Status:

COMPLETED

Dissociation CBT Studies

Lead Sponsor:

University of Birmingham

Conditions:

Dissociation

Depersonalization

Eligibility:

All Genders

16-80 years

Phase:

NA

Brief Summary

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...

Detailed Description

1. What is dissociation? "I was in a totally different world; it was going on all around me. I thought that I might have died and was in hell, and I was thinking maybe that's what it was." -- "Mar...

Eligibility Criteria

Inclusion

  • 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 ČEFSA-14 (i.e., 39 or above); Černis 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

  • 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.

Key Trial Info

Start Date :

September 20 2023

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

March 12 2025

Estimated Enrollment :

9 Patients enrolled

Trial Details

Trial ID

NCT06054009

Start Date

September 20 2023

End Date

March 12 2025

Last Update

July 3 2025

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Birmingham Womens and Childrens NHS Foundation Trust

Birmingham, United Kingdom