Prehabilitation Closer to Home Study: Novel Evaluation of a Co-designed Pre-habilitation Exercise service for Haematological Cancer Patients Preparing for Bone Marrow Transplantation.
- Conditions
- Haematological CancerCancer - Hodgkin'sCancer - Leukaemia - Acute leukaemiaCancer - Leukaemia - Chronic leukaemiaCancer - Lymphoma (non Hodgkin's lymphoma) - High grade lymphomaCancer - Lymphoma (non Hodgkin's lymphoma) - Low grade lymphomaCancer - Myeloma
- Registration Number
- ACTRN12624000363583
- Lead Sponsor
- The University of Melbourne
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 60
Patient Inclusion Criteria
•Aged 18 years or older
•Awaiting a bone marrow transplant
•Diagnosis of a haematological malignancy
•Able to ambulate independently
•Willing to complete baseline and pre-transplant study related assessments
•Proficient in English to understand exercise testing and training instructions as well as to complete study consent form and questionnaires – or have someone who can assist with this.
Staff Inclusion Criteria (qualitative study only)
•Aged 18 years or older
•Proficient in English to complete study consent form and interview – or have someone who can assist with this.
•Involved in delivery or management of the exercise prehabilitation service for patients with a haematological malignancy during the trial period.
Patient Exclusion Criteria
•More than one active malignancy, or receiving BMT for non-haematological disease
•Severe or unstable neurological, cardiorespiratory or musculoskeletal disease or mental illness that might compromise ability to perform exercise
•Less than 2 weeks between recruitment and scheduled admission for transplant.
Staff Exclusion criteria (qualitative study only)
•Is a named investigator on the trial. Investigators involved in service delicery can provide feedback during the co-design meeting but will not be invited to participate in the qualitative interviews.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method