Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT06703827

Effects of Online Metacognitive Training Group on Distressing Beliefs

Led by City, University of London · Updated on 2024-11-25

72

Participants Needed

1

Research Sites

74 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Psychosis is characterized by distorted perceptions of reality, often involving persecutory delusions. Research links these symptoms to cognitive biases like "jumping to conclusions." Despite mixed reviews of Cognitive Behavioral Therapy (CBTp) for psychosis, a study will explore metacognitive training (MCT) delivered online. This training will be tested over 10 weeks with participants from a psychosis service in Kent, assessing its effect through interviews and questionnaires before and after the program, focusing on symptom improvement and cognitive changes.

CONDITIONS

Official Title

Effects of Online Metacognitive Training Group on Distressing Beliefs

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of first episode of psychosis, schizophrenia spectrum, or affective disorder with psychotic symptoms
  • Score of 3 or above on the PANSS delusions scale
  • Age between 18 and 65 years
  • Able to speak and read English
Not Eligible

You will not qualify if you...

  • Currently admitted as an inpatient
  • Under 18 years of age
  • Moderate to severe learning disability
  • Severe organic impairment
  • Severe substance use disorder
  • Unable to speak and write English fluently
  • Currently participating in another interventional research study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Kent and Medway NHS and Social Care Partnership Trust

Maidstone, Kent, United Kingdom, ME16 9PH

Actively Recruiting

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Research Team

K

Kasia Mrs Wawrzyniak

CONTACT

A

Anne-Kathrin Fett, Dr

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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