Professionals Feedback Questionnaire

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Thank you for taking the time to watch the video series on supporting the communication development of deaf babies and toddlers; a resource for families. We would now like to get an idea of how you feel about the videos so we have a few questions to ask you. Please note that your responses are anonymous and will be stored and reported as such. This means that no personal identifying information will be collected.

This research has been approved by the Psychology Department's Ethics Committee at the University of Sheffield (reference number 030430).

You can take part in this research if you are:

- A professional who directly supports families who have a deaf/hearing impaired child/children
- A stakeholder in the Deaf community
- Over 18

What is the purpose of the study?

We would like to know how acceptable and helpful you find the videos to be. We are also asking caregivers of young children with any level of hearing loss for the same information.

What is involved if I agree to take part?

This questionnaire is mobile enabled and will take approximately 10-30 minutes to complete. Once you have started the questionnaire it isn’t possible to return and complete it at a later date, so responses need to be started and submitted in a single sitting. If you do not click ‘submit’, then your responses will not be recorded. Your responses will be collected, stored and reported in anonymous format. This means that no personal identifying information will be collected.

What if I change my mind?

If you start the questionnaire but change your mind, you can simply close your browser to stop taking part in the study. This will automatically delete all of your responses. There are no consequences for not completing the survey. After you have submitted your responses to the questionnaire, it will not be possible to withdraw your data, because it is anonymous and so we will not be able to identify your responses.

Is the information I provide anonymous?

The questionnaires are anonymous and will not include your name. Once questionnaires are completed online, the data can only be accessed by the researchers.

Are there any risks involved in taking part?

Although the risk is low, it is possible that you may feel distressed when thinking about support for families. If this is the case, please contact your GP for support.

What are the benefits of taking part?

The benefit of taking part is to help to develop effective support for families.

What if I have any further questions, or have any problems?

If you have any questions about completing this questionnaire, please contact Dr Danielle Matthews (Project Lead) at danielle.matthews@sheffield.ac.uk.

What if I want to complain about this research?

If you would like to make a complaint, please contact Dr Thomas Webb at t.webb@sheffield.ac.uk.

I have read and understood the above information *

Yes

I agree with this information and hereby give my consent to take part in the study. *

By selecting “Yes I agree and hereby give my informed consent”, you are confirming that you: (1) are over the age of 18; (2) understand the nature of this questionnaire; (3) understand that taking part is entirely your choice, without consequence; (4) understand what will happen to your data; and (5) fully consent to participate

Yes

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