Co-investigator version of the protocol
Provides all the instructions for osteopaths contributing to the trial.
Please download the version for the country you are working from.
United Kingdom (UK)
Version 1.2 (UK)
Switzerland
English
French (Deepl translation in word format)
Australia (not yet available)
The full study plan complements the co-investigator version of the protocol and is made available for those who would like to consult it.
Recruitment form
These documents aim to inform potential participants of the trial. They can be distributed as planned by the protocol in each country.
For the UK
This support can be used to communicate about the study on social media or paper/electronic forms in the UK.
Recruitment Poster (UK)
For Switzerland
Please download the attached file in one of the three main national language. Complete the Word File with your specific details and make a PDF version of your own recruitment form. These can also be distributed by other health professionals to promote the study.
French version
German version
Italian version
English version
For Australia
This support can be used to communicate about the study on social media or paper/electronic forms in Australia.
Recruitment Poster (Australia)
Information and consent form
Potential participants receive a generic version of the information form at least 24h before their appointments. This word template is to be used to personalise the consent form. It needs to be completed and printed out for it to be used during the first appointments with potential participants.
For the UK
Participant information leaflet
Participant consent form
For Switzerland
French ICF
German ICF
Italian ICF
English ICF
For Australia
Participant information leaflet
Participant consent form
(Not available yet)
Template for log file
This document can serve as a template to record the number of people who have been asked to participate, reasons for refusals, and to log those that do enter the trial. The log file is the sole document that links the true ID of participants to their CASTOR ID. It is to be kept safely by co-investigators for at least ten years.
Questions from the CRF
This Excel file provides translations for all the content made available to participants.