Communication preferences in glioblastoma

  • Research type

    Research Study

  • Full title

    Communication preferences for glioblastoma treatment: what matters most in times of Covid-19

  • IRAS ID

    292198

  • Contact name

    Florien Boele

  • Contact email

    f.boele@leeds.ac.uk

  • Sponsor organisation

    University of Leeds

  • Duration of Study in the UK

    0 years, 11 months, 31 days

  • Research summary

    Rationale: Patients diagnosed with glioblastoma face a poor prognosis and disease recurrence is inevitable. Treatment is aggressive and includes surgery, radiotherapy and/ or chemotherapy, with a view to balancing benefits for quantity and quality of life. Yet, little is known about how treatment options are communicated to glioblastoma patients and their families, or how this is impacted by the Covid-19 outbreak.

    Objective: We aim to investigate communication preferences of the context of glioblastoma. Outcomes will be used to develop communication guidelines for clinicians so that glioblastoma patients and their families can have more helpful, informed, and patient-centred discussions regarding treatment options.

    Study design: Qualitative study with semi-structured interviews.

    Study population: Adult (≥18 years of age) patients diagnosed with a histologically confirmed glioblastoma, their family carers, and healthcare professionals involved in the care of glioblastoma patients.

    Intervention: Not applicable.

    Main study parameters/endpoints: Topics covered in interviews will include experiences of communication around treatment, which treatment benefits matter most, and how communication around treatment has been affected by the Covid-19 outbreak.

    Nature and extent of the burden and risks associated with participation, benefit and group relatedness: There are no direct benefits for participants in this study, but their participation will contribute to better knowledge on communication around treatment. There are small potential risks: patients and carers are confronted with issues that brain tumour patients have, which may pose a psychological burden on them. Moreover, it will cost participants time to complete study procedures, although this is not substantial.

  • REC name

    East Midlands - Nottingham 1 Research Ethics Committee

  • REC reference

    21/EM/0006

  • Date of REC Opinion

    21 Jan 2021

  • REC opinion

    Favourable Opinion