Act it Out Prototype App Trial
20 August 2020
Researchers from the Centre for Appearance Research at UWE Bristol are looking for people with NF who are experiencing psychological / social difficulties related to looking different or ‘visible difference’, to test ACT It Out, a prototype mobile app.
ACT It Out
has been designed to help its users do more of the things they care about in life, and to reduce the impact of appearance concerns on their daily life.
![](/images/common/ACT_It_Out_logo__tagline1024x768.png)
UWE Bristol would like to understand what it is like to use ACT It Out: specifically, how helpful it is, how much participants like using it, and if it is doing what it is designed to do.
The app programme, “ACT It Out”, is a 6-session course, based on an established psychological approach called Acceptance and Commitment Therapy (ACT). It has been co-designed by UWE Bristol researchers together with people who have visible differences and charities (led by Vitiligo Support UK), specialist psychologists (led by Dr Olivia Donnelly from North Bristol NHS Trust) and mobile app experts.
For more information and to register your interest please visit go uwe.ac.uk/ACTItOutInterest Thank you!
![](/images/made/images/common/Act_it_out_members_1200x900_800_300_s_c1.png)
It is designed as a ‘low-level’ intervention, meaning it is self-guided and does not involve real-time support from health professionals. ACT It Out is not designed to take the place of professional face-to-face talking therapies, and is not intended for people experiencing serious mental health difficulties. It has a reading age of 12+.
UWE Bristol have now finished producing a prototype mobile app (using the Qualtrics® platform), which we are ready to pilot with up to 40 adults with visible differences. They are very keen to recruit participants with a wide range of appearance-affecting conditions, including NF.
Who can take part?
You can take part if you:
- Are aged 18 or older AND
- Are based in the UK AND
- Have a visible difference AND
- Are experiencing psychological and/or social difficulties to do with concerns about your visible difference. Common difficulties are social anxiety and/or withdrawal from social activities, receiving unwelcome attention from others, low mood, low self-esteem, body image concerns; (you may experience one, a few, or all of these difficulties) AND
- Own a smartphone (Apple, Android or Windows) with enough data allowance and/or Wi-Fi to regularly access the internet AND
- Have experience using smartphone apps AND
- Are able and willing, in principle, to commit to completing (a) six weekly sessions, each lasting around 30-mins (though they can be done in pieces) and (b) brief activities between each session (2-10-mins daily). Taking part does not mean you have to complete the entire course as completion is entirely voluntary
Unfortunately, because of who ACT It Out is designed for, you are not be eligible to take part if you:
- Have developed a visible difference as the result of a traumatic injury in the past 6 months OR
- Are experiencing marked distress / a mental health crisis, such as psychological trauma, severe low mood, suicidal thoughts, self-harm, or are feeling disconnected from reality OR
- Are currently going through any talking therapy or expect to be within the next 3 months OR
- Your primary appearance concerns are to do with weight and/or eating.
By getting involved with the Act it Out prototype you may experience benefits to your own personal psychological and/or social benefits to your daily life. Not only that you will help the app become more widely available, potentially helping many others around the world who have a ‘visible difference’ to get specialist help.
If you are interested and would like more information, please email Fabio.zucchelli@uwe.ac.uk or call Fabio on 0117 32 83882 (9am-5pm Monday-Friday).
Nerve Tumours UK is not responsible for any data collection or content of the project.
Filter News
![](https://nervetumours.org.uk/images/made/images/common/inform_your_GP_370x280_800_600_s_c1.jpg)
Resources Survey: Initial Diagnosis 2023
We received many responses to our survey asking what would you have found helpful after your initial diagnosis
Read More![](https://nervetumours.org.uk/images/made/images/common/Karen__NF_Community_370x280_1_800_600_s_c1.jpg)
Community Fundraising Call Out
Calling all community fundraisers - we need your help, please!
Read More![](https://nervetumours.org.uk/images/made/images/common/Awareness_Day_group_photo_370x280_800_600_s_c1.jpg)
Owen family Awareness Event
The event featured guest speaker Prof. Meena Upadhyaya OBE, Member of our Board of Trustees & Medical Advisory Board
Read More![](https://nervetumours.org.uk/images/made/images/common/Wilbur_370x280_800_600_s_c1.jpg)
Running for Wilbur
Tim is running the Guildford 10k in October, to show support to his son Wilbur who has NF1
Read More![](https://nervetumours.org.uk/images/made/images/common/Alice_Allsop_370x280_800_600_s_c1.jpg)
Alice’s NF studies
Alice is researching healthcare experiences of individuals with NF1 for her Genetic & Genomic Counselling MSc
Read More![](https://nervetumours.org.uk/images/made/images/common/CAR_parent_toolkit_1_370x280_800_600_s_c1.jpg)
Centre for Appearance Research - The Parenting Toolkit
Research evaluation to find out how effective ‘The Parenting Toolkit’ is at supporting parents of children with NF
Read More![](https://nervetumours.org.uk/images/made/images/common/848d9823-65f9-42e7-8ae9-e7ab055a62ba_(2)_370x280_800_600_s_c1.jpg)
Celtic Crossing NTUK fundraiser
On Wednesday 28 June, a team of 8, led by Paul Aubery, paddled from the Isles of Scilly to Sennen Cove in Cornwall.
Read More![](https://nervetumours.org.uk/images/made/images/common/IMG_6261_370x280_800_600_s_c1.jpg)
NF Awareness Day Fundraiser at Fyling Hall School
Bea's school held a blue & green themed fundraiser on World NF Awareness Day
Read More![](https://nervetumours.org.uk/images/made/images/common/image_(2)_370x280_800_600_s_c1.jpg)
Eden Study
Investigating early social, communication and attention development in babies who have NF1/ or a parent has NF1
Read More