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Study protocol for a pragmatic randomised controlled trial of comparing enhanced acceptance and commitment therapy plus (+) added to usual aftercare versus usual aftercare only, in patients living with or beyond cancer: SUrvivors' Rehabilitation Evaluation after CANcer (SURECAN) trial.
Khan, Imran; Taylor, Stephanie J C; Robinson, Clare; Moschopoulou, Elisavet; McCrone, Paul; Bourke, Liam; Thaha, Mohamed; Bhui, Kamaldeep; Rosario, Derek; Ridge, Damien; Donovan, Sheila; Korszun, Ania; Little, Paul; Morgan, Adrienne; Quentin, Olivier; Roylance, Rebecca; White, Peter; Chalder, Trudie.
Afiliação
  • Khan I; Barts and the London Centre for Primary Care, Wolfson Institute of Population Health, Queen Mary University of London, London, UK. Imran.Khan@qmul.ac.uk.
  • Taylor SJC; Barts and the London Centre for Primary Care, Wolfson Institute of Population Health, Queen Mary University of London, London, UK. s.j.c.taylor@qmul.ac.uk.
  • Robinson C; Barts and the London Pragmatic Clinical Trials Unit, Centre for Evaluation and Methods, Wolfson Institute of Population Health, Queen Mary University of London, London, UK.
  • Moschopoulou E; Barts and the London Centre for Primary Care, Wolfson Institute of Population Health, Queen Mary University of London, London, UK.
  • McCrone P; Institute for Lifecourse Development, University of Greenwich, London, UK.
  • Bourke L; Dept. Allied Health Professionals, Sheffield Hallam University, Sheffield, UK.
  • Thaha M; Blizard Institute, Queen Mary University of London, London, UK.
  • Bhui K; Nuffield Department of Primary Care Health Sciences, Wadham College, University of Oxford, Oxford, UK.
  • Rosario D; The Academic Urology Unit, University of Sheffield, Sheffield, UK.
  • Ridge D; School of Social Sciences, University of Westminster, New Cavendish St, London, UK.
  • Donovan S; Barts and the London Centre for Primary Care, Wolfson Institute of Population Health, Queen Mary University of London, London, UK.
  • Korszun A; The Barts and the London Unit for Psychological Medicine, Centre for Psychiatry and Mental Health, Wolfson Institute of Population Health, Queen Mary University of London, London, UK.
  • Little P; Primary Care Research Centre, Faculty of Medicine, University of Southampton, Southampton, UK.
  • Morgan A; Independent Cancer Patient's Voice (ICPV), 17 Woodbridge Street, London, UK.
  • Quentin O; Barts and the London Pragmatic Clinical Trials Unit, Centre for Evaluation and Methods, Wolfson Institute of Population Health, Queen Mary University of London, London, UK.
  • Roylance R; University College London Hospitals NHS Foundation Trust, London, UK.
  • White P; The Academic Urology Unit, University of Sheffield, Sheffield, UK.
  • Chalder T; Institute of Psychiatry, Psychology & Neuroscience (IoPPN), King's College London, DeCrespigny Park, London, UK.
Trials ; 25(1): 228, 2024 Apr 02.
Article em En | MEDLINE | ID: mdl-38566197
ABSTRACT

BACKGROUND:

Two million people in the UK are living with or beyond cancer and a third of them report poor quality of life (QoL) due to problems such as fatigue, fear of cancer recurrence, and concerns about returning to work. We aimed to develop and evaluate an intervention based on acceptance and commitment therapy (ACT), suited to address the concerns of cancer survivors and in improving their QoL. We also recognise the importance of exercise and vocational activity on QoL and therefore will integrate options for physical activity and return to work/vocational support, thus ACT Plus (+).

METHODS:

We will conduct a multi-centre, pragmatic, theory driven, randomised controlled trial. We will assess whether ACT+ including usual aftercare (intervention) is more effective and cost-effective than usual aftercare alone (control). The primary outcome is QoL of participants living with or beyond cancer measured using the Functional Assessment of Cancer Therapy General scale (FACT-G) at 52 weeks. We will recruit 344 participants identified from secondary care sites who have completed hospital-based treatment for cancer with curative intent, with low QoL (determined by the FACT-G) and randomise with an allocation ratio of 11 to the intervention or control. The intervention (ACT+) will be delivered by NHS Talking Therapies, specialist services, and cancer charities. The intervention consists of up to eight sessions at weekly or fortnightly intervals using different modalities of delivery to suit individual needs, i.e. face-to-face sessions, over the phone or skype.

DISCUSSION:

To date, there have been no robust trials reporting both clinical and cost-effectiveness of an ACT based intervention for people with low QoL after curative cancer treatment in the UK. We will provide high quality evidence of the effectiveness and cost-effectiveness of adding ACT+ to usual aftercare provided by the NHS. If shown to be effective and cost-effective then commissioners, providers and cancer charities will know how to improve QoL in cancer survivors and their families. TRIAL REGISTRATION ISRCTN ISRCTN67900293 . Registered on 09 December 2019. All items from the World Health Organization Trial Registration Data Set for this protocol can be found in Additional file 2 Table S1.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 11_ODS3_cobertura_universal / 1_ASSA2030 / 2_ODS3 Base de dados: MEDLINE Assunto principal: Terapia de Aceitação e Compromisso / Neoplasias Limite: Humans Idioma: En Revista: Trials Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 11_ODS3_cobertura_universal / 1_ASSA2030 / 2_ODS3 Base de dados: MEDLINE Assunto principal: Terapia de Aceitação e Compromisso / Neoplasias Limite: Humans Idioma: En Revista: Trials Ano de publicação: 2024 Tipo de documento: Article