Multiple Myeloma Clinical Trial

Pilot Trial of Homebound Stem Cell Transplantation

Summary

In this study, the investigators plan to see what happens when a person receives care in the home setting. They want to find out if caring for a patient who has been treated with an ASCT in the home setting is feasible. They want to find out what effects good and/or bad this will have on the patient's recovery and treatment after ASCT. Studies in other institutions have shown that providing care in the home setting after ASCT is safe, increases patient satisfaction, and can decrease the risk of infection. It is our hope that this new approach of providing care in the home setting will prove to be a feasible and safe option for patients at Memorial Sloan Kettering Cancer Center (MSK).

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Diagnosis of Plasma cell dyscrasia
Treatment plan including Autologous HSCT
18-80 years of age

Appropriate homebound setting as defined by one of the following:

Lodging at the MSK Residence.
Staying at home or a "home equivalent" in any one of the zip codes as outlined in the appendix. Home equivalent is defined as a residence which may or may not be the primary residence of the patient.
"Home equivalent" must pass the "Home Environment Screening Tool" for homebound stem cell transplantation (not required for other MSK recognized lodging facility).

Adequate caregiver support as defined by:

Single or multiple informal caregivers willing and able to provide 24 hour a day, seven day a week supervision of the transplant recipient in their home or "home-like" environment.
Caregiver willing and able to fulfill the basic stem cell transplant caregiver education requirements as determined by caregiver and healthcare team, including social worker
Have Wi-Fi connection
Appropriate third party payer coverage for "Homebound Stem Cell Transplant Program"
Both patient and caregiver willing to give and sign informed consent.

Exclusion Criteria:

Patients with a documented active infection prior to starting their preparative regimen. This includes grade 3 or higher viral, bacterial, or fungal infection.
Uncontrolled arrhythmias
Active or uncontrolled pulmonary disease
Karnofsky Performance Scale (KPS) score <80
Sorror Co-morbidity index ≥ 4 except in patients with history of resected cancers
Creatinine clearance (calculated or measured) of < 50 cc/minute
Inability of patient or caregiver to speak or read English (we currently do not have the manpower to translate nor staff a multilingual homebound stem cell transplant program with adequate educational materials).
Inadequate housing arrangements
Inadequate caregiver arrangements

Study is for people with:

Multiple Myeloma

Estimated Enrollment:

91

Study ID:

NCT02671448

Recruitment Status:

Recruiting

Sponsor:

Memorial Sloan Kettering Cancer Center

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There is 1 Location for this study

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Memorial Sloan Kettering Cancer Center
New York New York, 10065, United States More Info
Heather Landau, MD
Contact
[email protected]
Sergio Giralt, MD
Contact
[email protected]
Heather Landau, MD
Principal Investigator

How clear is this clinincal trial information?

Study is for people with:

Multiple Myeloma

Estimated Enrollment:

91

Study ID:

NCT02671448

Recruitment Status:

Recruiting

Sponsor:


Memorial Sloan Kettering Cancer Center

How clear is this clinincal trial information?

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