ACTRN12620000271909
Not yet recruiting
未知
Geriatric assessment of frailty in patients with Haematological Malignancies - A study determining the impact of frailty in older people with haematological malignancies.
Dr Angela Molga0 sites100 target enrollmentMarch 2, 2020
ConditionsFrailtyHaematological malignanciesMyelodysplastic syndromeAcute Myeloid LeukemiaMultiple myelomaDiffuse Large B cell LymphomaQuality of lifePolypharmacyCancer - Leukaemia - Acute leukaemiaCancer - Lymphoma (non Hodgkin's lymphoma) - High grade lymphomaCancer - MyelomaCancer - Other cancer typesBlood - Haematological diseasesPublic Health - Health service research
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Frailty
- Sponsor
- Dr Angela Molga
- Enrollment
- 100
- Status
- Not yet recruiting
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients must satisfy the following criteria to be enrolled in the study:
- •·Age 65 years or older
- •·Diagnosis of haematological malignancy according to relevant classification system
- •oLymphoma –diffuse B\-cell lymphoma (DLBCL)
- •oMultiple myeloma – for first line treatment or first relapse
- •oMyelodysplastic syndrome (MDS) and acute myeloid leukemia (AML)
- •·Ability to provide informed consent. If patients are from a non\-english speaking background, informed consent will be determined using an interpreter and including carers
- •·Able to participate in study assessments
- •·Life expectancy predicted by the clinician to be over 6 months
- •·If therapy has commenced at the time of enrollment, then baseline assessments must be completed within 7 days of commencement of therapy
Exclusion Criteria
- •·Age \<65 years of age
- •·MDS, AML patients previously treated with azacitidine, intensive chemotherapy and/or allogeneic stem cell transplantation
- •·DLBCL and multiple myeloma patients failed 2 lines of treatment
- •·End of life care at time of enrollment
- •·Best supportive care treatment at time of enrollment. Patients can be reconsented if they are then determined for active therapy and meet all other inclusion criteria.
- •·Enrollment on any other study where non\-interventional studies are prohibited
- •·Any significant condition that would confound the collection or interpretation of data from the study
- •·Unable or unwilling to provide consent
Outcomes
Primary Outcomes
Not specified
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