Feedback Reports and e-Learning in Primary Care Spirometry (FRESCO)
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ClinicalTrials.gov Identifier: NCT00962455 |
Recruitment Status :
Completed
First Posted : August 20, 2009
Last Update Posted : August 20, 2009
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Respiratory Tract Diseases Pulmonary Disease, Chronic Obstructive Asthma | Other: e-learning & performance feedback Other: usual practice | Phase 4 |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 1135 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Single (Outcomes Assessor) |
Official Title: | Feedback Reports and E-learning to Support Spirometry Test Performance in Dutch Family Practices |
Study Start Date : | November 2007 |
Actual Primary Completion Date : | November 2008 |
Actual Study Completion Date : | April 2009 |
Arm | Intervention/treatment |
---|---|
Experimental: e-learning & performance feedback
Initial e-learning by studying CD-Rom 'Spirometry Fundamentals', followed by repeated periodic performance feedback on spirometry test quality
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Other: e-learning & performance feedback
Initial e-learning by studying CD-Rom 'Spirometry Fundamentals', followed by repeated periodic performance feedback on spirometry test quality |
Active Comparator: Usual practice
Usual practice regarding spirometry execution in family practice
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Other: usual practice
Usual practice regarding spirometry execution in family practice |
- Proportion of spirometry tests with ≥2 acceptable blows according to 2005 ERS/ATS criteria that were also repeatable for both FEV1 and FVC [ Time Frame: 12 months prospective follow-up ]
- Proportions of tests with ≥2 acceptable blows according to 2005 ERS/ATS criteria [ Time Frame: 12 months prospective follow-up ]
- Proportions of spirometry tests with ≥2 blows meeting 2005 ERS/ATS end-of-test criteria [ Time Frame: 12 months prospective follow-up ]
- Proportions of spirometry tests with A to C grade according to scholastic-type quality grading system by Ferguson et al (2000) [ Time Frame: 12 months prospective follow-up ]
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Ages Eligible for Study: | 10 Years and older (Child, Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria for Family Practices:
- collaboration with Elkerliek Hospital Helmond through regional integrated care support service ('QUARTZ')
- purchased spirometer through this support service
- have implemented spirometry as a part of routine patient care
Inclusion Criteria for Patients:
- registered in one of the participating family practices
- performed a spirometry test as a part of routine care during the observation period of the study
Exclusion Criteria for Patients:
- age < 10 years
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00962455
Netherlands | |
Radboud University Nijmegen Medical Centre, Department of Primary and Community Care | |
Nijmegen, Netherlands, 6500 HB |
Principal Investigator: | Tjard R Schermer, PhD | Radboud University Medical Center | |
Principal Investigator: | Alan J Crockett, PhD | The University of Adelaide | |
Principal Investigator: | Willem Pieters, MD, PhD | Elkerliek Hospital |
Responsible Party: | Tjard Schermer, senior researcher, Radboud University Nijmegen MC, Dept of Primary and Community Care |
ClinicalTrials.gov Identifier: | NCT00962455 |
Other Study ID Numbers: |
UMCN-CARA-0001113 |
First Posted: | August 20, 2009 Key Record Dates |
Last Update Posted: | August 20, 2009 |
Last Verified: | August 2009 |
Spirometry Family Practice Randomized Controlled Trial Feedback Intervention Studies |
Pulmonary Disease, Chronic Obstructive Respiratory Tract Diseases Lung Diseases Chronic Disease |
Disease Attributes Pathologic Processes Lung Diseases, Obstructive |