Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
Healthy Volunteers
NCT02671448

Pilot Trial of Homebound Stem Cell Transplantation

Led by Memorial Sloan Kettering Cancer Center · Updated on 2026-02-05

91

Participants Needed

1

Research Sites

574 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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).

CONDITIONS

Official Title

Pilot Trial of Homebound Stem Cell Transplantation

Who Can Participate

Age: 18Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of Plasma cell dyscrasia
  • Treatment plan including Autologous HSCT
  • Age between 18 and 80 years
  • Appropriate homebound setting defined as:
    • Lodging at the MSK Residence, or
    • Staying at home or a "home equivalent" within specified zip codes passing the Home Environment Screening Tool
  • Adequate caregiver support with one or more informal caregivers able to provide 24/7 supervision and complete transplant caregiver education
  • Access to Wi-Fi connection
  • Appropriate third party payer coverage for Homebound Stem Cell Transplant Program
  • Both patient and caregiver willing and able to give informed consent
Not Eligible

You will not qualify if you...

  • Active infection of grade 3 or higher (viral, bacterial, or fungal) before starting preparative regimen
  • Uncontrolled arrhythmias
  • Active or uncontrolled pulmonary disease
  • Karnofsky Performance Scale (KPS) score less than 80
  • Sorror Co-morbidity index 4 or greater except for patients with history of resected cancers
  • Creatinine clearance less than 50 cc/minute
  • Inability of patient or caregiver to speak or read English
  • Inadequate housing arrangements
  • Inadequate caregiver arrangements

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Memorial Sloan Kettering Cancer Center

New York, New York, United States, 10065

Actively Recruiting

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Research Team

H

Heather Landau, MD

CONTACT

S

Sergio Giralt, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

N/A

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SCREENING

Number of Arms

1

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