- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01834313
Willingness to Pay for Patient-centred Care
July 22, 2013 updated by: A.G. Huppelschoten
Identifying Patients' and Healht Insurers' Preferences Regarding Patient-centred Care by Determining Their Willingness-to-pay for Patient-centred Care
The purpose of this study is to evaluate the monetary value of patient-centrednes in health care by determining a willingness-to-pay for more patient-centredness care for both patients and health insurers
Study Overview
Status
Unknown
Conditions
Detailed Description
We perform our study in the area of fertility care, as it is known that infertile patients suffer from a high physical and physiological burden during treatment and could especially benefit from patient-centred care.
Moreover, previous studies have clearly identified the concept of patient-centred fertility care and have shown that improvement is needed.
Study Type
Observational
Enrollment (Anticipated)
600
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Gelderland
-
Nijmegen, Gelderland, Netherlands, 6500 HB
- Recruiting
- Radboud University Medical Centre
-
Contact:
- W L Nelen
- Phone Number: 0031-24-3617350
- Email: w.nelen@obgyn.umcn.nl
-
-
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
- ADULT
- OLDER_ADULT
- CHILD
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Patient who are under treatment for their fertility problem and underwent at least one treatment in one of 10 Dutch clinics.
All healthcare purchasers from the 5 large Dutch health insurer companies
Description
Inclusion Criteria:
- Patients undergoing MAR-treatment (ovulation induction, intra-uterine inseminations, in vitro fertilization, or intra-cytoplasmic sperm injection)
- All healthcare purchasers working at one of the 5 large Dutch health insurer companies.
Exclusion Criteria:
- None
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Willingness-to-pay for patient-centred care
Time Frame: 6 months
|
A willingness-to-pay for patient-centred care for both patients and health insurers
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: J AM Kremer, MD, PhD, Radboud University Medical Centre, Nijmegen
- Study Director: W L Nelen, MD, PhD, Radboud University Medical Centre, Nijmegen
- Study Director: E MM Adang, PhD, Radboud University Medical Centre, Nijmegen
- Principal Investigator: A G Huppelschoten, MD, Radboud University Medical Centre, Nijmegen
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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 Major Dates
Study Start
November 1, 2012
Primary Completion (ANTICIPATED)
August 1, 2013
Study Completion (ANTICIPATED)
October 1, 2013
Study Registration Dates
First Submitted
April 12, 2013
First Submitted That Met QC Criteria
April 12, 2013
First Posted (ESTIMATE)
April 17, 2013
Study Record Updates
Last Update Posted (ESTIMATE)
July 23, 2013
Last Update Submitted That Met QC Criteria
July 22, 2013
Last Verified
July 1, 2013
More Information
Terms related to this study
Other Study ID Numbers
- DCE
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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