Patient Outcome Study on Haemophilia - Join Now!
This high-profile Patient Outcome Study on Haemophilia aims to collect crucial data from doctors and patients to shape treatment guidelines and improve quality of life. Your participation will directly contribute to enhancing patient care and outcomes.
Download Presentation
Please find below an Image/Link to download the presentation.
The content on the website is provided AS IS for your information and personal use only. It may not be sold, licensed, or shared on other websites without obtaining consent from the author. If you encounter any issues during the download, it is possible that the publisher has removed the file from their server.
You are allowed to download the files provided on this website for personal or commercial use, subject to the condition that they are used lawfully. All files are the property of their respective owners.
The content on the website is provided AS IS for your information and personal use only. It may not be sold, licensed, or shared on other websites without obtaining consent from the author.
E N D
Presentation Transcript
Study Introduction Welcome To Our Patient Outcome Study about Haemophilia! Next Steps You have been specially invited to participate in a high profile Patient Outcome Study in Haemophilia It is a multi-phased study collecting data from both doctors and their patients (described in more detail on the next page) Study Background These studies are becoming increasingly important as pharmaceutical companies increase focus on patients and regulators look towards real world patient outcomes to support decisions They are also used to ensure the best possible treatment guidelines The data is typically published in peer-review journals, presented at key conferences and thus helps shape the treatment paths for sufferers and improve their lives Examples Quality of Life of Patients With Alzheimer s Disease presented at ISPOR 19th Annual European Congress (2016) Patient-reported Symptom Burden Among Relapsing-Remitting Multiple Sclerosis (RRMS) vs Secondary Progressive Multiple Sclerosis Patients (SPMS) in Europe presented at 1st Congress of the European Academy of Neurology Your and your patients feedback will directly lead to improvement in patients treatments and quality of life For more information about M3 Global Research click here
Study Design Phases step by step: Patient Pack posted to you by M3 Global Research 1. This recruitment process 2. A 5 minute online qualification survey 3. A 45 minute online survey Patient Record Forms* Qualification Survey Physician Survey M3 Global Research will then send you packs of survey materials for patients Recruitment 4. You complete a 15 - 25 minute patient record form for up to 8 patients as you see them 5 mins 45 mins 15 - 25 mins Patient 5. You ask these patients to complete a 20 minute questionnaire and return it to your receptionist for posting to M3 Global Research Self Completion Questionnaire* Online Paper 20 mins * These will be linked by three common questions; patients age band, gender and occupation plus a code unique to you. Neither will contain any patient identifiable information to protect the confidentiality of you and your patients.
Incentives Physician Survey* $ 100 Patient Pack posted to you by M3 Global Research 8 x Patient Record Forms ( 100 each)* $ 800 Bonus for 8 Patient Record Forms $100* $100 each* $ 100 Patient Record Forms Qualification Survey Physician Survey Recruitment Maximum Total $ 1,000 5 mins 45 mins 15 - 25 mins Patient Self Completion Questionnaire * A minimum of 3 Patient Record Forms are required to qualify for the Physician Survey incentive Online Paper 20 mins
