Experience of UHR and PEP Individuals During Mindfulness: a Qualitative Phenomenological Study
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age15-30
SponsorCentre Psychothérapique de Nancy
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.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
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)
Disqualifiers
- Previous episode of schizophrenia, schizoaffective disorder, or bipolar disorder
Previous antipsychotic treatment for more than 12 months
Organic mental disorder or intellectual disability
Serious suicide/homicidal risk (but admissible if this risk has been resolved)
Trial design
Design model
Single group
Treatments tested in this trial
Qualitative interview
Other interventionanalysis of interview data using the IPSE (Inductive Process to analyze the Structure of lived Experience) method
Treatment groups
20 Participants
are divided into 1 treatment groupGroup A: Qualitative interviewOther 1 intervention
Trial outcomes
Primary outcomes
1
Lived experiences
To explore and describe the lived experiences of individuals with UHR or FEP who have participated in a group-based mindfulness intervention using the IPSE method.
Time frame
The qualitative interview takes place between one week and three months after the final session of the mindfulness-based programSponsors and contacts
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Source ClinicalTrials.gov