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Reality-monitoring & Stress

Study acronym: REALIST
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated July 24, 2025 (before its estimated October 25, 2025 completion). Its status may not reflect the trial's current state.

Record History

  1. Primary completion date: Jan 16, 2025 to Oct 25, 2025v8
  2. Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 1
    • Start date changed from estimate of Apr 30, 2024 to Apr 25, 2024
    v7
  3. Start date: Oct 15, 2023 to Apr 30, 2024v6
  4. Start date: Jul 15, 2023 to Oct 15, 2023v5
  5. Start date: Apr 15, 2023 to Jul 15, 2023v4
Show 2 earlier versionsHide 2 earlier versions
  1. Primary completion date: Jan 16, 2023 to Jan 16, 2025
    • Start date: Jan 15, 2023 to Apr 15, 2023
    v3
  2. Start date: Nov 15, 2022 to Jan 15, 2023
    • Primary completion date: Nov 16, 2022 to Jan 16, 2023
    v2
  1. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Reality-monitoring is a crucial cognitive process in daily life to remember the source of an information. Deficits of reality-monitoring have been shown into the continuum of schizophrenia, suggesting a preexisting alteration in population at-risk for psychosis that will be exacerbated during psychotic transition. It is admitted that stress plays a crucial role in the psychotic transition and can alter cognitive performances. However, less is known about the effects of stress on reality-monitoring, even though this process appears to be central in psychotic disorders. The aim of this project is to investigate the effect of stress on reality-monitoring, both on behavioral and neurophysiological aspects
Trial Details
NCT Number NCT05595434
Lead Sponsor Hôpital le Vinatier
Conditions
(from sponsor)		 Healthy Participants
Enrollment 40 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov