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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01111201
Other study ID # 10-045
Secondary ID
Status Completed
Phase N/A
First received April 22, 2010
Last updated May 30, 2012
Start date April 2010
Est. completion date March 2012

Study information

Verified date May 2012
Source Memorial Sloan Kettering Cancer Center
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

This study also aims to raise awareness among both patients and health-care providers about the importance of pre-travel health consultation and preventive interventions prior to international travel.

Through appropriate health counseling, cancer patients will have less risk of having travel -related health complications and thus have a better quality of life and overall improved sense of wellbeing.


Recruitment information / eligibility

Status Completed
Enrollment 26
Est. completion date March 2012
Est. primary completion date March 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Hematopoietic Stem Cell Transplant (HSCT) recipients

- Age >18 years

- Status post bone marrow transplant within last five years Breast Cancer patients: Criteria 1 and Criteria 2 and/or 3

- Female age >18 years and current or past history of breast cancer

- Received systemic chemotherapy in the last five years

- Metastatic breast cancer disease (stage IV) Lymphoma: Criteria 1 and Criteria 2 and/or 3

- Age >18 years and current or past history of lymphoma

- Received systemic chemotherapy within 5 years

- Had active disease at any time within the last 5 years

Exclusion Criteria:

- Patients age< 18 years

- Breast cancer and lymphoma patients in clinical remission in the past 5 years

- Patients unable to fill the questionnaire due to language barriers

Study Design

Observational Model: Cohort, Time Perspective: Retrospective


Related Conditions & MeSH terms


Intervention

Behavioral:
questionnaires
The intervention is a self-administered anonymous questionnaire that is voluntarily completed by the patient. Questions in Section One will cover general information about the patient including gender, age, race, country of birth, current zip code of residence, and level of education. Questions in Section Two will cover information regarding the cancer (breast/lymphoma) or transplant (allogeneic/ autologous). Questions in Section Three will cover travel history including the frequency of travel outside the United States and Canada in the last 5 years. Questions in Sections Four through Seven will obtain information about their last trip outside the United States and Canada.

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 To determine the frequency of international travel of the targeted patients in the last 5 years. once at the time of the clinic visit No
Secondary To determine if any of the international travel was during a high-risk specific period when the immune status of the target population was compromised. once at the time of the clinic visit No
Secondary To profile the target population who traveled internationally with respect to their demographic and cancer/transplant-related characteristics. once at the time of the clinic visit No
Secondary To obtain detailed information about their last international trip including once at the time of the clinic visit No
Secondary To assess the adequacy of the questionnaire instructions once at the time of the clinic visit No
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