APOLLO: Personalized rehAbilitation PrOgram in aLLOgeneic Bone Marrow Transplantation

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-70
SponsorUniversity of Alberta

About this trial

People who undergo allogeneic bone marrow transplant for blood cancers receive the highest chemotherapy doses possible that humans can receive and still survive. As a result, they have devastating side effects during the procedure and for many years afterwards. Damage to organs and muscles cause long-lasting physical weakness and the psychological experience is severe enough to be termed 'post traumatic stress disorder' that also lasts for many years. These effects are worsened by the fact that most Canadians live several hours away from treatment and transplant centers, leaving them entirely on their own to manage these difficult long term effects. The APOLLO team will perform a qualitative study to learn the experiences of people undergoing allogeneic bone marrow transplant while they receive access to a supportive care computer 'app' and telephone support from nursing, exercise and nutrition experts. In this way, the APOLLO team will learn the most helpful type and timing of supportive care from those who know best.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

eligible for allogeneic transplantation

Disqualifiers

none

Trial population

individuals scheduled to undergo allogeneic transplantation

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Supportive nursing, nutritional and physical activity with a handheld 'app'

    Behavioral

    Supportive nursing, nutritional and physical activity with a handheld 'app'

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Title: Acceptability of a multimodal supportive care

Description: Questionnaire to assess usefulness of a multimodal supportive care App that includes care navigation (nursing, exercise, nutrition)

Time frame
1 year

Secondary outcomes

Other outcomes

Sponsors and contacts

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