Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06568081

SloMo2: Implementation, Effectiveness, and Cost-effectiveness Study

Led by King's College London · Updated on 2026-01-26

150

Participants Needed

1

Research Sites

167 weeks

Total Duration

On this page

Sponsors

K

King's College London

Lead Sponsor

S

South London and Maudsley NHS Foundation Trust

Collaborating Sponsor

AI-Summary

What this Trial Is About

Worries about harm from others (also known as paranoia) are common. Thinking fast or going on gut feelings is natural but can fuel these worries. For some, fast thinking and worries start to get in the way of life. Cognitive behaviour therapy for psychosis (CBTp) is the recommended talking therapy. However, only a minority of people can access CBTp due to limited resources, and even when available, therapy can be difficult to do and use in daily life. SloMo is a digitally supported therapy that aims to overcome these barriers, and was developed by people with psychosis, designers, and psychologists. It supports people to notice worries and fast thinking habits. During therapy sessions, people learn to slow down and feel safer. Personalised spinning thought bubbles are slowed down using SloMo tips. An app provides access to helpful messages. SloMo was previously tested in a randomised trial of 361 people attending mental health services. SloMo was found to be safe to use, with no adverse events linked to the software. People in the SloMo group had lower paranoia, and better confidence and wellbeing, over 6 months compared to people who just received their usual care. People found SloMo enjoyable and easy to use. The next step is to evaluate if SloMo can be safely and effectively delivered by therapists working in NHS services. If SloMo works in routine care, the therapy will be made more widely available in the NHS. An improved version of SloMo has been co-produced based on feedback. Sixty therapists will be trained and supervised in 3 trusts to deliver SloMo to 150 people who fear harm from others. Safety, technical performance, uptake, engagement and acceptability data, alongside interviews with patients, therapists, and managers, will investigate how SloMo is used. Paranoia severity and wellbeing will be measured pre, post therapy, and at 12 months follow up, to find out if SloMo helps. Service use data will evaluate costs and savings.

CONDITIONS

Official Title

SloMo2: Implementation, Effectiveness, and Cost-effectiveness Study

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Meet criteria for ICD-10 psychosis diagnoses (F20-29, F30-39)
  • Seeking therapy for paranoia
  • In contact with secondary care mental health services
  • Capacity to provide informed consent to engage in therapy
Not Eligible

You will not qualify if you...

  • Acute risk of harm to self or others
  • Unable to engage in therapy due to language barriers
  • Primary diagnosis of alcohol/substance dependence, learning disability, or organic brain injury or illness implicated in psychosis

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

South London and Maudsley NHS Foundation Trust

London, United Kingdom

Actively Recruiting

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Research Team

K

Kathryn M Taylor

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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