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Investigating the impact of multidisciplinary prehabilitation on deconditioning in patients eligible for haematopoietic allogenic stem cell transplantation: protocol for a feasibility trial
  1. Karlee Naumann1,
  2. Ben Singh2,
  3. Samuel Bushaway1,
  4. Rhiannon Crane1,
  5. Swapna Deepak1,
  6. Amie Hartland1,
  7. Peter Konstantopoulos1,
  8. Ella Mansell1,
  9. Vanessa Marinelli1,
  10. Vanessa Pallotta1,
  11. Annabel Tolfts1,
  12. Alison Virieux1,
  13. Michelle Wall1,
  14. Sarah Wilksch1,
  15. Mabel Zhuang1,
  16. Morgan Atkinson1,
  17. Carol Maher2
  1. 1Royal Adelaide Hospital, Adelaide, South Australia, Australia
  2. 2University of South Australia, Adelaide, South Australia, Australia
  1. Correspondence to Dr Ben Singh; ben.singh{at}unisa.edu.au

Abstract

Background Assessing multidisciplinary prehabilitation strategies becomes crucial to pre-emptively counter the physical, psychological and social negative impacts experienced during an allogenic haematopoietic stem cell transplant (allo-HSCT) among acute myeloid leukaemia (AML) and myelodysplastic syndrome (MDS) patients. Current evidence is restricted to studies during induction chemotherapy, omitting rehabilitation interventions and predominantly using exercise-only approaches without a multidisciplinary framework. The aim of this study is to investigate the feasibility, safety and preliminary efficacy of multidisciplinary prehabilitation in adults offered allo-HSCT.

Methods and analysis This 8-week single-group pre-post feasibility study aims to pilot a multidisciplinary prehabilitation intervention for participants undergoing allo-HSCT, with a focus on feasibility and safety. Participants, aged 18 or older, diagnosed with AML or MDS, and offered allo-HSCT, will be recruited between June 2023 and July 2024. The multidisciplinary prehabilitation intervention, conducted by the cancer allied health team at the Royal Adelaide Hospital, includes exercise physiology, physiotherapy, dietetics, social work, occupational therapy and psychology interventions. Consistent with a multidisciplinary treatment approach, each component is tailored to address different aspects of patient care, and adherence calculations will assess patient engagement and compliance. In addition, participants will continue to receive usual care from cancer allied health staff. The primary outcome of the study is to assess the feasibility of a multidisciplinary prehabilitation intervention by evaluating intervention uptake, retention, adherence, acceptability and safety. Secondary outcomes are leg strength, upper-body strength, aerobic fitness, falls risk, anthropometry, nutritional status, quality of life, anxiety, depression, self-efficacy for coping with cancer and distress.

Ethics and dissemination Ethics approval for this study has been provided by the Central Adelaide Local Health Network (HREC 2022/HRE00284). Recruitment for the study commenced in June 2023 and will continue until July 2024. The methods have been designed and are reported according to the SPIRIT and CONSORT-pilot study checklist.

Trial registration number The Australian New Zealand Clinical Trials Registry (ANZCTR): ACTRN12623000052639.

  • Bone marrow transplantation
  • HAEMATOLOGY
  • PREVENTIVE MEDICINE

Data availability statement

No data are available. This is a protocol and no data has been collected yet.

http://creativecommons.org/licenses/by-nc/4.0/

This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.

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Data availability statement

No data are available. This is a protocol and no data has been collected yet.

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Footnotes

  • X @bensinghphd

  • Contributors Study concept was conceived by MA, KN and CM. Study design was devised by all authors. KN, SB, RC, SD, AH, PK, VM, EM, VP, AT, AV, MW, SW, MZ and MA are involved in recruitment, intervention delivery and data collection. KN and BS wrote the first draft of the protocol, and all authors contributed to some part. BS is the guarantor. All authors have read and approved the final manuscript.

  • Funding CM is supported by a Medical Research Future Fund Emerging Leader Grant (GNT1193862).

  • Competing interests None declared.

  • Patient and public involvement Patients and/or the public were not involved in the design, or conduct, or reporting, or dissemination plans of this research.

  • Provenance and peer review Not commissioned; externally peer reviewed.