Transdiagnostic intervention for Negative Symptoms

  • Research type

    Research Study

  • Full title

    Exploring the effect of a novel psychological intervention for negative symptoms based on transdiagnostic mechanisms of change.

  • IRAS ID

    340016

  • Contact name

    Hamish McLeod

  • Contact email

    Hamish.McLeod@glasgow.ac.uk

  • Sponsor organisation

    University of Glasgow

  • Duration of Study in the UK

    1 years, 0 months, 1 days

  • Research summary

    Psychological therapy options for the negative symptoms of schizophrenia are currently of limited effectiveness. This means that many people with a diagnosis of schizophrenia have ongoing difficulties with motivation, emotional expression, and social functioning. Existing psychological treatment packages include elements that may be redundant or ineffective for these patients. Taking a targeted approach that focuses on specific maintenance processes and mechanisms may be both more effective and more efficient than the “one size fits all” approach that is commonly applied. Providing a tailored treatment package that matches intervention modules to the specific maintenance processes relevant to each person has the potential to produce better therapeutic results more efficiently. Because there currently no flexible and mechanistically targeted intervention for negative symptoms we aim to test out a new flexible treatment package using a single case experimental design approach.

    The main outcome for this study will be change in negative symptoms as measured by clinician administered interview. Secondary outcomes will include data on treatment acceptability, self-reported changes in self confidence, and wearable sensor-based measures of activity levels.

    We aim to recruit people experiencing problematic negative symptoms from in-patient mental health rehabilitation wards across Glasgow. Eligible patients will be provided with the information needed to make an informed decision about participating.

    Those who consent will receive an intervention package tailored to their needs that will last for a planned maximum period of 24 weeks. Participant data will be obtained from questionnaires, interviews, wearable sensors that measure activity levels. The data will be analysed to determine if the intervention is acceptable and to explore signs of effectiveness.

  • REC name

    South West - Cornwall & Plymouth Research Ethics Committee

  • REC reference

    24/SW/0084

  • Date of REC Opinion

    7 Aug 2024

  • REC opinion

    Further Information Favourable Opinion