TITLE OF STUDY
Health perception within the positive health model and data exploitation
PRINCIPAL INVESTIGATORS
Mila Andreew
m.andreew@student.fontys.nl
Magnus Nystad
m.nystad@student.fontys.nl
PURPOSE OF STUDY
You are being asked to take part in a research study. Before you decide to participate in
this study, it is important that you understand why the research is being done and what it
will involve. Please read the following information carefully. Please ask the researcher if
there is anything that is not clear or if you need more information.
The purpose of this study is to address the need of people to see health as a more global
state of wellbeing. Furthermore, it will help us as student to apply the positive health
model concept in order to pinpoint potential behavior change needs.
STUDY PROCEDURES
The participant will fill in a 1st global questionnaire to create an overview of current
health.
From this, researchers will target specific points and create customized questions in order
to help participant define more specific objectives to improve previous results.
Researchers will ask for participant feedback on how this research helped them in seeing
and defining health specific objectives.
RISKS
You may decline to answer any or all questions and you may terminate your involvement
at any time if you choose.
BENEFITS
Participants will have the chance to learn more about their current overall well-being on
specific points and target specific points in order to improve it based on evidence-based
research.
CONFIDENTIALITY
For the purposes of this research study, your comments will not be anonymous. Every
effort will be made by the researcher to preserve your confidentiality including the
following:
• Keeping notes, interview transcriptions, and any other identifying participant
information in a locked file cabinet in the personal possession of the researcher.
Participant data will be kept confidential except in cases where the researcher is legally
obligated to report specific incidents. These incidents include, but may not be limited to,
incidents of abuse and suicide risk.
CONTACT INFORMATION
If you have questions at any time about this study, or you experience adverse effects as
the result of participating in this study, you may contact the researcher whose contact
information is provided on the first page.
VOLUNTARY PARTICIPATION
Your participation in this study is voluntary. It is up to you to decide whether or not to
take part in this study. If you decide to take part in this study, you will be asked to sign a
consent form. After you sign the consent form, you are still free to withdraw at any time
and without giving a reason. Withdrawing from this study will not affect the relationship
you have, if any, with the researcher. If you withdraw from the study before data
collection is completed, your data will be returned to you or destroyed.