Pilot Trial of Homebound Stem Cell Transplantation

Plasma Cell Dyscrasia Clinical Trial

Official title:

Pilot Trial of Homebound Stem Cell Transplantation

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02671448
• Other study ID #: 15-022
• Status: Recruiting
• Phase: N/A
• Start date: January 2016
• Est. completion date: January 2025

Study information

• Verified date: February 2024
• Source: Memorial Sloan Kettering Cancer Center
• Contact: Heather Landau, MD
• Email: ABMTTrials[@]mskcc.org
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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).

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 91
• Est. completion date: January 2025
• Est. primary completion date: January 2025
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

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

Related Conditions & MeSH terms

• Multiple Myeloma
• Neoplasms, Plasma Cell
• Paraproteinemias
• Plasma Cell Dyscrasia

Intervention

Behavioral:
• Home monitoring teleconsult visits
A tablet will be provided to both the patient and the caregiver during the homecare portion of the study. The tablet will remain at the home, to be used by the patient and the caregiver during daily homecare visits to complete instruments/surveys and video diary recording sessions.
• Patient Reported Outcomes (PRO)
Distress Thermometer, MSK-Modified M.D. Anderson Symptom Inventory (MDASI) Instrument, FACT-G Instrument, FACT-BMT Instrument
• Caregiver Reported Outcomes instruments
Distress Thermometer, Caregiver Reaction Assessment (CRA) Instrument, The Caregiver Quality of Life Index-Cancer (CQOLC) Scale, Satisfaction Questionnaire, Video Diary Entries

Locations

Country	Name	City	State
United States	Memorial Sloan Kettering Cancer Center	New York	New York

Sponsors (1)

Lead Sponsor	Collaborator
Memorial Sloan Kettering Cancer Center

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	readmission rate by 21 days post HSCT	the homebound procedure will be considered promising if no more than 10 patients are readmitted to the hospital within 21 days.	21 days post HSCT

External Links

•   Memorial Sloan Kettering Cancer Center