists with other diseases. Whereas COPD action plans are currently part of usual care, they are less suitable and potentially unsafe for use in the presence of comorbidities. This study evaluates whether an innovative treatment approach directed towards COPD and frequently existing comorbidities can reduce COPD exacerbation days. We hypothesise that this approach, which combines self-initiated action plans and nurse support, will accelerate proper treatment actions and lead to better control of deteriorating symptoms.In this multicenter randomised controlled trial we aim to include 300 patients with COPD (GOLD II-IV), and with at least one comorbidity (cardiovascular disease, diabetes, anxiety and/or depression). Patients will be recruited from hospitals in the Netherlands (n = 150) and Australia (n = 150) and will be assigned to an intervention or control group. All patients will learn to complete daily symptom diaries for 12-months. Intervention group patients will participate in self-management training sessions to learn the use of individualised action plans for COPD and comorbidities, linked to the diary. The primary outcome is the number of COPD exacerbation days. Secondary outcomes include hospitalisations, quality of life, self-efficacy, adherence, patient's satisfaction and confidence, health care use and cost data.Intention-to-treat analyses (random effect negative binomial regression and random effect mixed models) and cost-effectiveness analyses will be performed.Prudence should be employed before extrapolating the use of COPD specific action plans in patients with comorbidities. This study evaluates the efficacy of tailored action plans for both COPD and common comorbidities.

作者:Anke, Lenferink;Peter, Frith;Paul, van der Valk;Julie, Buckman;Ruth, Sladek;Paul, Cafarella;Job, van der Palen;Tanja, Effing

来源:Contemporary clinical trials 2013 年 36卷 1期

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作者:
Anke, Lenferink;Peter, Frith;Paul, van der Valk;Julie, Buckman;Ruth, Sladek;Paul, Cafarella;Job, van der Palen;Tanja, Effing
来源:
Contemporary clinical trials 2013 年 36卷 1期
标签:
AD AR-DRG Australian refined diagnosis related groups BODE CAT CCMP COPD COPD Assessment Test COPD Self-Efficacy Scale CRQ CSES Chronic Obstructive Pulmonary Disease Chronic Respiratory Questionnaire Clinical protocols Comorbidity Comprehensive Care Management Program DSMB Data Safety Monitoring Board EQ VAS EQ-5D ESC EuroQol Visual Analogue Scale EuroQol-5 dimensions European Society of Cardiology FEV(1) FEV(6) FVC GOLD GP HADS HL HbA1c Health Literacy Hemoglobin A1c Hospital Anxiety and Depression Scale ICFS Identity-Consequence Fatigue Score MBS MMSE Medicare Benefits Schedule Mini Mental State Examination PAS PBS Partners in Health Pharmaceutical Benefit Scheme PiH Randomized controlled trial Research design SD Self care anxiety and/or depression body mass index, obstruction, dyspnoea, exercise capacity forced (expiratory) vital capacity forced expiratory volume in one second forced expiratory volume in six seconds general practitioner global initiative for chronic obstructive lung disease mMRC modified Medical Research Council patient activation status standard deviation
Chronic Obstructive Pulmonary Disease (COPD) frequently coexists with other diseases. Whereas COPD action plans are currently part of usual care, they are less suitable and potentially unsafe for use in the presence of comorbidities. This study evaluates whether an innovative treatment approach directed towards COPD and frequently existing comorbidities can reduce COPD exacerbation days. We hypothesise that this approach, which combines self-initiated action plans and nurse support, will accelerate proper treatment actions and lead to better control of deteriorating symptoms.In this multicenter randomised controlled trial we aim to include 300 patients with COPD (GOLD II-IV), and with at least one comorbidity (cardiovascular disease, diabetes, anxiety and/or depression). Patients will be recruited from hospitals in the Netherlands (n = 150) and Australia (n = 150) and will be assigned to an intervention or control group. All patients will learn to complete daily symptom diaries for 12-months. Intervention group patients will participate in self-management training sessions to learn the use of individualised action plans for COPD and comorbidities, linked to the diary. The primary outcome is the number of COPD exacerbation days. Secondary outcomes include hospitalisations, quality of life, self-efficacy, adherence, patient's satisfaction and confidence, health care use and cost data.Intention-to-treat analyses (random effect negative binomial regression and random effect mixed models) and cost-effectiveness analyses will be performed.Prudence should be employed before extrapolating the use of COPD specific action plans in patients with comorbidities. This study evaluates the efficacy of tailored action plans for both COPD and common comorbidities.