Compassion Focused Therapy for Distressing Experiences

Sponsor
King's College London (Other)
Overall Status
Completed
CT.gov ID
NCT02733575
Collaborator
(none)
9
1
1
40.2
0.2

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Compassion Focused Therapy
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
9 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
A Case Series Study of Compassion Focused Therapy for Distressing Experiences
Study Start Date :
Sep 1, 2015
Actual Primary Completion Date :
Jan 8, 2019
Actual Study Completion Date :
Jan 8, 2019

Arms and Interventions

Arm Intervention/Treatment
Other: Compassion Focused Therapy

Intervention

Other: Compassion Focused Therapy
Up to 26 sessions of Compassion Focused Therapy

Outcome Measures

Primary Outcome Measures

  1. Attrition rate measured by number dropping out of therapy [6 months]

Secondary Outcome Measures

  1. Psychotic symptoms measured by PSYRATS [Over 6 months of therapy, and 6-8 weeks post-therapy]

    Measured by PSYRATS (Psychotic Symptom Rating Scales)

  2. Depression and anxiety symptoms measured by DASS-21 [Over 6 months of therapy, and 6-8 weeks post-therapy]

    Measured by DASS-21 (Depression, Anxiety and Stress Scale)

  3. Subjective wellbeing, symptoms, functioning, and risk/harm measured by CORE [Over 6 months of therapy, and 6-8 weeks post-therapy]

    Measured by CORE (Clinical Outcomes in Routine Evaluation)

  4. Dissociative experiences measured by DES-II [Over 6 months of therapy, and 6-8 weeks post-therapy]

    Measured by DES-II (Dissociative Experiences Scale)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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)

Contacts and Locations

Locations

Site City State Country Postal Code
1 South London and Maudsley NHS Foundation Trust London United Kingdom

Sponsors and Collaborators

  • King's College London

Investigators

  • Principal Investigator: Charlie Heriot-Maitland, DClinPsych, King's College London

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
King's College London
ClinicalTrials.gov Identifier:
NCT02733575
Other Study ID Numbers:
  • R&D2018/024
First Posted:
Apr 11, 2016
Last Update Posted:
Mar 15, 2019
Last Verified:
Mar 1, 2019
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 15, 2019