PASE ABI study v1.5

  • Research type

    Research Study

  • Full title

    Physical Activity, Fatigue and Self-Efficacy in Children with Acquired Brain Injury, Brain Tumours and Neurological Conditions: A Questionnaire Study

  • IRAS ID

    255778

  • Contact name

    Sophie Thomas

  • Contact email

    sophie.thomas@nhs.net

  • Sponsor organisation

    Nottingham University Hospitals

  • Duration of Study in the UK

    1 years, 5 months, 1 days

  • Research summary

    Acronyms:
    ABI - Acquired brain injury
    CYP - Children and young person
    PA - Physical activity

    BACKGROUND
    Growing evidence has shown that PA can be beneficial for emotional, physical and cognitive recovery. Furthermore, it has been shown that exercise can contribute to an improvement in mood and quality of life in adults with brain injury. Through our clinical observations, CYP with ABI are physically inactive relative to their peers. Many lack structured daily activity, and suffer fatigue, poor sleep, low self esteem and social isolation. Research has demonstrated that PA can have positive outcomes on health and psychological wellbeing of CYP with long-term conditions such as cerebral palsy. However, to our knowledge, there are no published studies of PA levels in CYP and other forms of brain injury or neurological conditions.

    AIM
    1) To increase the understanding of PA levels for young people with ABI, brain tumours and neurological conditions
    2) To explore if the following variables can predict PA: socioeconomic status, parental PA levels, physical illness symptoms, fatigue, disability and health related anxiety regarding exercise

    This will allow us to understand those most likely to become underactive following acquired brain injury in childhood and inform the targeting of interventions to support physical activity in this population.

    Finally, we also aim to ask participants and parents their views on CYP taking part in an intervention to increase their PA levels to inform plans for a future intervention study.

    SETTING
    The study will involve 2 NHS hospitals in England.

    METHODS
    Data will be collected by questionnaires administered to participants at the 2 hospitals in England during their outpatient clinic visits. Permission and support from the medical consultants running these clinics has already been established.

  • REC name

    London - Bromley Research Ethics Committee

  • REC reference

    19/LO/1324

  • Date of REC Opinion

    19 Aug 2019

  • REC opinion

    Further Information Favourable Opinion