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Cost Effectiveness of Two Different Strategies to Implement the NVOG Guideline Programme on Subfertility
The purpose of this study is to compare two different strategies to implement the existing Guideline programme on Subfertility, as issued by the Dutch Society of Obstetrics and Gynaecology (NVOG). Therefore, an innovative patient-directed strategy will be compared to a control strategy and effectiveness, costs and feasibility of both strategies will be assessed.
The Dutch Society of Obstetrics and Gynaecology (NVOG) has developed a guideline programme on Subfertility, including 9 guidelines concerning diagnosis and treatment of subfertility and a national IVF protocol. However, guidelines in general do not implement themselves; large gaps consists between best evidence (as described in the guidelines) and practice, resulting in a large variation between professionals. Our study will compare an innovative patient-directed strategy with a (minimal intervention) control strategy, and effectiveness, costs and feasibility of both will be assessed. We eventually aim at the most cost-effective strategy to implement the existing subfertility guideline programme. Please Note: In our protocol, we consider only 'couples' undergoing fertility treatment; therefore, we aim at gathering information from approximately 5200 records, of both male and female participants. When reporting eventually on their treatment, we will consider them only as couples, resulting in reported numbers of approximately 2600 participating couples.
Age
18 - 80 years
Sex
ALL
Healthy Volunteers
No
Jeroen Bosch Ziekenhuis
's-Hertogenbosch, Netherlands
Gelre Ziekenhuizen
Apeldoorn, Netherlands
Rijnstate Ziekenhuis
Arnhem, Netherlands
Maasziekenhuis Pantein
Boxmeer, Netherlands
ZBC stichting Geertgen
De Mortel, Netherlands
Slingeland Ziekenhuis
Doetinchem, Netherlands
Ziekenhuis Gelderse Vallei
Ede, Netherlands
Catharina Ziekenhuis
Eindhoven, Netherlands
st Antonius Ziekenhuis
Nieuwegein, Netherlands
Radboud University Nijmegen Medical Centre
Nijmegen, Netherlands
Start Date
October 1, 2005
Primary Completion Date
February 1, 2009
Completion Date
May 1, 2009
Last Updated
October 29, 2008
5,200
ESTIMATED participants
patient education
BEHAVIORAL
professional audit and feedback (guideline adherence)
BEHAVIORAL
professional education (communication/shared decision making)
BEHAVIORAL
information tools
OTHER
Lead Sponsor
Radboud University Medical Center
Collaborators
NCT06742437
NCT06921395
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06324071