Communication for Early Mobilisation of People Living With Dementia Following Surgery for Hip Fracture

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity of Nottingham

About this trial

This goal of this study is to identify ways that healthcare professionals communicate that are effective in helping a person living with dementia to stand or walk after surgery for a broken hip (hip fracture). We aim to identify 'what works' in successfully helping people with dementia to mobilise early, and share this in practice. The main question the research aims to answer is:

What healthcare professional communication practices are effective in achieving early and continued mobilisation among people living with dementia following hip fracture surgery?

We will use a research method called 'Conversation Analysis', to look at the fine detail of the language healthcare professionals use and responses to it. We will make video recordings of real-life ward care, when healthcare staff are trying to help a person with dementia get up early after hip fracture surgery. We will involve people with dementia in decisions to take part and get agreement from their families before we record anything. We have done this successfully in two previous studies. We will record up to 50 episodes of care on three trauma orthopaedic wards. We will identify specific, practical recommendations and 'teachable' approaches: ways of speaking, or sequences of requests or instructions. We will work with people with dementia, family carers, educators and clinicians to do this. We will use clips of videos in future communication training.

Eligibility criteria

Qualifiers

have a documented diagnosis of dementia

be either waiting for hip fracture surgery or have had hip fracture surgery within the previous 7 days

have someone who can act as their personal consultee, in case they are assessed as lacking capacity during the study.

be registered, student or assistant healthcare practitioners

Disqualifiers

Patients will be excluded if we are unable to gain informed consent or consultee agreement, or if they are expected to die within 7 days.

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

No trial groups listed

Locations

This trial has no locations

Sponsors and collaborators