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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01003600
Other study ID # 09-133
Secondary ID
Status Completed
Phase N/A
First received October 28, 2009
Last updated November 26, 2014
Start date October 2009
Est. completion date November 2014

Study information

Verified date November 2014
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

We are doing this study to learn more about colon and rectal cancer survivors. We want to know if survivors want more information about life after cancer. Do cancer survivors want to know more about their own cancer? Do cancer survivors want to know about their treatment? Do cancer survivors want to know what health care they should get in the future? We want to know what information to give to cancer survivors when they finish treatment.


Recruitment information / eligibility

Status Completed
Enrollment 177
Est. completion date November 2014
Est. primary completion date November 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- 18 years of age or older at diagnosis

- Diagnosed with first primary colorectal cancer (stage I-III)

- Completed last treatment for colorectal cancer (surgery, chemotherapy, or radiation) at least 6 months and no more than 2 years before the date of study enrollment

- Able to speak English, because questionnaire is only available in English

- Able to provide informed consent

- Received all treatment for colorectal cancer at MSKCC or QCC or, surgical treatment at an outside facility, and all other treatment (chemotherapy or radiation) at MSKCC or QCC

Exclusion Criteria:

- Undergoing active treatment for colorectal cancer

- Diagnosed with metastatic colorectal cancer

- Prior history of colorectal or any other cancer (except non-melanoma skin cancer)

- Diagnosed with new or recurrent colorectal or other cancer after the primary colorectal cancer diagnosis

- Received a survivorship care plan from the treating institution

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Behavioral:
Questionnaire
The questionnaire will be administered by telephone and will take approximately 20-30 minutes. The questionnaire will elicit survivor responses along five domains: knowledge about diagnosis and treatment, knowledge about ongoing risks and recommended testing, history of health care utilization since the end of treatment, preferences for relevant information about these topics, and employment after the end of cancer treatment.

Locations

Country Name City State
United States Queens Cancer Center of Queens Hospital Jamaica New York
United States Memorial Sloan-Kettering Cancer Center New York New York

Sponsors (2)

Lead Sponsor Collaborator
Memorial Sloan Kettering Cancer Center Queens Cancer Center of Queens Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Assess colorectal cancer survivors' basic knowledge of their own cancer history, including date of diagnosis, stage, and treatments received. 6 months to 2 years after completion of treatment No
Secondary Assess survivors' knowledge of medical issues relevant to colorectal cancer survivors. 6 months to 2 years after completion of treatment No
Secondary Describe the types of health care providers that survivors have visited since completing treatment for colorectal cancer. 6 months to 2 years after completion of treatment No
Secondary Assess survivors' preferences for the content, format, and delivery of survivorship care plans. 6 months to 2 years after completion of treatment No
Secondary Assess whether survivors who had concerns about working after cancer treatment spoke with health care professionals about their concerns. 6 months to 2 years after completion of treatment No
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