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NCT04325100: Switch

Intervention Targeting Motivational Negative Symptoms

Completed NA Last updated 27 March 2020
What this trial tests

NA trial testing Switch - Individual sessions in Schizophrenia in 13 participants. Completed in 27 February 2020.

Timeline
20 April 2019
Primary endpoint
6 December 2019
27 February 2020

Quick facts

Lead sponsorUniversity of Liege
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment13
Start date20 April 2019
Primary completion6 December 2019
Estimated completion27 February 2020
Sites1 location across Belgium

Drugs / interventions tested

Conditions studied

Sponsor

University of Liege

Who can join

Adults 18 to 65, any sex, with Schizophrenia or Schizo Affective Disorder. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study aims to investigate the effects of the Switch intervention on motivation and associated processes and explore the dynamics between the processes. A single case approach is followed, with a pre-post and follow-up assessment design, and continuous ambulatory assessments (experience sampling method (ESM) and step count).

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Idiographic analyses of motivation and related processes in participants with schizophrenia following a therapeutic intervention for negative symptoms.
    Thonon B, Van Aubel E, Lafit G, Della Libera C, et al · · 2020 · cited 5× · PMID 32977798 · DOI 10.1186/s12888-020-02824-5

Verify or expand the search:

Other recruiting trials for Schizophrenia

Currently open trials in the same condition.

Other University of Liege trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04325100.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing