IN DIALOGUES: Inner dialogues in patients with eating disorders

  • Research type

    Research Study

  • Full title

    IN DIALOGUES: A study to investigate the experience of internal dialogues in patients with eating disorders.

  • IRAS ID

    229004

  • Contact name

    Viviana Aya

  • Contact email

    viviana.aya@kcl.ac.uk

  • Sponsor organisation

    King´s College London

  • Duration of Study in the UK

    2 years, 0 months, 31 days

  • Research summary

    Background: The experience of internal dialogues are commonly experienced by patients with eating disorders (ED). Even though it is a well-established phenomenon reported by patients and clinicians, only a few studies have been conducted in this area. The need for future research is emphasised.

    Aim: Investigate the experience of internal dialogues in patients with eating disorders.

    Participants: A total of 180 participants (N=180) will be recruited in total (i.e. 120 patients, 30 carers and 30 professionals).

    Location and duration: The study will take place in England. Recruitment will last 2 years followed by data analysis and writing up of results. This study along with another study will be part of a part-time PhD programme.

    Participants recruitment: Participants will be recruited from a) Internal research unit database (i.e. participants from this internal database have provided consent to be contacted for other other studies) b) the placement of the study flyer in several public areas, websites and social media (e.g. Twitter and Facebook) c) eating disorder charities and support groups d) academic and public conferences/events e) Consent for contact (C4C) f) interested individuals can contact the researchers by phone, email/post if they would like to take part in the study g) researchers can contact individuals who express their interest in taking part in the study.

    Plan of investigation: Mixed method design to collect and analyse qualitative and quantitative data. Specifically, quantitative data (Study 1) will be collected through questionnaires (completed by patients) and surveys (completed by carers and professionals). Qualitative data from patients, carers and professionals will be collected through online focus groups (Study 2).

  • REC name

    London - Surrey Research Ethics Committee

  • REC reference

    17/LO/1720

  • Date of REC Opinion

    17 Oct 2017

  • REC opinion

    Unfavourable Opinion