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Future Mental Projections in Schizophrenia

Future Mental Projections in Schizophrenia

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03040505
Acronym
FutureProSchiz
Enrollment
56
Registered
2017-02-02
Start date
2017-04-05
Completion date
2019-10-20
Last updated
2023-08-23

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

Conditions

Schizophrenia

Brief summary

The aim of the study is to investigate temporal organization of future thinking in patients with schizophrenia. Patients and control participants will be asked to envision and briefly describe ten personal future events using a cue-words list. Then they will be asked to describe everything that came to their minds (i.e. to think aloud) while they attempted to determine when an event will likely occur. The investigators will compare the proportion of several predefined strategies mentioned by the two groups of participants to locate future events in time. The investigators predict that patients will envision less personal future events and will rely to a lesser extent on strategies to locate events in time, than control participants.

Interventions

Participant's verbalization will be audio recorded and then transcribed by investigators. The investigators will use predefined categories to score the strategies mentioned by participants during the think aloud task.

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* for patients only * male or female * age limits : 18-55 years old * under the protection of health insurance * who have signed up the consent form * schizophrenia or schizo-affective disorder according to the DSM-5 criteria (APA, 2013). * clinically stable for at least 2 months * patients under guardianship or curatorship need agreement of their legal representative * informed of the results of prior medical examination for controls only * male or female * age limits : 18-55 years old * under the protection of health insurance * who have sign up the consent form * recruited from the general population and matched on gender, age years of schooling * no psychiatric history (DSM-5)

Exclusion criteria

* for both patients and controls * current severe or unstable somatic illness * neurological history (brain injury \> 15 minutes loss of consciousness , epilepsia, brain surgery…) * current substance use disorder (DSM-5) * current major depressive disorder (CDSS,BDI, HDRS) * mental retardation (IQ \< 70, WAIS-4, f-NART) * history of general anesthesia 3 months prior to the experiment * pregnancy declared by the subject * breast feeding * current legal control * in emergency situation * included during exclusion period in another experiment * for controls only * taking of antipsychotic drugs for the 3 weeks prior to inclusion * under guardianship or curatorship

Design outcomes

Primary

MeasureTime frame
Number of time location strategies1 months

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026