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Screening for Gynecologic Cancers in Hereditary Nonpolyposis Colorectal Cancer (HNPCC) Patients

Completed
Conditions
Colon Cancer
Interventions
Behavioral: Questionnaire
Registration Number
NCT00508846
Lead Sponsor
M.D. Anderson Cancer Center
Brief Summary

Among women with HNPCC, this study will assess:

1. Knowledge of screening recommendations for endometrial and ovarian cancers.

2. Perceived risk and cancer worries regarding endometrial, ovarian and colorectal cancers.

3. Adherence to screening recommendations for endometrial, ovarian and colon cancers.

4. Perceived benefits,supports and barriers to endometrial and ovarian cancer screening.

5. Patterns of communication about endometrial and ovarian cancer risk within families with HNPCC and with health care providers.

6. Patient preferences for potential cancer screening and cancer prevention strategies related to HNPCC-associated cancers.

Detailed Description

Women who are at risk for HNPCC will be recruited to participate in this pilot study.

Women will be invited to participate in the study either through a mailed invitation or during a visit to M.D. Anderson for clinical services or for research purposes.

Women who wish to participate in the study will complete an informed consent, and will subsequently schedule an appointment with a research coordinator to complete the study questionnaire by telephone.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
93
Inclusion Criteria
  1. Being female
  2. Being 25 years of age or older
  3. Having an HNPCC-predisposing mutation and/or having a family history of cancer that meets the Amsterdam or Amsterdam II criteria for HNPCC
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Exclusion Criteria
  1. Persons who have tested negative for a known HNPCC-predisposing mutation in their family
  2. Persons who have no family HNPCC mutation and have not met the Amsterdam I/II criteria
  3. Being younger than 25 years old
  4. Note: Women who have had a prior history of colorectal cancer or polyps will not be excluded unless they meet one of the above exclusion criteria.
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
HNPCC PatientsQuestionnaire-
Primary Outcome Measures
NameTimeMethod
Patient Responses to Questionnaire7 Years

Outcomes measuring demographics, surveillance behaviors, perceived risk, and cancer worries, screening supports/benefits and barriers.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Texas MD Anderson Cancer Center

🇺🇸

Houston, Texas, United States

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