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Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.
Dr
Susan
Rasmussen
s.a.rasmussen@strath.ac.uk
Dr
Susan
Rasmussen
s.a.rasmussen@strath.ac.uk
This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.
This study aims to test the feasibility of a brief psychosocial intervention and to obtain pilot data to determine whether the administration of a postcard over a 6 month period (4 postcards in total) reduces self-harm, improves mood and decreases perceived defeat and entrapment in the short-term (6 months). We plan to use the effect sizes from this pilot study to inform the sample size calculations for a larger, more definitive trial.
Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.
The recruitment start and end dates are as follows:
Interventional type: Psychological & Behavioural;
You can take part if:
You may not be able to take part if:
(i) participants who are unfit for interview (as assessed by the psychiatric liaison team), (ii) those from whom we cannot gain informed consent, (iii) those who do not speak English as a first language, prisoners (given associated follow-up difficulties, and (iv) those of no fixed address (as the intervention involves sending postcards we are limited to individuals who do have a fixed address).
Below are the locations for where you can take part in the trial. Please note that not all sites may be open.
The study is sponsored by University of Strathclyde and funded by Scottish Government Chief Scientist Office (CSO) .
Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.
Read full details
for Trial ID: CPMS 9832
You can print or share the study information with your GP/healthcare provider or contact the research team directly.