Evidence map›Paper›PMID 42149831›Full record

ArticlePloS one2026

Maintaining function and participation through tailored 24-hour movement behaviours for people living with multiple long-term conditions and frailty (The PERSONAL-AGILITY study): Protocol for a randomised controlled feasibility trial.

Martha Thomas, Louisa Y Herring, Melanie J Davies, Lucina Wilde, Vicky Hall, Laura J Gray, Sharlene A Greenwood, Michelle Hadjiconstantinou, Malak Hamza, Andrew Harris and 10 more

Abstract readClinical Trial Protocol
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Martha ThomasNIHR Leicester Biomedical Research Centre, University of Leicester and University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.
Louisa Y HerringNIHR Leicester Biomedical Research Centre, University of Leicester and University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.
Melanie J DaviesNIHR Leicester Biomedical Research Centre, University of Leicester and University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.ORCID https://orcid.org/0000-0002-9987-9371
Lucina WildeNIHR Leicester Biomedical Research Centre, University of Leicester and University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.
Vicky HallNIHR Leicester Biomedical Research Centre, University of Leicester and University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.
Laura J GrayDivision of Public Health and Epidemiology, University of Leicester, Leicester, United Kingdom.
Sharlene A GreenwoodDepartment of Renal Medicine, King's College Hospital NHS Trust, London, United Kingdom.
Michelle HadjiconstantinouNIHR Leicester Biomedical Research Centre, University of Leicester and University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.
Malak HamzaNIHR Leicester Biomedical Research Centre, University of Leicester and University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.
Andrew HarrisActive Together, Leicestershire County Council, Glenfield, Leicester, United Kingdom.
Jemma HawkinsCentre for Development, Evaluation, Complexity and Implementation in Public Health Improvement (DECIPHer), School of Social Sciences, Cardiff University, Cardiff, United Kingdom.
Kamlesh KhuntiNIHR Leicester Biomedical Research Centre, University of Leicester and University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.
Matthew MaddocksCicely Saunders Institute of Palliative Care, Policy & Rehabilitation, Kings College London, England.
Atulkumar RajparaNIHR Leicester Biomedical Research Centre, University of Leicester and University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.
Alex RowlandsNIHR Leicester Biomedical Research Centre, University of Leicester and University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.ORCID https://orcid.org/0000-0002-1463-697X
Priscilla SarkarNIHR Leicester Biomedical Research Centre, University of Leicester and University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.
Avan A SayerAGE Research Group, NIHR Newcastle Biomedical Research Centre, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University and Newcastle Upon Tyne Hospitals NHS Foundation Trust, Newcastle-Upon-Tyne, United Kingdom.
Sam SeiduNIHR Leicester Biomedical Research Centre, University of Leicester and University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.ORCID https://orcid.org/0000-0002-8335-7018
Tom YatesNIHR Leicester Biomedical Research Centre, University of Leicester and University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.
Hannah M L YoungNIHR Leicester Biomedical Research Centre, University of Leicester and University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.ORCID https://orcid.org/0000-0002-4249-9060

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMaintaining function and participation through tailored 24-hour movement behaviours for people living with multiple long-term conditions (MLTC) and frailty (The PERSONAL-AGILITY study) is a research programme which aims to develop and evaluate a complex behaviour change intervention. The intervention uses a range of approaches tailored for individuals living with MLTC and frailty, and their carers, incorporating novel technology to improve 24-hour movement behaviours and, consequently, quality of life and physical function. This paper outlines the protocol for a randomised controlled trial (RCT) evaluating the feasibility and acceptability of the PERSONAL-AGILITY intervention, study design and procedures. METHODS AND ANALYSIS: A feasibility RCT, with 2:1 allocation to the PERSONAL-AGILITY intervention or usual care control. The primary outcome is the feasibility and acceptability of a future definitive RCT investigating the effectiveness of the PERSONAL-AGILITY intervention, assessed against prespecified progression criteria, including eligibility, recruitment, retention, and outcome measure completion rates. The trial will be conducted at the University Hospitals of Leicester and comprise a 24-week tailored behaviour change intervention delivered by members of the PERSONAL-AGILITY research team. A target sample of 50 people with MLTC and frailty, and their carer (optional), will be recruited. A range of secondary outcomes including body composition, blood pressure, physical activity, sleep, physical function, and quality of life will be assessed at baseline, 12, and 24 weeks to help identify the primary or co-primary outcomes for participants with MLTC and frailty and their carers. A mixed methods process evaluation will examine the acceptability, feasibility and fidelity of intervention delivery and trial procedures. This study will inform the feasibility and design of a future definitive RCT. ETHICS AND DISSEMINATION: The trial has been approved by South Central Oxford B Research Ethics Committee (Ref: 24/SC/0367). Participants will be asked to provide consent to take part in the PERSONAL-AGILITY study by a trained member of the research team. Findings will be disseminated via peer reviewed journals, presentations and communications with health care professionals, patients and the public. Trial registration: International Standard Randomised Controlled Trial Number 14362764. URL to registry record: https://www.isrctn.com/ISRCTN14362764. Date of registration: 25th November 2024.

Indexed as

ExerciseFrailtyAgedChronic DiseaseFeasibility StudiesFemaleFrail ElderlyHumansMaleQuality of LifeRandomized Controlled Trials as Topic

Identifiers

PMID42149831
PMCPMC13183243

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.