Quality of Life Among Breast Reduction Patients

Sponsor
Hamilton Health Sciences Corporation (Other)
Overall Status
Completed
CT.gov ID
NCT00149370
Collaborator
(none)
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Study Details

Study Description

Brief Summary

Despite the growing evidence showing that breast hypertrophy is associated with reduced Health-Related Quality of Life (HRQL) and that reduction mammoplasty has a significant positive impact on HRQL, there are unresolved issues that need to be addressed. These include our ability to measure quantitatively the change that occurs after reduction and the ongoing restriction or denials of third party payments based on body mass index (BMI). The primary purpose of this study is to assess and measure the HRQL experienced by breast reduction patients using four reliable and validated HRQL measures.

Fifty-two consecutive patients with the diagnosis of breast hypertrophy were invited to participate in this prospective study. Participants completed the Health Utilities Index Mark 2 (HUI2) and Mark 3 (HUI3) and the Breast Reduction Assessment Value and Outcomes (BRAVO) instruments (the Short Form 36, the Multidimensional Body-Self Rating Questionnaire Appearance Assessment, and the Breast Related Symptom Questionnaire) at one week and one day pre-surgery and one, six, and 12 months post-surgery.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Breast reduction surgery

Detailed Description

This study addresses the following questions of clinical and policy relevance: 1) Is the pre-surgery HRQL of these patients compromised and, if so, in which areas? 2) Do patients' HRQL improve after surgery and, if so, when and in which areas and by how much? 3) Is there a relationship between BMI and pre-/post-surgery changes in HRQL (i.e., is the pre/post effect similar for both obese and non-obese patients)? and 4) Is there a relationship between tissue re-section weight and pre-/post-surgery changes in HRQL (i.e., is the pre/post HRQL effect similar for patients having small and large amounts of tissue resected)?

Study Design

Study Type:
Observational
Observational Model:
Defined Population
Time Perspective:
Prospective
Official Title:
A Prospective Study of Patients Undergoing Breast Reduction Surgery: Health-Related Quality of Life and Clinical Outcomes
Study Start Date :
Jan 1, 2001
Study Completion Date :
Aug 1, 2003

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Diagnosis of breast hypertrophy

    • Government approval for payment of reduction mammoplasty

    Exclusion Criteria:
    • Unable or unwilling to complete the quality of life questionnaires

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 St. Joseph's Healthcare / McMaster University Hamilton Ontario Canada L8N 4A6

    Sponsors and Collaborators

    • Hamilton Health Sciences Corporation

    Investigators

    • Principal Investigator: Achilleas Thoma, MD MSc FRCSC, McMaster Univeristy / St. Joseph's Healthcare

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00149370
    Other Study ID Numbers:
    • 02-09-2005
    First Posted:
    Sep 8, 2005
    Last Update Posted:
    Sep 8, 2005
    Last Verified:
    Aug 1, 2005

    Study Results

    No Results Posted as of Sep 8, 2005