Dissociation Clinical Trial
— DisCSOfficial title:
Treating 'Felt Sense of Anomaly'-Type Dissociative Experiences by Targeting Hypothesised Psychological Maintenance Mechanisms: A Single Case Experimental Design Series
Dissociation involves distressing feelings of unreality and disconnection. Evidence suggests it is particularly common amongst people with existing mental health difficulties, where it has been linked with greater clinical severity, poorer treatment response, and increased self-harm and suicidality. However, there are currently no psychological treatments for dissociation that have been developed from a scientific understanding of its underpinning psychological factors. In this project, three studies, each with four participants, will test a different psychological factor. Participants will be: adults (16+ years); on a waiting list for NHS psychological therapy; high scorers on a dissociation questionnaire. Participants will complete assessments before and after treatment, and at a one-month follow-up. The studies follow a 'multiple baseline design', meaning that all four participants for that study will complete their baseline assessment in the same week, and then be randomly allocated to wait either one, two, three, or four weeks before starting the intervention. The intervention will consist of four therapy sessions taking place within a five-week 'window'. Taking part in the research is voluntary. Before deciding whether to participate, we will explain the study and answer any questions. Daily, participants will record a score for their dissociation and the psychological factor being targeted. At baseline, post-therapy, and follow-up, the researchers will also measure their levels of other factors related to dissociation (i.e. those not targeted by the therapy). Additionally, feedback will be requested from participants about the therapy at the end of their involvement, in order to improve it in future. Ultimately, if successful, these interventions could form a pilot therapy for further testing and development. This could mean fewer people struggle with the challenges of dissociation.
Status | Recruiting |
Enrollment | 12 |
Est. completion date | September 2024 |
Est. primary completion date | September 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 16 Years to 80 Years |
Eligibility | Inclusion Criteria: - Aged between 16 years to 80 years; - Outpatient of UK mental health services (at the time of referral to the study); - Experiencing significant levels of 'felt sense of anomaly'-type dissociation (defined as a score within the 'moderately severe' or 'severe' range on the CEFSA-14 (i.e., 39 or above); Cernis et al., in prep.); - Want help to improve their dissociative experiences; - Willing and able to give consent for participation in the study; - Available to undertake the baseline assessment in the indicated week; - Available to undertake the therapy sessions within the indicated therapy 'window'. Exclusion Criteria: The participant may not enter the study if ANY of the following apply: - Diagnosis of an Axis II ("personality") disorder; - Primary diagnosis of alcohol/substance dependency, organic syndrome, or learning disability; - Presence of risk issues that would be a clinical priority above managing dissociative symptoms (e.g., moderate to severe self-harm; active suicidal behaviour; etc.); - Current engagement in any other individual psychological therapy (or psychological therapy due to begin within the participation window for this study). - A participant may also not enter the study if there is another factor (i.e., with higher clinical priority), which, in the judgement of the investigator, would preclude the participant from providing informed consent or from safely engaging with the study procedures. |
Country | Name | City | State |
---|---|---|---|
United Kingdom | Birmingham Womens and Childrens NHS Foundation Trust | Birmingham |
Lead Sponsor | Collaborator |
---|---|
University of Birmingham |
United Kingdom,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Acceptability of therapy and study to participants | Qualitative feedback (written or verbal) | Through study completion, average of 3 months | |
Primary | Study 1: Cognitive Appraisals of Dissociation | Visual Analogue Scale (0-100 rating) for cognitive appraisals of dissociation (higher scores = worse outcome) | Through study completion, average of 3 months | |
Primary | Study 2: Perseverative Thinking | Visual Analogue Scale (0-100 rating) for cognitive appraisals of perseverative thinking (higher scores = worse outcome) | Through study completion, average of 3 months | |
Primary | Study 3: Affect intolerance | Visual Analogue Scale (0-100 rating) for affect intolerance (higher scores = worse outcome) | Through study completion, average of 3 months | |
Secondary | Levels of dissociative experience (felt sense of anomaly subtype dissociation) | Visual Analogue Scale (0-100 rating) for FSA-dissociation (higher scores = worse outcome) | Through study completion, average of 3 months |
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