Measuring Wellbeing in People with Neurological Conditions

  • Research type

    Research Study

  • Full title

    Exploring a Client-Rated Outcome Measure of Wellbeing During Neurological Rehabilitation

  • IRAS ID

    251235

  • Contact name

    Franziska Leutner

  • Contact email

    f.leutner@ucl.ac.uk

  • Sponsor organisation

    University College London

  • Clinicaltrials.gov Identifier

    UCL Data Protection Registration, Z6364106/2018/08/70

  • Duration of Study in the UK

    0 years, 8 months, 21 days

  • Research summary

    This project aims to develop a questionnaire that can be used to measure the wellbeing of clients who have a neurological condition. People with such conditions often have cognitive, physical and language impairments which make it difficult for them to use many measures of mood and wellbeing. The questions asked are often difficult to answer when you have a neurological condition. For example, measures of mood often ask if people feel slowed down or lacking in energy, both are very common symptoms of neurological conditions and not necessarily a reflection of their mood or wellbeing. Our community neuro-rehabilitation team routinely measures mood (anxiety and depression) through self report (Hospital Anxiety and Depression Scale- HADS) and client wellbeing through a therapist rated scale (TOM).

    We would like to understand our client's wellbeing from their perspective. We would like to be able to accurately monitor their wellbeing at the during their rehabilitation and use this information to inform and improve their treatment.

    All clients attending Islington Community Neurorehabilitation Team (ICNRT) for rehabilitation would be eligible to take part. The study would take place at the ICNRT premises: Islington Outlook. All participants would be required to complete two short questionnaires; the Hospital Anxiety and Depression Scale (HADS) and the newly developed wellbeing scale. Treating therapists would (as is routine clinical practice) complete the Therapy Outcome Measure (TOMs) for each participant. All measures would be completed at the start and end of treatment.

    This study would gather data between November/December 2018 and February/March 2019, based on the earliest the study receives ethical approval. We hope to write up the study to be published in a journal article. If the questionnaire is found to be helpful we would make it available to be used in routine clinical practice.

  • REC name

    Wales REC 6

  • REC reference

    18/WA/0367

  • Date of REC Opinion

    22 Oct 2018

  • REC opinion

    Further Information Favourable Opinion