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NCT07645443
FEEL-GOOD: A Multicenter Trial of a Mindfulness-Based Group Therapy in Young Adults With Early Psychosis
Conditions: Early Onset Psychosis, First Psychotic Episode Within the Last 5 Years, First-episode Psychosis, Schizophrenia Spectrum Disorders (SSD), Psychosis, Psychosis NOS, Randomized Controlled Trial (RCT)
Sex: All
Ages: 16 Years – 35 Years
Healthy volunteers: No
Phase: NA
Enrollment: 252
Sponsor: Stephanie Mehl
Location: University of Mannheim, Central Institute of Mental Health, Department of Psychiatry and Psychotherapy, J5, 68169 Mannheim Mannheim Baden-Wurttemberg
Summary
FEEL-GOOD is a prospective multi-site single-blinded randomized controlled trial in young inpatients with acute early psychosis. Participants are randomized 1:1 to FEEL-GOOD plus treatment as usual (TAU) or TAU alone. The intervention consists of one individual preparatory session and eight modularized group sessions delivered over four weeks involving four to eight participants at each session and including practice and homework tasks. Outcomes are assessed at baseline, 4 weeks post-intervention, and 6 months follow-up, with the primary outcome being observer-rated total psychopathology as measured with the assessed by the total score of the Positive and Negative Syndrome Scale (PANSS) post-treatment (4 weeks post baseline).
Eligibility Criteria
Inclusion Criteria:
* Age 16 to 35 years
* Clinical diagnosis of early psychosis, defined as first psychotic episode within the last 5 years as assessed with the Structural Clinical Interview for DSM-5 Research Version (SCID-5-RV)
* DSM-5 schizophrenia spectrum or other psychotic disorder confirmed with SCID-5-RV (DSM-5: 297.1, 298.8, 295.4, 295.9, 295.7, 298.8, 298.9) Currently receiving inpatient/day clinic treatment with a planned stay of at least 4 weeks
* Interested in and willing to participate in FEEL-GOOD and/or TAU.
Exclusion Criteria:
* Insufficient German language abilities
* Acute suicidality or acute threat to others
Source: ClinicalTrials.gov (NCT07645443). StuddyBuddy aggregates publicly available trial information.