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The Effectiveness of Mindfulness Based Cognitive Group Therapy for Social Anxiety Symptoms in People Living With Alopecia Areata

Not Applicable
Completed
Conditions
Alopecia Areata
Social Anxiety
Interventions
Behavioral: Mindfulness Based Cognitive Therapy
Registration Number
NCT03873155
Lead Sponsor
University of Sheffield
Brief Summary

This study investigates the impact of mindfulness based cognitive therapy (MBCT) on social anxiety in adults with alopecia areata. A single-group case-series design will be adopted.

Detailed Description

Alopecia areata (AA) is an immunological disorder which is characterised by round/oval patches of non-scarring hair loss. People living with AA are at higher risk of developing depression, anxiety and social phobia than the general population (Koo et al., 1994; Ruiz-Doblado, Carrizosa, \& García-Hernández, 2003). Interventions that aim to reduce engagement in negative appearance related thoughts, and attentional bias towards negative self-referential information may be helpful for this population.

Mindfulness-based cognitive therapy (MBCT) offers one potential method of reducing social anxiety in individuals with AA. MBC is a structured eight-week programme that has been recommended by the National Institute of Clinical Excellence as an effective intervention to reduce the risk of relapse in depression since 2009.

The main aim of the current study is to investigate whether an MBCT course can reduce social anxiety in individuals with AA. A single-group case-series design will be adopted, whereby participants will act as their own control; data collected from participants during and after they have received the intervention will be compared to data collected before they have received the intervention. Semi-structured interviews will be carried out at the end of the study to investigate participants experiences of the intervention.

The investigators predict that MBCT will reduce social anxiety in individuals with AA. More specifically, the hypothesis are:

(i) participants will experience an increase in mindfulness during the intervention period, relative to the baseline phase and this will be maintained at follow-up

(ii) increases in mindfulness will be associated with decreases in social anxiety, anxiety and depression, and increases in dermatology quality of life.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
6
Inclusion Criteria
  • AA is the main presenting physical health problem
  • Participant self-identifies as experiencing social anxiety
  • Sufficient English to participate in group sessions and discussion.
  • Aged 16 and over
Exclusion Criteria
  • Primary psychiatric diagnosis affecting skin (e.g., trichotillomania)
  • Hair loss as a result of medical intervention or surgery (e.g., chemotherapy)
  • The skin condition is secondary to other physical health problems (e.g., arthritis, cancer, chronic pain)
  • Patient does not report any social distress as a result of their AA
  • Currently undergoing other psychological therapy

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Mindfulness-based cognitive therapyMindfulness Based Cognitive TherapyThere is only one arm in this study. A range of variables will first be measured (daily and weekly) over a baseline period in a group of participants. Following this baseline period, participants will be take part in an MBCT intervention whilst the same variables are measured. Following the intervention,there will be a 4-week follow-up period, and MBCT groups will not run during this time.
Primary Outcome Measures
NameTimeMethod
Change in social anxiety (idiosyncratic measure)Daily for 20 weeks (baseline-intervention-follow-up)

The primary outcome measures for the proposed study are idiosyncratic measures of social anxiety which will be assessed daily by text message. Participants will be asked to identify one social anxiety-related positive target (something the participant would like to improve) and one negative target (something the participant would like to reduce). Participants will respond to the daily text messages with a score on a 0-100 scale

Secondary Outcome Measures
NameTimeMethod
Social AnxietyWeekly for 21 weeks (baseline-intervention-follow-up)

The Brief Fear of Negative Evaluation straight forward items (BFNE-S: Carleton, Collimore, McCabe, \& Antony, 2011) will be used to assess social anxiety. The measure consists of 8 questions rated on a 5-point Likert scale (from "not at all characteristic of me" to "entirely characteristic of me").

Depression4 time-points. Assessment (beginning of study) beginning of intervention (4 weeks later) end of intervention (9 weeks later) follow-up (8 weeks later)

The 9-item self-report Patient Health Questionnaire (PHQ-9; Spitzer, Kroenke, \& Williams, 1999) will be used to measure symptoms of depression. Items are rated on a four-point Likert scale (from "not at all" to "nearly every day").

Anxiety4 time-points. Assessment (beginning of study) beginning of intervention (4 weeks later) end of intervention (9 weeks later) follow-up (8 weeks later)

The Generalised Anxiety Disorder Questionnaire (GAD-7; Spitzer, Kronke, Williams, \& Lowe, 2006) is a 7 item self-report scale to measure generalized anxiety symptoms. Items are rated on a four-point Likert scale (from "not at all" to "nearly every day").

Quality of life (dermatology-related)4 time-points. Assessment (beginning of study) beginning of intervention (4 weeks later) end of intervention (9 weeks later) follow-up (8 weeks later)

The Dermatology Quality of Life Index (DLQI: Findlay \& Khan, 1994) consists of 10 questions concerning the impact of the skin condition over the last week. Questions relate to symptoms and feelings, daily activity, leisure, work/school, personal relationships and side effects of treatment. Items are rated on a 4-point Likert scale (from "not at all" to "very much").

Service use3-time points. 4 time-points. Beginning of intervention (4 weeks after assessment) end of intervention (9 weeks later) follow-up (8 weeks later)

The Client Service and Receipt Inventory (CSRI; Beecham \& Knapp, 2001) is a 6 question measure of client service utilization. More specifically, the CSRI measures how often participants have met with a healthcare professional, visited A \& E, been an inpatient, used an ambulance, received a diagnostic test, and days spent away from work due to ill health.

Mindfulness4 time-points. Assessment (beginning of study) beginning of intervention (4 weeks later) end of intervention (9 weeks later) follow-up (8 weeks later)

The Five Factor Mindfulness Questionnaire (FFMQ; Baer, Smith, Hopkins, Krietemeyer \& Toney, 2006) will also be used to measure mindfulness. Items are rated on a five-point Likert scale (from "never or very rarely true" to "very often or always true").

Work and social adjustment3-time points. 4 time-points. Beginning of intervention (4 weeks after assessment) end of intervention (9 weeks later) follow-up (8 weeks later)

The Work and Social Adjustment Scale (WSAS; Mundt \& Marks, 2002) is a 5-item measure of the impact of mental health issues on an individual's social life and ability to work.

Trial Locations

Locations (2)

Royal Hallamshire Hospital (Sheffield Teaching Hospital)

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Sheffield, South Yorkshire, United Kingdom

The University of Sheffield

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Sheffield, South Yorkshire, United Kingdom

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