NCT00476632

Brief Summary

The goal of this research study is to identify biologic and lifestyle factors that may increase a person's risk of developing certain types of cancer.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
1,500

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jun 2004

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 1, 2004

Completed
3 years until next milestone

First Submitted

Initial submission to the registry

May 21, 2007

Completed
1 day until next milestone

First Posted

Study publicly available on registry

May 22, 2007

Completed
12 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2019

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2019

Completed
Last Updated

May 10, 2019

Status Verified

May 1, 2019

Enrollment Period

15 years

First QC Date

May 21, 2007

Last Update Submit

May 8, 2019

Conditions

Healthy

Keywords

EpidemiologyQuestionnaireControls

Outcome Measures

Primary Outcomes (1)

  • To identify biologic and lifestyle factors that may increase a person's risk of developing certain types of cancer.

    6 Years

Study Arms (1)

Control

Person with no history of cancer.

Behavioral: Questionnaire

Interventions

QuestionnaireBEHAVIORAL

50 Minute Interview

Also known as: Survey
Control

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Individuals 18 years or older with no history of cancer.

You may qualify if:

  • Individuals ages 18 and over with no prior cancer
  • Willing and able to complete an administered questionnaire
  • Willing and able to donate 30 mL of blood

You may not qualify if:

  • Individuals with prior cancer
  • Individuals under the age of 18

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Texas MD Anderson Cancer Center

Houston, Texas, 77030, United States

Location

Related Links

Biospecimen

Retention: SAMPLES WITH DNA

2 ½ tablespoons of blood drawn.

MeSH Terms

Interventions

Surveys and Questionnaires

Intervention Hierarchy (Ancestors)

Data CollectionEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Study Officials

  • Carrie Daniel-MacDougall, PHD

    M.D. Anderson Cancer Center

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 21, 2007

First Posted

May 22, 2007

Study Start

June 1, 2004

Primary Completion

June 1, 2019

Study Completion

June 1, 2019

Last Updated

May 10, 2019

Record last verified: 2019-05

Locations

US(1)