Psychosocial Aspects of Multiple Endocrine Neoplasia (MEN) Syndromes

Sponsor
M.D. Anderson Cancer Center (Other)
Overall Status
Completed
CT.gov ID
NCT00501449
Collaborator
(none)
133
1
160.8
0.8

Study Details

Study Description

Brief Summary

The specific aims of the study include:
  1. Profile the demographic, health-related, psychosocial and behavioral characteristics of adults with MEN1 or MEN2.

  2. Evaluate MEN-specific distress as well as adherence to surveillance regimens among adults with MEN1 or MEN2, and identify associated with those outcomes.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Questionnaire

Detailed Description

The proposed cross-sectional study is intended to obtain information regarding current surveillance behaviors and other psychosocial outcomes among persons affected by the multiple endocrine neoplasia (MEN) 1 or MEN2, which are inherited conditions.

Study participants will include patients who have been seen previously at MDACC for evaluation of MEN1 or MEN2. Because this is the first time investigators are contacting these patients to invite them to participate in psychosocial research, the proposed study also will help determine the feasibility of conducting similar studies in the future.

Investigators anticipate that data gathered from this study will enhance existing knowledge about the psychological and behavioral aspects of the MEN syndromes, and will inform future research efforts directed toward this understudied population.

Study Design

Study Type:
Observational
Actual Enrollment :
133 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Psychosocial Aspects of Multiple Endocrine Neoplasia (MEN) Syndromes
Actual Study Start Date :
May 1, 2007
Actual Primary Completion Date :
Sep 22, 2020
Actual Study Completion Date :
Sep 22, 2020

Arms and Interventions

Arm Intervention/Treatment
Multiple Endocrine Neoplasia (MEN)

Patients with multiple endocrine neoplasia (MEN).

Behavioral: Questionnaire
Mailed packets including cover letter describing purpose of study, study questionnaire, and return envelope.
Other Names:
  • Survey
  • Outcome Measures

    Primary Outcome Measures

    1. Profile the demographic, health-related, psychosocial and behavioral characteristics of adults with MEN1 or MEN2. [3 Years]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Adults age 18 years or older, with a clinical or genetic diagnosis of MEN1 or MEN2

    2. Spouse, Significant Other, or Family Member who is at least 18 years of age and who is related to an individual who is a patient at MDACC and who has been diagnosed with MEN1.

    3. Ability to read and write English

    Exclusion Criteria:
    1. Inability to be contacted via mail (i.e., no contact information on record, incorrect address)

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Texas MD Anderson Cancer Center Houston Texas United States 77030

    Sponsors and Collaborators

    • M.D. Anderson Cancer Center

    Investigators

    • Principal Investigator: Susan Peterson, PhD, M.D. Anderson Cancer Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    M.D. Anderson Cancer Center
    ClinicalTrials.gov Identifier:
    NCT00501449
    Other Study ID Numbers:
    • 2006-0783
    First Posted:
    Jul 16, 2007
    Last Update Posted:
    Nov 18, 2020
    Last Verified:
    Nov 1, 2020
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by M.D. Anderson Cancer Center
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 18, 2020