Experience of UHR and PEP Individuals During Mindfulness: a Qualitative Phenomenological Study
Recruiting
N/A
Interventional Study
Clinical High Risk for Psychosis (CHR)
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 15 – 30
- Sex
- Any
- Study type
- Interventional
- Purpose
- Other
- Participants needed
- 20 (estimated)
- Sponsor
- Centre Psychothérapique de Nancy · Other
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About This Trial
The goal of this qualitative study is to explore and describe the lived experiences of individuals at ultra-high risk (UHR) or first episode of psychosis (FEP) who have participated in a group-based mindfulness-based intervention. Secondary objectives include identifying potential adverse effects of a group-based mindfulness-based intervention among UHR or FEP.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* People aged between 15 and 30 years who meet the criteria for UHR or PEP status on the CAARMS scale and have a social functional impact (SOFAS score less than 50 or a decrease of more than 30% in the score)
Exclusion Criteria:
* \- Previous episode of schizophrenia, schizoaf…
Contacts