Feasibility trial of the HOME intervention.

  • Research type

    Research Study

  • Full title

    Assessing the feasibility and acceptability of a training and support intervention for homelessness hostel staff supporting older residents with memory problems: Work package 3 of HOME (Homeless, Older and experiencing MEmory problems) study.

  • IRAS ID

    324735

  • Contact name

    Penny Rapaport

  • Contact email

    p.rapaport@ucl.ac.uk

  • Sponsor organisation

    University College London

  • ISRCTN Number

    ISRCTN28374317

  • Clinicaltrials.gov Identifier

    UCL Data Protection Registration , Z6364106/2023/02/35

  • Duration of Study in the UK

    2 years, 0 months, 1 days

  • Research summary

    In this study we aim to test the feasibility and acceptability of a co-produced staff focused intervention to support older people with memory problems living in hostel accommodation. We aim to do this in two phases; a pre-pilot study (Phase one) followed by a non-randomised multi-site feasibility trial (Phase two).

    In phase one we will conduct a single pilot of the co-produced six-session HOME intervention in one hostel over three months followed by a three month ‘implementation period’. We will hold a focus group at the end of the three month HOME intervention and conduct a brief semi-structured interview with participating staff at 6 months. The intervention will be refined based on findings from the pilot.

    In phase two we will conduct a non-randomised feasibility trial of the six-session HOME intervention followed by a three month implementation period to see if the intervention is feasible (if hostel staff and residents agree to take part and if we can collect necessary information) and acceptable (if people completed and liked the intervention). We will inform feasibility and test procedures by collecting clinical and cost-effectiveness measures planned for a full trial at baseline and at six-months from participating hostel staff and residents. We will keep records of eligible referrals, consent, intervention attendance and losses to follow-up to inform intervention adherence and acceptability of measures. We will complete qualitative interviews, with 8-10 hostel workers who received the intervention and their managers using a semi-structured interview guide and we will audio record intervention sessions to assess facilitator fidelity to the intervention. We will collect information about how the intervention was delivered, how it was received and what people feel should be changed and how, if it proves useful, it could be rolled out. We will work with patient and public involvement representatives throughout the research process.

  • REC name

    London - Camden & Kings Cross Research Ethics Committee

  • REC reference

    23/LO/0455

  • Date of REC Opinion

    14 Jun 2023

  • REC opinion

    Further Information Favourable Opinion