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Experience of UHR and PEP Individuals During Mindfulness: a Qualitative Phenomenological Study

Experience of UHR and PEP Individuals During Mindfulness: a Qualitative Phenomenological Study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07499934
Acronym
EMIP
Enrollment
20
Registered
2026-03-30
Start date
2026-01-19
Completion date
2027-07-19
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Clinical High Risk for Psychosis (CHR)

Keywords

Psychosis, mindfulness

Brief summary

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.

Interventions

OTHERQualitative interview

analysis of interview data using the IPSE (Inductive Process to analyze the Structure of lived Experience) method

Sponsors

Centre Psychothérapique de Nancy
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
15 Years to 30 Years
Healthy volunteers
No

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, 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) * Insufficient French language skills * Adult unable to give consent and not under legal guardianship * Protective measure (guardianship/conservatorship/judicial protection) or under judicial supervision * Person deprived of liberty by judicial or administrative decision (including actual involuntary hospitalization) * Persons in a life-threatening emergency * Not affiliated with a social security scheme * Minors without parental authorization * Person who refused the audio recording of the interview

Design outcomes

Primary

MeasureTime frameDescription
Lived experiencesThe qualitative interview takes place between one week and three months after the final session of the mindfulness-based programTo 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.

Countries

France

Contacts

CONTACTWilliam DALFIN, MD
william.dalfin@cpn-laxou.com+33 3 83 92 68 22
CONTACTNaoual MELLOUKI BENDIMRED, PhD
unic@cpn-laxou.com0383925267
PRINCIPAL_INVESTIGATORwilliam DALFIN

Centre Psychothérapique de Nancy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 31, 2026