Acute Respiratory Tract Infections Monitoring and Evaluation Study
| ISRCTN | ISRCTN57824788 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN57824788 |
| ClinicalTrials.gov (NCT) | NCT00105248 |
| Protocol serial number | N/A |
| Sponsor | University Hospital Basel (Switzerland) |
| Funders | Swiss National Science Foundation (Switzerland) (ref: 3200B0-102137), Novartis Foundation (Switzerland) (ref: 04B29) |
- Submission date
- 04/04/2005
- Registration date
- 21/04/2005
- Last edited
- 10/11/2008
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Respiratory
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Plain English summary of protocol
Not provided at time of registration
Contact information
Prof Heiner C Bucher
Scientific
Scientific
Basel Institute for Clinical Epidemiology
University Hospital Basel
Hebelstr. 10
Basel
4031
Switzerland
Study information
| Primary study design | Interventional |
|---|---|
| Study design | Randomised controlled trial |
| Secondary study design | Randomised controlled trial |
| Scientific title | Patient centred communication training to reduce antibiotic use in acute respiratory tract infections |
| Study acronym | ARTIMES |
| Study objectives | The purpose of this study is to evaluate the effectiveness of a short training program for general practitioners in patient-centered communication to reduce antibiotic prescription for acute respiratory tract infections (ARTI). |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Acute respiratory tract infection |
| Intervention | Patient centred communication training and evidence-based guidelines versus evidence-based guidelines. |
| Intervention type | Other |
| Primary outcome measure(s) |
Up-take of antibiotic prescription confirmed by pharmacists within 2 weeks following the initial consultation |
| Key secondary outcome measure(s) |
1. Patient satisfaction with consultation (on validated scale) |
| Completion date | 30/11/2004 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Adult |
| Lower age limit | 18 Years |
| Sex | All |
| Target sample size at registration | 900 |
| Key inclusion criteria | General practitioners were randomised and recruited adult patients with acute respiratory tract infections Inclusion criteria: 1. 18 years or older 2. Symptoms of an acute repiratory tract infection for greater than 1 and less than 28 days |
| Key exclusion criteria | 1. Patients without informed consent 2. Not fluent in German 3. Patients with a psychiatric disorder 4. Patients with a recurrent respiratory system infection with antibiotic treatment in the previous 4 weeks |
| Date of first enrolment | 01/01/2004 |
| Date of final enrolment | 30/11/2004 |
Locations
Countries of recruitment
- Switzerland
Study participating centre
Basel Institute for Clinical Epidemiology
Basel
4031
Switzerland
4031
Switzerland
Results and Publications
| Individual participant data (IPD) Intention to share | No |
|---|---|
| IPD sharing plan summary | |
| IPD sharing plan |
Study outputs
| Output type | Details | Date created | Date added | Peer reviewed? | Patient-facing? |
|---|---|---|---|---|---|
| Results article | results (communication training) | 15/04/2006 | Yes | No | |
| Results article | results (prevalence and influence of diagnostic tests) | 15/04/2006 | Yes | No |