The CADENCE pilot trial - Promoting physical activity in bladder cancer survivors: A protocol paper.

Bladder cancer Cancer survivor Co-design intervention Home-based exercise

Journal

Contemporary clinical trials communications
ISSN: 2451-8654
Titre abrégé: Contemp Clin Trials Commun
Pays: Netherlands
ID NLM: 101671157

Informations de publication

Date de publication:
Jun 2021
Historique:
received: 21 01 2021
revised: 01 06 2021
accepted: 13 06 2021
entrez: 1 7 2021
pubmed: 2 7 2021
medline: 2 7 2021
Statut: epublish

Résumé

Participation in physical activity has been found to be beneficial for mental and physical health outcomes among cancer survivors. However, to date no intervention exists specifically to promote physical activity among bladder cancer survivors. In light of this knowledge a home-based exercise intervention was co-created for those recently diagnosed with bladder cancer. The aim of the present study, financially supported by Action Bladder Cancer UK [1], is to pilot the home-based exercise intervention tailored specifically for bladder cancer survivors (i.e. from the point of diagnosis) to improve physical and mental health outcomes (during treatment and beyond) in this population. This study will use a randomised controlled trial design. Arm one will consists of the 14 week home-based exercise intervention and arm two usual care (15 participants will be randomised to each arm). Baseline data collection will take place shortly after clinical diagnosis of bladder cancer, and follow-up approximately 7 weeks and then again approximately 14 weeks after commencement of the intervention. At each data collection point data will be collected from participants relating to demographics, physical and mental health. Participants will aslo be asked to wear an Actigraph Accelerometer at each data collection point for seven consecutive days. Immediately after baseline data collection participants in the intervention arm will be given the home-based exercise booklet. Ethical approval was obtained for the present study via The London- City and East Research Ethics Committee (ID:291676). Results of this study will be disseminated through peer-reviewed publications and scientific presentations.

Sections du résumé

BACKGROUND BACKGROUND
Participation in physical activity has been found to be beneficial for mental and physical health outcomes among cancer survivors. However, to date no intervention exists specifically to promote physical activity among bladder cancer survivors. In light of this knowledge a home-based exercise intervention was co-created for those recently diagnosed with bladder cancer.
AIM OBJECTIVE
The aim of the present study, financially supported by Action Bladder Cancer UK [1], is to pilot the home-based exercise intervention tailored specifically for bladder cancer survivors (i.e. from the point of diagnosis) to improve physical and mental health outcomes (during treatment and beyond) in this population.
METHODS METHODS
This study will use a randomised controlled trial design. Arm one will consists of the 14 week home-based exercise intervention and arm two usual care (15 participants will be randomised to each arm). Baseline data collection will take place shortly after clinical diagnosis of bladder cancer, and follow-up approximately 7 weeks and then again approximately 14 weeks after commencement of the intervention. At each data collection point data will be collected from participants relating to demographics, physical and mental health. Participants will aslo be asked to wear an Actigraph Accelerometer at each data collection point for seven consecutive days. Immediately after baseline data collection participants in the intervention arm will be given the home-based exercise booklet.
ETHICS AND DISSEMINATION BACKGROUND
Ethical approval was obtained for the present study via The London- City and East Research Ethics Committee (ID:291676). Results of this study will be disseminated through peer-reviewed publications and scientific presentations.

Identifiants

pubmed: 34195472
doi: 10.1016/j.conctc.2021.100809
pii: S2451-8654(21)00110-1
pmc: PMC8239430
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100809

Informations de copyright

© 2021 The Authors.

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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Auteurs

Lee Smith (L)

The Cambridge Centre for Sport and Exercise Sciences, Anglia Ruskin University, Cambridge, CB1 1PT, UK.

Anne Carrie (A)

The Queen Elizabeth Hospital Foundation Trust, King's Lynn, UK.

Mark Tully (M)

Institute of Mental Health Sciences, School of Health Sciences, Ulster University, Newtownabbey, BT37 0QB, UK.

Yvonne Barnett (Y)

Faculty of Science and Technology, Anglia Ruskin University, Cambridge, CB1 1PT, UK.

Laurie Butler (L)

Faculty of Science and Technology, Anglia Ruskin University, Cambridge, CB1 1PT, UK.

Claire Gillvray (C)

Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.

Rosie Lindsay (R)

Vision and Hearing Sciences Research Center, Anglia Ruskin University, Cambridge, CB1 1PT, UK.

Adam Abbs (A)

Pennine Acute Hospitals, NHS Trust, UK.

Mike Trott (M)

The Cambridge Centre for Sport and Exercise Sciences, Anglia Ruskin University, Cambridge, CB1 1PT, UK.

Olawale Olanrewaju (O)

The Cambridge Centre for Sport and Exercise Sciences, Anglia Ruskin University, Cambridge, CB1 1PT, UK.
The Queen Elizabeth Hospital Foundation Trust, King's Lynn, UK.

Lin Yang (L)

Department of Cancer Epidemiology and Prevention, Cancer Care Alberta, Alberta Health Services,Calgary, AB T2S 3C3, Canada.

Cristian Petre Ilie (CP)

The Queen Elizabeth Hospital Foundation Trust, King's Lynn, UK.

Classifications MeSH