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Clinical Trial ● Currently Recruiting Non-phase study NCT06568081

SloMo2: Implementation, Effectiveness, and Cost-effectiveness Study

SloMo2: Implementation, Effectiveness, and Cost-effectiveness Study — Recruiting • Non-phase study • Gastroenterology • NCT06568081.

📅 25 Mar 2026 ⏱ 3 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Non-phase study
NCT ID
NCT06568081
Sponsor
King's College London
Start
2024-10-16
ClinicaliQ Trial Snapshot
  • SloMo2: Implementation, Effectiveness, and Cost-effectiveness Study — Recruiting • Non-phase study • Gastroenterology • NCT06568081.
  • 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….
  • Sponsor: King's College London.

Verify eligibility, endpoints and current status on the original source registry before acting on this summary.

Use This Page For
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What This Trial Is Studying

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,…

Eligibility Snapshot
  • : * 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

Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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