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Hello:
You are invited to participate in our survey which aims to explore the experience individuals with CFS/ME have using online support groups.
In this survey, you will be asked to complete questions about how you found the online groups you are a member of, how you use them, what you hope to get from them and what you find you do get from them. Some questions will be yes or no and using likert scales whilst others will provide space for you to type as much as you want. It will take approximately ? minutes to complete the questionnaire.
Your participation in this study is completely voluntary. There are no foreseeable risks associated with this project. However, if you feel uncomfortable answering any questions, you can withdraw from the survey at any point.
Your survey responses will be strictly confidential and data from this research will be reported anonymously. Your information will be coded and will remain confidential. If you have questions at any time about the survey or the procedures, you may contact Gerri Moxon, University of Hull, by email at the email address specified below.
Thank you very much for your time and support. If you are happy to participate in this research please start with the survey now by clicking on the Continue button below and tick the box to confirm you have read this information sheet.
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| Do you have a confirmed diagnosis of CFS or ME? |
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| How long have you had a confirmed diagnosis of CFS or ME? |
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| How long have you had the symptoms you experience? |
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