The development of the PERSONAL-AGILITY intervention
Research type
Research Study
Full title
The development of a tailored 24-hour health behaviour programme for people living with frailty and multiple long-term conditions and their carers (PERSONAL-AGILITY)
IRAS ID
332668
Contact name
Hannah Young
Contact email
Sponsor organisation
University Hospitals of Leicester NHS Trust
Clinicaltrials.gov Identifier
160728 , Edge ID
Duration of Study in the UK
1 years, 4 months, 30 days
Research summary
What is this research about?
The number of people living with two or more long-term conditions (multiple long-term conditions, MLTCs) is increasing. Within this group, some people are also vulnerable to sudden changes in health. They find it difficult to ‘bounce back’ from illness (known medically as ‘frailty’), reducing their ability to live an independent life. Being physically active helps maintain independence, but existing physical activity programmes usually focus on one disease. Only half of vulnerable people with multiple long-term conditions can stick to these, and 9 in 10 cannot achieve physical activity recommendations.
A flexible approach which:
• uses all the ways we move in 24-hours to help people be active even if their health and symptoms are variable
• involves carers, so they may also improve their health
• uses existing support from community groups
may be more acceptable. This study aims to develop this type of programmeWho can participate?
We will include:
- people living with frailty and MLTCs
- health care professionals
- informal carers of people living with frailty and MLTCsWhat is involved?
This study involves two phases.
In the first phase we will ask participants (carers and healthcare professionals) to take part in a one-off group or individual interview to understand their experiences and, needs in relation to 24-hour health behaviours. The results will be added to research we have already completed with people living with frailty and MLTCs, and inform the content and design of the programme.
The second phase will start once we have created a prototype intervention. We will ask participants (people with MLTCs and frailty, carers and healthcare professionals) to take part in a ‘think aloud’ interview to find out what they think about the prototype whilst they are using it. The results will be used to improve the programme.REC name
South Central - Oxford B Research Ethics Committee
REC reference
23/SC/0402
Date of REC Opinion
27 Nov 2023
REC opinion
Further Information Favourable Opinion