Bipolar disorder, interoception and emotion recognition

  • Research type

    Research Study

  • Full title

    Exploring bipolar disorder and its relationships with interoception and emotion recognition (Worktribe Reference: 420322)

  • IRAS ID

    298130

  • Contact name

    Nadzeya Svirydzenka

  • Contact email

    nadzeya.svirydzenka@dmu.ac.uk

  • Sponsor organisation

    De Montfort University

  • Clinicaltrials.gov Identifier

    420322, DMU Worktribe

  • Duration of Study in the UK

    0 years, 10 months, 2 days

  • Research summary

    This study aims to investigate emotional experience in bipolar disorder (BD) from a physiological and cognitive perspective with the former being of particular relevance. The physiological perspective proposes emotions are generated from organs such as the heart where research has shown different rhythms associated with different emotions. The cognitive processing of emotions will also be investigated in this study to support the existing evidence of emotional processing differences using a facial emotion recognition (FER) task whilst accounting for a range of important variables.

    The physiological perspective of emotion has not been looked at objectively before in BD despite there being overwhelming evidence to support differences in this function in depression. To assess physiological functioning, it is possible to assess signals internally using interoception. Interoception is a construct concerned with the ability to perceive signals from within the body. The heartbeat counting task is a frequently used measure of interoception that assesses the ability to feel heartbeats. For participants that exhibit poor perception of signals from within, studies have suggested there is a blunted emotional experience. The blunting of emotional experiences impacts social functioning and interpersonal relationships negatively and this can have a profound impact on recovery in mental health and daily functioning.

    This study aims to recruit a sample with bipolar disorder to identify if differences exist in the experience of emotions from both perspectives similar to results in depression. An at-risk sample is used to highlight potential developmental markers of emotional processing differences and a comparison control sample. Participants will complete validated self-report questionnaires and FER, self-assessment manikin, and heartbeat counting tasks. A questionnaire will be sent to the clinical participant’s healthcare team to collect data relating to their BD diagnosis. A pilot study suggests the time of completion for the experiment is between 60-75 minutes.

  • REC name

    North of Scotland Research Ethics Committee 2

  • REC reference

    22/NS/0132

  • Date of REC Opinion

    23 Dec 2022

  • REC opinion

    Further Information Favourable Opinion