Fact CheckerSign in

NCT05703698Completed

EEG Outcomes From Cognitive Behavioural Therapy for Psychosis

Source: ClinicalTrials.gov · Last updated 29 Jul 2025

Brief summary (registry, in English)

Despite overwhelming evidence for neurocognitive and neurophysiological factors involved in the etiology of psychosis, these factors have never been examined as mechanisms of improvement from CBTp. The first aim in the present study is to examine neurophysiological outcomes from CBTp using electroencephalography (EEG). The second aim is to examine neurocognitive outcomes from CBTp. This is an open-label pilot study. Twenty participants will receive CBTp and will be assessed at baseline and after 4 months.

Status (registry)
Completed
Study type
Interventional
Enrollment
20 (actual)
First submitted
19 Jan 2023
Start date
1 Feb 2023
Primary completion date
13 Nov 2024
Lead sponsor
University of Toronto
NCT number
NCT05703698

What you commit to

  • Study type: Interventional
  • Participants enrolled: 20
  • From 1 Feb 2023 to the primary completion date, 13 Nov 2024
  • 1 site 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.

Other illness

  • Exclusion criteria include anyone with a neurological disease or neurological damage, medical illnesses that can change neurocognitive function, a medical history of head injury with loss of consciousness and those with physical handicaps that would prevent them from engaging in assessment procedures

Who the study is looking for

  • The inclusion criteria is anyone who meets the criteria of schizophrenia, schizoaffective disorder or any other psychotic disorder, are also 18-65 years of age, are not abusing drugs or alcohol and can read and speak English. Participants must be experiencing active symptoms of psychosis as indicated on the PANSS.

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Toronto Scarborough
Coordinator of this site? Confirm its status
Scarborough VillageCanadaUnknown status

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