Early Psychosis: Investigating Cognition (EPIC)

  • Research type

    Research Study

  • Full title

    Glutamate changes as a new neurocognitive marker in psychosis

  • IRAS ID

    346223

  • Contact name

    Claudia Danielmeier

  • Contact email

    claudia.danielmeier@nottingham.ac.uk

  • Sponsor organisation

    University of Nottingham

  • Clinicaltrials.gov Identifier

    NCT00000000

  • Duration of Study in the UK

    1 years, 2 months, 31 days

  • Research summary

    Cognitive impairments occur in up to 80% of people with psychosis. Current interventions are effective for some, but not all, individuals with psychosis. To increase the amount of viable and effective treatment options, a personalised approach based on improved understanding into the variability in cognitive impairments in psychosis is needed. This Wellcome Trust funded project aims to explore perceptions of cognitive impairment and treatment from those with first-hand experience (Study 2); to explore a potential neurochemical marker (glutamate levels, in particular) for cognitive functioning with a focus on working memory (Study 1a); and to assess how this marker may predict changes in response to a single 'accelerated’ session of non-invasive brain stimulation using transcranial direct current stimulation (tDCS) (study 1a). Additionally, the study aims to explore the effects of accelerated tDCS on neurochemistry in individuals with first episode psychosis (FEP) (Study 1b). Through these three interconnected studies using functional magnetic resonance spectroscopy, tDCS and interview approaches, we aim to better understand and inform potential future treatment options for cognitive impairment in psychosis.

    The data collection phase of the study will last approximately 12-30 months. An additional year will be spent on analysis and write up. In total, a participant’s involvement will take up to 3 months for Study 1 and 1 month for Study 2, including initial contact and recruitment.

    FEP participants will typically take part in 1-5 sessions across studies. Study 1a involves the completion of two sessions which should be approximately 1-7 days apart and a 2-month follow-up. Participants also taking part in study 1b will do so on the same day as part 2 of study 1a. Study 2 may be completed before or after studies 1a and 1b or independently of them. Control participants will only be invited to take part in some aspects of 1a.

  • REC name

    London - Stanmore Research Ethics Committee

  • REC reference

    25/LO/0427

  • Date of REC Opinion

    18 Aug 2025

  • REC opinion

    Further Information Favourable Opinion