Social Anxiety
Conditions
Keywords
health behaviour change, implementation intention, if then plan, skin condition, visible difference, self help
Brief summary
Individuals with visible conditions often report experiencing lowered social confidence and encountering intrusive reactions from others, yet relatively few targeted psychosocial self help interventions are available. The investigators will conduct a randomised controlled trial to compare the efficacy of an adapted form of an existing self-help intervention with an enhanced version of the same intervention that incorporates if-then planning instructions (or 'implementation intentions') and a control condition that will receive support as usual. Participants who self-identify as having a visible condition affecting the skin or hair, or scarring to the skin that negatively affects their social confidence will be allocated to one of three conditions: augmented self-help, standard self help or control. The interventions will be delivered online and participants will complete psychometric outcome measures at two time points, four weeks apart. It is hypothesised that participants who receive the augmented self help intervention will have a statistically significant decrease in fear of negative evaluation in comparison to both the standard self-help and support as usual control groups.
Detailed description
The proposed research will take the form of a randomised controlled trial conducted in accordance with CONSORT guidelines (http://www.consort-statement.org). Data will be collected online using Qualtrics. Participants will be required to answer all fields on Qualtrics, as a way of managing potential missing data. Participants will be randomly allocated to one of three groups: (i) psychological self-help augmented with implementation intentions, (ii) standard psychological self-help or (iii) a no intervention waiting list control. Qualtrics will be used to randomly allocate participants to one of the three groups. A sample size analysis has been conducted and calculated assuming two measures, three groups, an alpha of 0.05, a power of 0.8, and an effect size of 0.25; a total sample size of 120 participants would be needed (i.e. 40 per group). Allowing for an attrition rate of 20%, 144 participants would need to be recruited (i.e. 48 per group). Although participants will be randomised to condition, it is best practice for any differences at baseline to be controlled for in analyses and thus a between factors repeated measure analysis of variance (ANOVA) will be conducted.
Interventions
OTHERSelf help leaflet
Self help leaflet entitled 'Building confidence in social situations: A guide for people living with a visible skin differences'
Sponsors
University of Sheffield
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Participants self-identify as having a visible skin difference * Participants will be aged 18 years or over * Participants will be fluent in the English language
Exclusion criteria
Participants will be excluded if they are currently receiving psychotherapy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in Brief Fear of Negative Evaluation-II at four weeks (Carleton, Collimore, & Asmundson, 2007) | At baseline and four weeks |
Secondary
| Measure | Time frame |
|---|---|
| Change in Generalised Anxiety Disorder 7 at four weeks | At baseline and four weeks |
Other
| Measure | Time frame |
|---|---|
| Change in Patient Health Questionnaire 9 at four weeks | At baseline and four weeks |
Countries
United Kingdom
Outcome results
None listed