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NCT07499934Recruiting

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

Source: ClinicalTrials.gov · Last updated 30 Mar 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
20 (estimated)
First submitted
24 Mar 2026
Start date
19 Jan 2026
Primary completion date
19 Jan 2027
Lead sponsor
Centre Psychothérapique de Nancy
NCT number
NCT07499934

What you commit to

  • Study type: Interventional
  • Planned participants: 20
  • From 19 Jan 2026 to the primary completion date, 19 Jan 2027
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • \- Previous episode of schizophrenia, schizoaffective disorder, or bipolar disorder
  • Previous antipsychotic treatment for more than 12 months

Other illness

  • Organic mental disorder or intellectual disability

Other

  • 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

Who the study is looking for

  • 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)

Age in the registry: 15 years to 30 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Centre Psychothérapique de Nancy
Coordinator of this site? Confirm its status
LaxouFranceRecruiting
Clinique Fondation Santé des Etudiants de France
Coordinator of this site? Confirm its status
Vitry-le-FrançoisFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.