Comparing Mindfulness Based Cognitive Therapy and Mindfulness Based Self-compassion Therapy in a Psoriasis Sample
NCT ID: NCT02122978
Last Updated: 2014-04-25
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
94 participants
INTERVENTIONAL
2013-11-30
2015-05-31
Brief Summary
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The main research hypothesis is that participants who complete a mindfulness based intervention will experience significantly greater psychological well-being, symptom reduction, and greater changes in telomerase and cytokine activity than individuals who only receive treatment as usual for their psoriasis.
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Detailed Description
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Recruitment commenced in November 2013 and continued until March 2014. Participants were recruited via the Department of Dermatology in St. Vincent's University Hospital. During weekly dermatology clinics eligible participants were identified by medical members of the Dermatology team and on expression of interest were referred to an Assistant Psychologist for recruitment purposes. In addition participants were also recruited via an advertisement placed in a national newspaper.
Eligible patients will be randomly assigned to TAU (n=25), MBCT (n=25), MBSCT (n=25), or audio-guided MBSCT (n=25).
At Time 1 (pre intervention), participants will be required to give blood (a 50ml sample, i.e., roughly 10 teaspoons), and complete self-report measures on the same day as beginning the mindfulness programme. As it has previously been indicated that cells may be sensitive to sudden changes in stress, mood and time of day (Epel, 2012), blood samples will always be taken after completing the self-report measures and at a relatively standardized time, e.g., between 3-5pm. Care will be taken to ensure that conditions are relaxed across all participants, and a 10 minute rest period between completing the questionnaires and giving blood will be enforced. Bloods can be kept at room temperate for up to 24 hours and then prepared for storage below 60 degrees Celsius until PBMC analysis is to be conducted after all samples have been collected at Time 1 (post intervention).
At Time 2, six-months and twelve-months follow-up, participants will again be required to give 50ml of blood and complete all self-report measures via an identical protocol, and analysis will be conducted again accordingly. Telomerase will be assessed using a TRAPeze EXCEL Telomerase Detection Kit. This will be complemented by flow cytometry analysis of telomere length. Serum cytokines before and after treatment will be examined by ELISA. This should give an indication of the effect of treatment on systemic inflammation. We will also examine the ability of PBMC from patients to produce proinflammatory cytokines, including IL-6, TNF, IL-1, and others associated with anxiety and depression. PBMC will be activated with innate stimulus such as LPS/zymosan. The production of cytokines will be determined by ELISA. Highly sensitive CRP is also a marker for psoriasis and will be assessed by ELISA to give an indication of overall inflammation. In regards to self-report measures, the following psychological scales will be used:
1. Hospital Anxiety and Depression Scale (HADS; Snaith \& Zigmond, 1994)
2. Penn State Worry Questionnaire (PSWQ: Meyer, Miller, Metzger \& Borkovec, 1990) 3 Fears of Compassion Scales (Gilbert, 2009)
4\. Five Facets of Mindfulness Questionnaire (FFMQ: Baer, Smith, Hopkins, Krietemeyer \& Toner, 2006) 5. World Health Organisation Quality of Life - BREF (WHO, 2004). 6. Dermatology Quality of Life Index
Addressing our research question regarding the effectiveness of the mindfulness programs involves a repeated-measures comparative group intervention design. 4x4 mixed-methods ANOVAs will be used to assess pre, post and six/twelve month follow-up differences across the four experimental conditions, with group as the independent variable and psychological experience (e.g., depression, anxiety, worry, self compassion and mindfulness) or immunological activity (e.g., PBMC telomerase and cytokines) as the dependent variables. Number of hours per week practicing mindfulness during follow-up will be entered as a covariate. Effect sizes and confidence intervals will be calculated post-hoc using G\*Power in order to facilitate ease of comparison between the study findings and other future studies and the relevant field of literature. Bivariate Spearman's Correlations will be conducted to examine the relationship between psychological variables and telomerase and cytokine activity on all four testing occasions, respectively. Spearman's Correlations are chosen as a suitable non-parametric correlation analysis given reports of telomerase as non-normally distributed (e.g., Epel et al., 2010; Wolkowitz et al., 2012) and inspection of our own preliminary data.
Data will be collected on four occasions; pre and post intervention and at six and twelve months follow up.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
NONE
Study Groups
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Mindfulness Based Cognitive Therapy
Mindfulness Based Cognitive Therapy
Mindfulness Based Cognitive Therapy
MBCT 8 week course delivered by trained facilitator
MBSCT 8 week course
Mindfulness Based Self Compassion Therapy
Mindfulness Based Self Compassion Therapy
Mindfulness Based Self Compassion Therapy - 8 wee course delivered by trained facilitator
Mindfulness Based Self-Compassion - Audio guided
MBSC - minimal contact
MBSC - minimal contact
8 week course in Mindfulness Based Self Compassion delivered remotely by audio guided MP3
Interventions
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Mindfulness Based Cognitive Therapy
MBCT 8 week course delivered by trained facilitator
MBSC - minimal contact
8 week course in Mindfulness Based Self Compassion delivered remotely by audio guided MP3
Mindfulness Based Self Compassion Therapy
Mindfulness Based Self Compassion Therapy - 8 wee course delivered by trained facilitator
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* diagnosis of mild to severe psoriasis
Exclusion Criteria
* Participants deemed unsuitable for MBCT or MBSCT after a psychological assessment
* previous participation in a formal 8-week mindfulness programme (e.g., MBCT, MBSR).
18 Years
ALL
No
Sponsors
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St Vincent's University Hospital, Ireland
OTHER
Responsible Party
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Dr. Paul D'Alton
Dr. Paul D'Alton
Locations
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St. Vincent's University Hospital
Dublin, Dublin, Ireland
Countries
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Other Identifiers
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19/12/12 mind derm
Identifier Type: -
Identifier Source: org_study_id
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