Respiratory Tract Infections Clinical Trial
— ISAAC-CATOfficial title:
Effectiveness and Cost-effectiveness of Improving Clinicians' Diagnostic and Communication Skills on Antibiotic Prescribing Appropriateness in Patients With Acute Cough in Primary Care in Catalonia.
Despite their marginal benefit, about 60% of uncomplicated acute lower respiratory infections (ALRTI) are currently treated with antibiotics. Several strategies have been developed to reduce inappropriate antibiotic prescribing, with the use of point-of-care C-reactive protein (CRP) testing and the improvement of the communication skills being the most effective interventions, but most of the studies have been carried out outside Mediterranean countries. This study is aimed at evaluating the effect of a disease-focused intervention (CRP) and an illness-focused intervention (improvement of communication skills to optimise doctor-patient consultations and share-decision making with the aid of patient-centred leaflets) on antibiotic prescribing for patients with ALRTIs in Catalan primary care by means of a cluster, randomised, factorial, controlled trial. Primary care centres will be assigned to four trial arms: usual care, use of CRP testing, enhanced communication skills backed up with leaflets, or combined interventions. The main outcome will be antibiotic use within the first 6 weeks and the quality adjusted life years. A pharmacoeconomic analysis of the impact of these interventions will be assessed.
Status | Not yet recruiting |
Enrollment | 2940 |
Est. completion date | December 31, 2021 |
Est. primary completion date | February 28, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - age equal or older than 18 years - first consultation for acute cough (new cough or worsening of a previous cough) as the predominant symptom - of up to 3 weeks' duration - which the clinician believes to be an infectious acute lower respiratory tract infection Exclusion Criteria: - a working diagnosis of a non-infective disorder, such as heart failure, pulmonary embolus, oesophageal reflux, or allergy - use of antibiotics in the previous two weeks - immunological deficiencies, and/or - inability to provide informed consent or unable to follow the study procedures |
Country | Name | City | State |
---|---|---|---|
Spain | La Marina Health Center | Barcelona | Catalonia |
Lead Sponsor | Collaborator |
---|---|
Jordi Gol i Gurina Foundation | Fundacio d'Atencio Primaria, Universitat Internacional de Catalunya, Universitat Pompeu Fabra |
Spain,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Antibiotic use | Number of antibiotics consumed (as documented in the CRFs and double-checked by the Pharmacy Unit of Institut Català de Salut that can track if the antibiotic has been dispensed at any of the Catalan pharmacies) | Day 42 | |
Primary | Health status | Quality of life score obtained using the EuroQol questionnaire | Difference between baseline visit and day 42 | |
Secondary | Re-consultations and complications | Number of re-consultation for new or worsening symptoms, new signs, or hospital admission, assessed by review of medical notes (practice staff, the local study team, or both using a standard form to report these data), and Number of complications regarding the ALRTI | Day 42 | |
Secondary | Duration of symptoms and duration of severe symptoms | Number of days until symptoms are rated daily as 0 (no problem) (information is reported by patients in self-completed diaries) | Day 42 | |
Secondary | Antibiotic prescription at the baseline visit | Number of antibiotic prescriptions at the baseline visit, differentiating immediate and delayed antibiotic prescribing, and antibiotic dispensing at the pharmacies | Baseline visit | |
Secondary | Drugs other than antibiotics | Number of non-antibiotic prescriptions (reported by patients in self-completed diaries) | Day 42 | |
Secondary | Tests ordered by clinicians | Number of tests ordered by clinicians (reported in the CRF) | Day 42 | |
Secondary | Patient satisfaction with care | Patient satisfaction score reported in the symptom diary. Measured with a question that has used in previous studies: How satisfied are you with the consultation? Range from 0 (nothing satisfied) to 5 (extremely satisfied). | Day 14 | |
Secondary | Patient perception of the usefulness of the information received. | Patient perception score about the usefulness of the information received. Measured with a question that has used in previous studies: Do you consider that the information received from your doctor has been useful? Range from 0 (nothing useful) to 5 (extremely useful). | Day 14 | |
Secondary | Patient future consulting intention | Patient future consulting intention score. Measured with a question that has used in previous studies: Do you think you will attend the doctor in future occasions in case you present the same symptoms? Range from 0 (totally unlikely) to 5 (sure). | Day 14 | |
Secondary | Serious adverse events | Number of serious adverse events (assessed by review of medical notes (practice staff, the local study team, or both using a standard form to report these data) | Day 42 | |
Secondary | Absenteeism | Number of days of sick leave (collected in the CRFs) | Baseline visit |
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