Public Consultation – high-risk soft tissue sarcoma

Public Consultation – high-risk soft tissue sarcoma

Patient group input requested for a new Collaborative Assessment on a medical device for high-risk soft tissue sarcoma

EUnetHTA deems patient involvement very important in the production of Collaborative Assessment reports We recognise that patients and those who support them have unique knowledge about what it is like to live with a specific disease or medical condition. We believe patient groups can help us understand patients’ unique perspectives by collecting and presenting patients’ and carers/care-givers’ views and experiences by engaging with a wide range of patients. They can describe advantages and disadvantages of medical treatments based on patients’ experiences and what patients value from a new treatment.

EUnetHTA recently started a new Collaborative Assessment on a medical device for the treatment of high-risk soft tissue sarcoma. For this specific assessment, an ‘open call for patient group submission‘ is used. We are seeking for European and national patient organisations to provide an organisational perspective on the questions in English[1]. In all parts of this form the term “patient” refers to anyone living with, or who has lived with, the condition for which the new medical device is indicated. The information provided will inform the scope of the assessment, e.g. on patient relevant outcomes or possible neglected outcomes, as well as on the burden of disease.

The questions in this call are taken from the HTAi questionnaire template. For more information on the development of the HTAi questionnaire template please see their website.

EUnetHTA strives to be transparent in the information used and at the same time we recognise that completing this form requires substantial resources. Therefore, we commit ourselves to making all patient submissions publically available at our webpage, at the timing of publication of the project plan for this assessment. In due course, this can be found here. Of course, we will anonymise the data from individual patients prior to publication. Furthermore, our Collaborative Assessment report will document how the information from patients was considered in developing the scope of our EUnetHTA Collaborative Assessment.

If you are interested in submitting information, please go to the questionnaire below and submit your input before

Please see below for further guidance on how to complete this questionnaire. If you have any questions when completing this form, please contact EUnetHTA Joint Production lead partner, the Norwegian Institute of Public Health at WP4.LP_EUnetHTA.JA3@fhi.no

CONSULTATION CLOSED

Patient group input – high-risk soft tissue sarcoma
Many thanks for your valuable input!

[1] We are working on translation the questionnaire to national languages, so that also individual patients can submit information. Unfortunately, this will not be possible for this specific assessment on a medical device for high-risk soft tissue sarcoma.

Your Information

We use Crowdsignal to collect information. Crowdsignal has created a GDPR Access Tool to help owners of quizzes, polls and other surveys with GDPR information access requests from respondents to their polls, surveys and quizzes.

This tool allows respondents to look up and request deletion of information about their responses and related personal information. Delete requests are accompanied by your email address and country where you are making the request.

A cookie is used to keep you logged into this page. It holds a randomly generated string that is also recorded on our servers. It expires within an hour unless you navigate around this page.

If, after reviewing your information, you’d like to request that your information be deleted, Crowdsignal will pass on your request to us. Your email address is part of the response and will be sent too. You should reach out to us for any further inquiries about your personal information or responses.

Your IP address indicates you are making this request from inside the EU.

Review your submission HERE

This website uses cookies to ensure you get the best experience on our website. By using the website you agree to our Privacy Policy and our Terms of Use.