Actively Recruiting

Phase Not Applicable
Age: 14Years - 30Years
All Genders
NCT07093671

Mentalization Based Treatment (MBT) in Help Seeking Youths With a Clinical High-Risk Condition for Psychosis (CHR-P)

Led by Marco Armando · Updated on 2025-11-25

212

Participants Needed

1

Research Sites

160 weeks

Total Duration

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AI-Summary

What this Trial Is About

The primary objective of this study is to evaluate the efficacy of Mentalization-Based Treatment (MBT) combined with Need-Based Clinical Interventions (NBCI) compared to NBCI alone, on CHR-P diagnostic statuses and symptom expression (Hypothesis 1). Specifically, the investigator will assess diagnostic outcomes using a 3-level variable: transition to psychosis, CHR-P status quo, and remission out of CHR-P, as well as CHR-P symptom expression. The investigator hypothesize that: (1a) the experimental treatment (MBT + NBCI) will have a significant effect on diagnostic status (i.e. transition to psychosis) at the end of treatment and follow-up; (1b) the experimental treatment (MBT + NBCI) will significantly reduce the severity of psychotic symptoms at the end of treatment and follow-up.

CONDITIONS

Official Title

Mentalization Based Treatment (MBT) in Help Seeking Youths With a Clinical High-Risk Condition for Psychosis (CHR-P)

Who Can Participate

Age: 14Years - 30Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 14-30 years with a CHR-P condition as defined by the SIPS criteria
  • Patients who provide informed consent
Not Eligible

You will not qualify if you...

  • Patients with a prior diagnosis of a psychotic disorder
  • Intellectual disability with IQ below 70
  • Psychotic symptoms primarily caused by substance misuse
  • Significant language barriers
  • Parents or legal guardians not providing consent for minors
  • Adult patients under guardianship

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

CHUV

Lausanne, Switzerland, 1011

Actively Recruiting

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Research Team

M

Marco Armando, Pr

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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