SHAPE

  • Research type

    Research Study

  • Full title

    Self-management and HeAlth Promotion in early-stage dementia with E-learning for carers – SHAPE. A multicentre, randomised, controlled trial.

  • IRAS ID

    258388

  • Contact name

    Ingelin Testad

  • Contact email

    i.testad@exeter.ac.uk

  • Sponsor organisation

    Stavanger University Hospital

  • Clinicaltrials.gov Identifier

    NCT04286139

  • Duration of Study in the UK

    1 years, 5 months, 31 days

  • Research summary

    Will an educational programme combining approaches of self-management, health promotion, and e-learning, improve self-efficacy and other key health and mental health outcomes for people with mild to moderate dementia?

    It is currently estimated that 47 million people are living with dementia today and this number is expected to double in the next 20 years. Unfortunately, there has been limited advancement in medical treatments for dementia and new cost-effective approaches are needed. The utility of self-management has been proven to be of benefit in certain chronic diseases, however, very little work has been undertaken regarding self-management in people with dementia.

    The SHAPE self-management group therapy aims to significantly improve self–efficacy in people with mild to moderate dementia and to improve key health and mental health outcomes, carer stress and knowledge of dementia. SHAPE comprises a 10 week course delivered as group sessions for the participants with dementia. The sessions are designed to develop self-management skills and to provide information on the disease process and the development of healthy behaviours in a supportive learning environment to prevent problems that are common in the later stages of the disease. E-learning resources will be provided for carers (study supporters) which covers the similar and complimentary material discussed in the group sessions for the participant with dementia.

    This trial uses 2:1 randomisation and will assess the clinical and cost effectiveness of SHAPE. Participants will be randomised to participate in the SHAPE intervention or continue with usual care. To assess the effectiveness of SHAPE at improving self-efficacy and secondary outcomes a battery of questionnaires will be administered to the participants and study supporters at baseline, 3 months after randomisation; after SHAPE participants have completed the intervention, and 9 months after randomisation. The answers to these questionnaires will be assessed and the results compared between the two groups of participants.

  • REC name

    South West - Frenchay Research Ethics Committee

  • REC reference

    19/SW/0210

  • Date of REC Opinion

    9 Mar 2020

  • REC opinion

    Further Information Favourable Opinion