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Multidisciplinary Health Intervention for Blood Cancer
N/A
Waitlist Available
Led By Andrew S Artz
Research Sponsored by City of Hope Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Hematologic malignancy or disease as indication for HCT
>= 65 years at time of planned HCT infusion
Must not have
Prior allogeneic stem cell transplant
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 1 year
Awards & highlights
No Placebo-Only Group
Summary
This trial is studying a multidisciplinary intervention to help older adults with blood cancers who are planning a stem cell transplant. The intervention includes multiple healthcare professionals and is aimed at improving fitness and the ability to bounce back after transplant.
Who is the study for?
This trial is for older adults (65+) with blood cancers who are candidates for stem cell transplantation. Participants must be able to read English, Spanish, or Mandarin and consent to the study's requirements. Those with prior allogeneic transplants or conditions that make study procedures unsafe are excluded.
What is being tested?
The trial is testing a multidisciplinary approach involving various healthcare professionals aimed at improving fitness and recovery post-transplant in older adults. It includes health promotion activities, quality-of-life assessments, and questionnaires.
What are the potential side effects?
Since this trial focuses on non-medical interventions like health promotion and questionnaires rather than drugs or medical treatments, traditional side effects are not applicable. However, participants may experience fatigue or stress related to additional appointments.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I need a stem cell transplant for my blood cancer.
Select...
I am 65 years or older.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have had a stem cell transplant from a donor.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 1 year
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 1 year
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Feasibility of multidisciplinary team (MDT) (met 90 percent threshould, yes / no)
Secondary study objectives
Dose intensity of resiliency bolstering
Functional independent survival (FIS)
Library of MDT-facilitated intervention
+1 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Supportive care (MDT-intervention)Experimental Treatment3 Interventions
Patients participate in the MDT-intervention including access to a HCT physician, a geriatrician, physical or occupational therapist, dietician, and a social worker for three months before HCT and up to 100 days after HCT.
Find a Location
Who is running the clinical trial?
City of Hope Medical CenterLead Sponsor
602 Previous Clinical Trials
1,923,540 Total Patients Enrolled
National Cancer Institute (NCI)NIH
13,928 Previous Clinical Trials
41,018,020 Total Patients Enrolled
2 Trials studying Blood Cancers
112 Patients Enrolled for Blood Cancers
Andrew S ArtzPrincipal InvestigatorCity of Hope Comprehensive Cancer Center
1 Previous Clinical Trials
164 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I can read English, Spanish, or Mandarin, or another language if the study allows it.I can have any type of preparation treatment and any donor for my transplant.I need a stem cell transplant for my blood cancer.I have had a stem cell transplant from a donor.I am 65 years or older.I am willing and able to follow the study's requirements.My doctor thinks I am a good candidate for a stem cell transplant from a donor.
Research Study Groups:
This trial has the following groups:- Group 1: Supportive care (MDT-intervention)
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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