PRIME goal is to early detect and treat acute exacerbations of chronic obstructive pulmonary disease (AECOPD). This is important since COPD accelerates aging and represents major burden worldwide and in Portugal, mainly due to its frequent AECOPD. Pulmonary rehabilitation (PR) is an effective strategy of its management but it is scarce. When AECOPD are early detected and treated, it optimizes patients' outcomes and reduces the burden of COPD, especially if PR is used. However, up to date, there is no model to predict AECOPD for clinical practice. The lung microbiota shows promise to overcome this barrier and inform on COPD trajectory and will be investigated. In addition, despite of most AECOPD being managed in the community, PR is mainly available in hospitals and less than 1% of patients are having access. Thus, community-based PR will be implemented and a clinical decision tool developed for prioritizing who will most benefit from PR, enhancing evidence-based access to PR.
PRIME aims to address these two gaps, establishing the role of microbiota and clinical data in predicting AECOPD and increasing the evidence on PR in AECOPD through the translation of PR guidelines to the community. Specifically, it aims to: * Explore the longitudinal changes in microbiota and clinical data between stable and exacerbations periods; * Establish the feasibility and short- and long-term effects of community-based PR for AECOPD; * Define the characteristics of patients who most benefit from community-based PR. 156 patients with COPD will be followed monthly for a year and their lung microbiota and clinical data will be analysed. Community-based PR will be delivered to 56 patients. Data will be collected before, at 3 weeks, after PR and at 6 months to assess the feasibility and effects of PR. A clinical decision-making tool (CDMT) to prioritise patients with AECOPD for PR will be developed. The experienced multidisciplinary team will ensure the following novel results: * a clinical and lung microbiota profile of patients with COPD; * a model of AECOPD prediction; * recommendations for community-based PR in AECOPD; * a CDMT to prioritise patients with AECOPD for PR. PRIME will contribute to optimise outcomes, improve AECOPD healthcare services and reduce the burden with COPD.
Study Type
INTERVENTIONAL
Purpose
TREATMENT
Masking
NONE
Enrollment
156
Pulmonary rehabilitation will be provided to patients presenting an acute exacerbation. The intervention will be composed of exercise training, education and psychosocial support.
University of Aveiro
Aveiro, Portugal
RECRUITINGChange in exercise tolerance
exercise tolerance in a walking field test
Time frame: Up to 6 months
Change in lung microbiota
lung microbiota from saliva samples
Time frame: Up to 6 months
Change in muscle strength
Upper and lower limb muscle strength
Time frame: Up to 6 months
Change in health related Quality of life
Measured with the St. George's Respiratory Questionnaire, that measures health related quality of life. It will be used the total score. Scores are expressed as a percentage of overall impairment where 100 represents worst possible health status and 0 indicates best possible health status.
Time frame: Up to 6 months
Change in resting dyspnoea
Resting dyspnoea measured with the modified British medical research council dyspnoea questionnaire, that ranges from 0 to 4, and is related to dyspnoea during activities of daily living. Higher scores demonstrate a higher functional impairment due to dyspnoea.
Time frame: Up to 6 months
Change in self-efficacy
self-efficacy measured with the pulmonary rehabilitation adapted index of self-efficacy tool
Time frame: Up to 6 months
Change in physical activity
Physical activity levels measured with the brief physical activity assessment tool
Time frame: Up to 6 months
Change in lung function
Lung function will be assessed through spirometry to define the airflow limitation (FEV1pp).
Time frame: Up to 6 months
Change in emergency department visits
Number of emergency visits on the previous year
Time frame: Up to 6 months
Change in frequency of exacerbations
Number of exacerbations on previous year
Time frame: Up to 6 months
Change in hospitalizations
Number of hospitalizations on previous year
Time frame: Up to 6 months
Dyspnoea during exercise
Dyspnoea experienced during exercise, monitored with the modified Borg dyspnoea scale, that ranges from 0 to 10, where 0 represents no dyspnoea and 10 the worst imaginable dyspnoea.
Time frame: Up to 6 months
Fatigue during exercise
Fatigue experienced during exercise, monitored with the modified Borg dyspnoea scale, that ranges from 0 to 10, where 0 represents no fatigue and 10 the worst fatigue the patient can imagine.
Time frame: Up to 6 months
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