- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01054677
Swedish Antibiotic Nursing Home Trial (SANT)
January 21, 2010 updated by: Karolinska Institutet
Main aim and objective
The aim was to present the treatment of infectious diseases in elderly, especially in nursing homes and further to evaluate the effect of an intervention package aiming at improving treatment with antibiotics in Swedish nursing homes
Specific objectives
- Present the treatment patterns regarding infectious diseases, including gender aspects in elderly, especially in nursing homes.
- Through focus group discussions elucidate the decision making process in nursing homes and target the intervention.
- Based on the above information develop an educational intervention to contribute to the improvement of the prescribing of antibiotics in nursing homes
- Evaluate the effect of the intervention on quality of prescribing, knowledge and attitudes in relation to available guidelines
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Phase
- Not Applicable
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
N/A
Description
Inclusion Criteria:
- nursing homes where residents have a common dining room and staff, and a self-assessed stable staff situation
Exclusion Criteria:
- specialised nursing homes or wards (e.g. oncology wards)
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Educational intervention on antibiotic prescribing
The participants in this group received an educational intervention.
|
Small educational group sessions with nurses and physicians, feedback on prescribing, presentation of guidelines and written materials
|
|
No Intervention: No educational intervention
The participants in this group did not receive the educational intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Registration Dates
First Submitted
January 21, 2010
First Submitted That Met QC Criteria
January 21, 2010
First Posted (Estimate)
January 22, 2010
Study Record Updates
Last Update Posted (Estimate)
January 22, 2010
Last Update Submitted That Met QC Criteria
January 21, 2010
Last Verified
May 1, 2003
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- dnr 03-070
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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