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CompletedNCT01504152Updated Jul 12, 2013

International Travel Patterns and Health Preparations of Hematopoietic Stem Cell Transplant Recipients at Memorial Sloan-Kettering Cancer Center

An observational study in Hematopoietic Stem Cell Transplant, sponsored by Memorial Sloan Kettering Cancer Center. Completed at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2013-07-12.

Sponsored by Memorial Sloan Kettering Cancer Center · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
519
Ages
18 Years and older
Sex
All
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Study summary

The purpose of this study is to survey patients who underwent hematopoietic stem cell transplant (HSCT) to assess if they have traveled or not internationally after transplant. This information will help to improve the understanding of the needs for travel health strategies and interventions to provide healthy and safe travel to HSCT patients. The findings of this survey will also be used to develop travel health related interventions for patients living with cancer as well.

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Conditions studied

  • Hematopoietic Stem Cell Transplant

Keywords

  • International travel
  • cancer patients
  • HSCT
  • Quality of Life
  • questionnaire
  • 11-176
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In context

Lead sponsor

Memorial Sloan Kettering Cancer Center is the lead sponsor of 1,930 studies on the registry; 328 are open to participants now.

Of its 129 completed or terminated interventional studies of FDA-regulated products, 66 (51%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients who received HSCT at MSKCC between 2005-2010 and were alive after the first year after HSCT.

Inclusion criteria

  • Hematopoietic Stem Cell Transplant (HSCT) recipients at MSKCC from 1/1/2005 to 12/31/2010.
  • Age at HSCT ≥ 18 years
  • Permanent mailing address in the United States of America

Exclusion criteria

Exclusion Criteria:

  • Subject unable to fill the questionnaire due to language barriers.
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Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
519 participants (actual)

Groups and cohorts

  • patients who received HSCT at MSKCC between 2005-2010

    A self-administered patient questionnaire will be used to collect data that will assess the prevalence of international travel after HSCT and travel related morbidity and exposure risks among HSCT recipients.

    Behavioral: questionnaire

Interventions

  • Behavioralquestionnaire

    The intervention is a self-administered questionnaire that is voluntarily completed by the subject. This questionnaire has been previously validated and demonstrated to be reproducible in English speaking travelers. The final version of the survey questionnaire consists of 49 questions.Patients who never traveled after HSCT will answer only eighteen questions related to their medical and HSCT history in addition to their demographics.

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What researchers measure

Primary outcomes

  1. prevalence of international travel

    of the targeted patients Proportion of Hematopoietic Stem Cell Transplant (HSCT) patients who traveled internationally within two years after HSCT

    Time frame: 2 years

Secondary outcomes

  1. international travel was during a high-risk specific period

    Proportion of patients traveling to destinations that are at high risk areas for infections

    Time frame: 2 years

  2. patients that sought pre-travel health advice

    among those who traveled to high risk areas for infections

    Time frame: 2 years

  3. travelers that becomes ill and required medical attention

    during or after return from international travel.

    Time frame: 2 years

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Study locations

1 site
  • Memorial Sloan-Kettering Cancer Center
    New York, New York 10065, United States
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References and documents

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 12, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01504152
Lead sponsor
Memorial Sloan Kettering Cancer Center
Collaborators
Weill Medical College of Cornell University
Responsible party
Sponsor
First posted
Jan 5, 2012
Start date
Dec 2011
Primary completion
Jul 2013
Completion
Jul 2013
Last update
Jul 12, 2013

Study contacts

Monika Shah, MD
principal investigator · Memorial Sloan Kettering Cancer Center
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2013. You cannot join it, but the record below documents what was studied.

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