Skip to main content
Clinical Trials/NCT02733575
NCT02733575
Completed
Not Applicable

A Case Series Study of Compassion Focused Therapy for Distressing Experiences

King's College London1 site in 1 country9 target enrollmentSeptember 2015
ConditionsPsychosis

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Psychosis
Sponsor
King's College London
Enrollment
9
Locations
1
Primary Endpoint
Attrition rate measured by number dropping out of therapy
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

This study aims to develop and test the feasibility of a new therapy called Compassion Focused Therapy (CFT) for psychosis. This therapy helps people with psychosis manage distressing experiences by building internal feelings of safeness and affiliation, and by providing contexts, practices and insights that facilitate the development of compassion to self and others. The focus is on helping people feel safe in relation to their experiences and their social worlds. CFT is a promising new approach that has been successfully provided for people with a range of mental health difficulties. It is also firmly based in the most up-to-date knowledge and science about how the mind works (both normally and under stress).

9 participants will be recruited from NHS psychological therapies services for people with psychosis in South London and Maudsley (SLAM) NHS Foundation Trust. Following a short baseline period they will receive up to 26 weekly sessions (about 6 months) of CFT with a clinical psychologist, and will provide interview and questionnaire research data at five different points during the study. At these assessment points, data will be gathered on participants' experiences, mood, perceptions of their position in the social world, and heart rate variability.

The initial therapy protocol has been developed by psychologists with expertise in CFT, alongside people with lived experience of hearing voices and having distressing beliefs. However, it will continue to be developed and evolve as the study progresses, and as more is learnt (e.g. from the service-user participants) about applying the model in this population. At the end of this study, the aim is to have all the information needed to run a randomised controlled trial of this therapy.

Registry
clinicaltrials.gov
Start Date
September 2015
End Date
January 8, 2019
Last Updated
7 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Over 18 years old
  • Psychosis related diagnosis (F20-39)
  • Distressing positive symptoms of psychosis. Each participant will have been routinely screened with PSYRATS at their service entry assessment. On PSYRATS, at least one positive symptom (i.e. hallucination or delusion) will be present, and distress will be evidenced by an associated intensity score of 2 or above
  • Willing to engage in psychological therapy
  • Sufficient command of English language
  • Able to provide informed consent

Exclusion Criteria

  • Currently engaged in CBT, or have completed a 12+ session course of CBT within the last 3 years. If recruitment is under target, this will be relaxed to 12+ session course of CBT (Cognitive Behavioural Therapy) within the last 6 months
  • Currently engaged with another treatment study (e.g. medicine or therapy)

Outcomes

Primary Outcomes

Attrition rate measured by number dropping out of therapy

Time Frame: 6 months

Secondary Outcomes

  • Psychotic symptoms measured by PSYRATS(Over 6 months of therapy, and 6-8 weeks post-therapy)
  • Depression and anxiety symptoms measured by DASS-21(Over 6 months of therapy, and 6-8 weeks post-therapy)
  • Subjective wellbeing, symptoms, functioning, and risk/harm measured by CORE(Over 6 months of therapy, and 6-8 weeks post-therapy)
  • Dissociative experiences measured by DES-II(Over 6 months of therapy, and 6-8 weeks post-therapy)

Study Sites (1)

Loading locations...

Similar Trials