Study of Quality of Life in Older vs. Younger Adult Patients Undergoing Allogeneic Hematopoietic Cell Transplantation for Myelodysplastic Syndromes
Status: | Recruiting |
---|---|
Conditions: | Blood Cancer, Blood Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 55 - Any |
Updated: | 1/19/2019 |
Start Date: | July 23, 2018 |
End Date: | December 2019 |
Contact: | Alisha Mussetter, BS |
Email: | amussett@nmdp.org |
Phone: | 763-406-4863 |
A Multi-Center, Phase II Cross-sectional Study Investigating Quality of Life in Older vs. Younger Adult Patients Undergoing Allogeneic Hematopoietic Cell Transplantation for Myelodysplastic Syndromes: a Companion Study to the CIBMTR 10-CMSMDS-1-Approved Expanded Access Study
This is a multi-center, Phase II, cross-sectional study comparing quality of life (QOL) as
assessed by patient-reported outcomes (PROs) in older (≥65 years) adults vs younger (55-64
years) undergoing allogeneic hematopoietic cell transplantation (HCT) for myelodysplastic
syndromes (MDS).
assessed by patient-reported outcomes (PROs) in older (≥65 years) adults vs younger (55-64
years) undergoing allogeneic hematopoietic cell transplantation (HCT) for myelodysplastic
syndromes (MDS).
Transplant recipients who have met the inclusion and exclusion criteria and from
participating study sites will be asked to complete an online consent and survey for the
study. This survey is the patient-reported outcomes survey and will be used to assess quality
of life. The survey results will then be compared by age group and by time post transplant,
between 6 months and a year post transplant, 1 year to 3 years post transplant, and 3 years
or more post transplant.
participating study sites will be asked to complete an online consent and survey for the
study. This survey is the patient-reported outcomes survey and will be used to assess quality
of life. The survey results will then be compared by age group and by time post transplant,
between 6 months and a year post transplant, 1 year to 3 years post transplant, and 3 years
or more post transplant.
Inclusion Criteria:
In order to be eligible to participate on this study, an individual must meet all of the
following criteria:
1. Underwent an allogeneic HCT for MDS on the 10-CMSMDS-1 protocol
2. Prior consent to research and future contact by the CIBMTR
3. Ability to provide RCI BMT protocol 17-ePRO signed and dated informed consent form
(ICF)
4. Age ≥55 years at time of transplant
5. Fluent in English or Spanish
6. Greater than 6 months post-HCT
Exclusion Criteria:
An individual who meets any of the following criteria will be excluded from participation
on this study.
1. No access to an internet browser or email account
2. Within 6 months of first HCT for MDS on the 10-CMSMDS-1 protocol
We found this trial at
6
sites
Milwaukee, Wisconsin 53226
Principal Investigator: Bronwen Shaw, MD, PhD
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12902 USF Magnolia Dr
Tampa, Florida 33612
Tampa, Florida 33612
(888) 663-3488
Principal Investigator: Joseph Pidala, MD, PhD
H. Lee Moffitt Cancer Center & Research Institute Moffitt Cancer Center in Tampa, Florida, has...
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281 W. Lane Ave
Columbus, Ohio 43210
Columbus, Ohio 43210
(614) 292-6446
Principal Investigator: Sumithira Vasu, MBBS
Ohio State University The Ohio State University’s main Columbus campus is one of America’s largest...
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1275 York Ave
New York, New York 10021
New York, New York 10021
(212) 639-2000
Principal Investigator: Roni Tamari, MD
Memorial Sloan Kettering Cancer Center Memorial Sloan Kettering Cancer Center — the world's oldest and...
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450 Serra Mall
Stanford, California 94305
Stanford, California 94305
(650) 723-2300
Principal Investigator: Lori Muffly, MD, MS
Phone: 650-721-4183
Stanford University Stanford University, located between San Francisco and San Jose in the heart of...
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