A phase 2 study of a longitudinal multidimensional rehabilitation program for allogeneic blood and marrow transplantation patients

Author:

Tam Samantha12ORCID,Alibhai Shabbir M. H.34,Hassanieh Dima2,Kumar Rajat5ORCID,Mattsson Jonas5,Atenafu Eshetu G.6ORCID,Avery Lisa6ORCID,Bernstein Lori J.27ORCID,Chang Eugene2,Langelier David2ORCID,Lopez Paty2,Jones Jennifer M.12

Affiliation:

1. 1Institute of Medical Science, University of Toronto, Toronto, ON, Canada

2. 2Department of Supportive Care, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada

3. 3Department of Medicine, University Health Network, Toronto, ON, Canada

4. 4Department of Medicine, University of Toronto, Toronto, ON, Canada

5. 5Hans Messner Allogeneic Transplant Program, Princess Margaret Cancer Centre, University Health Network, University of Toronto, Toronto, ON, Canada

6. 6Department of Biostatistics, Princess Margaret Cancer Centre, University of Toronto, Toronto, ON, Canada

7. 7Department of Psychiatry, University of Toronto, Toronto, ON, Canada

Abstract

Abstract Allogeneic blood and marrow transplantation (alloBMT) is a curative treatment for blood cancers associated with various treatment-related adverse events and morbidities for which rehabilitation programs are currently limited. A phase 2 randomized controlled trial (RCT) was conducted to assess the feasibility, acceptability, and impact of CaRE-4-alloBMT, a longitudinal, multidimensional cancer rehabilitation program for patients undergoing alloBMT. The primary outcomes included the feasibility and acceptability of the intervention and the methods. Feasibility was assessed through recruitment, retention, and adherence rates. Acceptability was assessed through qualitative interviews. Secondary clinical outcomes were collected through questionnaires and physiological assessments at 4 time points. A total of 80 participants were recruited and randomized. Recruitment (72%) and retention (70%) rates, along with qualitative findings, support the feasibility of the intervention. Adherence was suboptimal, most notably educational module completion (22.7%). Treatment effect sizes of 0.70 (95% confidence interval [CI], 0.20-1.21; 30-second sit-to-stand test) and 0.46 (95% CI, –0.17 to 1.09; 36-Item Short Form Survey) were observed in favor of the intervention. The results appear promising; however, the findings are limited by missing data owing to attrition. Modifications will be required to refine the program and inform a phase 3 RCT. This trial was registered at www.ClinicalTrials.gov as #NCT04966156.

Publisher

American Society of Hematology

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