Research call: Does neurofibromatosis affect how you feel about your body?
28 January 2021
Kate Adkins is a researcher and Trainee Clinical Psychologist based at the University of Sheffield. As part of her doctoral research, she is interested in improving self-help interventions for people living with neurofibromatosis and dermatological conditions.
If neurofibromatosis affects how you feel about your body, please consider helping psychologists test a 1-week online writing intervention. By taking part you will be helping us learn whether the intervention could help improve body image for other individuals living with a range of dermatological conditions and be in with a chance to win a £50 voucher of your choice.
Who can take part?
Anyone:
- Age 18 or over.
- Living with a condition that affects the skin (e.g. neurofibromatosis).
- Who feels their condition negatively impacts how they feel about their body.
- Able to read and write in English.
What will it involve?
You will be asked to complete three 15-minute online writing tasks over the course of a week. You will also be asked to complete several questionnaires before the first writing task, after the final writing task and one month later. As this is a randomised controlled trial, you will be randomly assigned to either: (1) the writing intervention or (2) a control writing task. If you are allocated to the control tasks, you will have access to the intervention material at the end of the study.
Please follow the link below to find out more.
Please contact Dr Kate Adkins (Trainee Clinical Psychologist, University of Sheffield) via k.adkins@sheffield.ac.uk for further information.
Filter News
![](https://nervetumours.org.uk/images/made/images/common/IMG_20230214_094714_370x280_800_600_s_c1.jpg)
Beth’s NF1 story
"I had no idea what NF was until I got diagnosed with it." Beth shares her NF1 journey to help raise awareness
Read More![](https://nervetumours.org.uk/images/made/images/common/WhatsApp_Image_2023-05-18_at_00.36.57_Front_370x280_800_600_s_c1.jpg)
Shine A Light 2023
The Shine A Light 2023 campaign had 162 buildings around the UK & the Republic of Ireland lit up in blue!
Read More![](https://nervetumours.org.uk/images/made/images/common/Christine_Grant__Margaret__Sheila__Maureen_370x280_800_600_s_c1.jpg)
Christine’s Coronation fundraising
Christine has been fundraising for NTUK for 10 years, since her grandson was diagnosed with NF1.
Read More![](https://nervetumours.org.uk/images/made/images/common/PXL_20220930_101710232_370x280_800_600_s_c1.jpg)
Megan’s NF1 story
Megan has NF1 & other complications: "I will always live my life to the fullest and not let my diagnosis stand in my way"
Read More![](https://nervetumours.org.uk/images/made/images/common/NTUK_Shine_A_Light_2023_website_banner_V2_370x280_800_600_s_c1.jpg)
Shine a Light May 2023
Shine A Light Activities during World NF Month May 2023 - Get Involved!
Read More![](https://nervetumours.org.uk/images/made/images/common/image1_(11)_370x280_800_600_s_c1.jpg)
Charlotte’s NF1 story
Charlotte and her brother & dad have NF1. She is running the Shine a Light Marathon during May to raise awareness
Read More![](https://nervetumours.org.uk/images/made/images/common/Screenshot_2023-05-10_174650_370x280_800_600_s_c1.jpg)
Be seen, be counted: #PicsForThe1in6
Be part of the Neurological Alliance's photo collage, representing people with neurological conditions
Read More![](https://nervetumours.org.uk/images/made/images/common/Sequentis_Health_NF1_PN_cover_370x280_800_600_s_c1.jpg)
Understand the experience of adults living with Neurofibromatosis Type I with Plexiform Neurofibromas (NF1 PN)
Research to understand the reality of the NF1 PN journey from diagnosis to daily life, and the emotional impact that has
Read More