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This document presents research findings on the demographic profiles and inquiries of users contacting the National Cancer Institute’s Cancer Information Service from 2003 to 2008, highlighting
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How to fill out Profiles of 800,000 Users of the National Cancer Institute’s Cancer Information Service Since the Debut of Online Assistance, 2003-2008

01
Gather the necessary data from the Cancer Information Service database.
02
Ensure that you have access to the profiles of the 800,000 users from 2003 to 2008.
03
Review the specific fields required for each user profile (e.g., demographics, cancer-related information).
04
Develop a standardized format or template for inputting the data to maintain consistency.
05
Begin data entry process, starting with the earliest profiles to the latest ones.
06
Double-check each profile for accuracy and completeness.
07
Utilize automated tools if available to expedite the filling process.
08
Regularly back up the data to prevent loss during the data entry process.
09
Complete the profiles with any additional relevant information if available.
10
Implement a review and quality assurance process to validate the filled profiles.

Who needs Profiles of 800,000 Users of the National Cancer Institute’s Cancer Information Service Since the Debut of Online Assistance, 2003-2008?

01
Researchers studying cancer trends and demographics.
02
Public health officials looking for data to inform cancer prevention strategies.
03
Healthcare providers seeking insights into patient profiles for tailored treatments.
04
Policy makers aiming to improve cancer-related health policies.
05
Non-profit organizations focused on cancer awareness and support.
06
Educational institutions conducting studies on cancer information dissemination.
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August 5, 1937—The National Cancer Institute (NCI) was established through the National Cancer Act of 1937, signed into law by President Franklin D. Roosevelt. Its passage represented the culmination of nearly three decades of efforts to formalize the U.S. government's place in cancer research.
Leadership No.DirectorTenure 16 Monica Bertagnolli October 17, 2022 – November 9, 2023 – Douglas R. Lowy (acting) November 10, 2023–December 17, 2023 17 Kimryn Rathmell December 18, 2023 – January 20, 2025 – Douglas R. Lowy (acting) January 21, 2025–present21 more rows
National Cancer Institute The "comprehensive" designation from the NCI is the world's most prestigious institutional honor in oncology and awarded to only about one percent of cancer centers nationwide.
The NCI-Designated Cancer Centers are recognized for their scientific leadership in laboratory and clinical research, in addition to serving their communities and the broader public by integrating training and education for biomedical researchers and health care professionals.
The National Cancer Institute (NCI) is the federal government's principal agency for cancer research and training. Established under the National Cancer Institute Act of 1937, NCI is part of the National Institutes of Health (NIH), one of 11 agencies that make up the Department of Health and Human Services (HHS).
The National Cancer Institute (NCI) is the federal government's principal agency for cancer research and training. Our team of approximately 3,500 is part of the National Institutes of Health (NIH), one of 11 agencies that make up the Department of Health and Human Services (HHS).
NCI is the nation's trusted source for cancer information.

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The Profiles of 800,000 Users of the National Cancer Institute’s Cancer Information Service is a comprehensive collection of data regarding individuals who accessed cancer information services online from 2003 to 2008. This dataset includes information on user demographics, the type of services accessed, and feedback on the assistance provided.
Individuals or organizations involved in gathering, analyzing, or reporting data on the usage of the National Cancer Institute’s Cancer Information Service are required to file these profiles. This may include researchers, healthcare professionals, or organizations collaborating with the National Cancer Institute.
To fill out the profiles, users must collect relevant data from their interactions with the Cancer Information Service, ensuring to include demographic information, the nature of inquiries, and outcomes of the assistance received. Detailed guidelines for the format and required fields are typically provided by the National Cancer Institute.
The purpose of these profiles is to analyze and improve cancer information services, understand user needs, enhance outreach programs, and contribute to research aimed at better supporting individuals seeking information on cancer.
The information that must be reported includes user demographics (age, gender, geographic location), types of inquiries made, the services accessed, user satisfaction ratings, and any reported outcomes from the information provided.
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