PARROT Patient Information
What will my child and I have to do if we take part?
If you decide you would like your child to be involved in the trial you will be asked to read and sign a consent form.
After you have looked at the information on this website, and if you have no more questions and have decided you would like your child to take part in the trial, then you will be asked to read and sign a consent form to confirm this in writing.
You will be given a copy of the consent form and the information on this website to keep. Once you have signed the consent form, you will be asked some questions about your child’s respiratory health and we will check that the trial remains suitable for your child before starting treatment and following the trial plan.
Before your child’s treatment is dispensed, we will collect some other information about them, including medical history, recent vaccinations, current medications and school attendance.
We will also measure their weight, ask you to complete some questionnaires and may take a nasal swab. Once your child’s trial treatment is dispensed, you will go home and complete the sleep assessment(s). After this has been completed your child will start their treatment at home. The treatment will be given once daily every Monday, Wednesday and Friday.
azithromycin or placebo
Your child will receive either 12 months of azithromycin or placebo.
During this time, we will be in touch with you each month to ask how your child is getting on and if, for example, they have been to see their GP. Usually this will be by phone or email, however, every 3 months this will be by face-to-face so we can provide you with more of your child’s treatment, answer some questionnaires, obtain your child’s weight and may take a nasal swab. Your research team will try to make these face-to-face follow ups as easy as possible for you, for example, by arranging them at the same time as your normal clinic visits where possible.
At the 12-month follow up visit, your child will stop trial treatment and return to the standard treatment at their hospital.
There may be an additional face-to-face follow up visit at 20 months, which will follow a similar format as the other face-to-face follow up visits. Your research team will be able to tell you more about whether your child will take part in this additional visit.
Answering the questions and completing questionnaires will take about 15 minutes each time.
The questions include how your child is getting on and the questionnaires will ask about yours, and your child’s, sleep and quality of life.
We will weigh your child at the start of the trial and at each face-to-face follow up visit.
In addition, if your child visits their hospital outside of the arranged follow up visits due to a chest infection we will also collect some information about this visit and we may take some nasal swabs