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Measuring Patient Satisfaction and Quality of Life Following Body Image Altering Surgery

Measuring Patient Satisfaction and Quality of Life Following Body Image Altering Surgery: Development and Validation of a Patient-Reported Outcomes Instrument

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00605670
Enrollment
722
Registered
2008-01-31
Start date
2005-06-30
Completion date
2013-11-30
Last updated
2013-11-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Augmentation, Breast Cancer, Breast Reconstruction, Breast Reduction, Breast Surgery

Brief summary

The goal of this study is to develop a questionnaire to measure patient satisfaction with their breast surgery. This questionnaire will help surgeons better understand how patients feel about their surgical results. We hope that such a questionnaire will improve the understanding of breast surgery results and patient care.

Interventions

BEHAVIORALquestionnaires

patients will fill out two questionnaires post surgery

Sponsors

McMaster University
CollaboratorOTHER
University College, London
CollaboratorOTHER
Dartmouth-Hitchcock Medical Center
CollaboratorOTHER
University of British Columbia
CollaboratorOTHER
Johns Hopkins University
CollaboratorOTHER
University of Pittsburgh
CollaboratorOTHER
Memorial Sloan Kettering Cancer Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* All stages (1-4) * Age \> or = to 18 to 85 years. * Postoperative Group: Male and Female patients who have undergone mastectomy, breast reconstruction, reduction, augmentation, bariatric or body contouring surgery between 1 month to 8 years ago Or * Preoperative Group: Male and Female patients who are scheduled to undergo mastectomy, breast reconstruction, reduction, or augmentation or body contouring surgery

Exclusion criteria

* Inability to speak or understand English * Active psychiatric illness, cognitive or sensory impairment * Physical impairment that may prevent filling out a paper and pencil survey or responding to interview questions

Design outcomes

Primary

MeasureTime frame
To develop and validate a new patient derived measure of satisfaction with breast surgery.conclusion of study

Secondary

MeasureTime frame
Determining variations in satisfaction related to patient characteristics and preoperative expectations.conclusion of study

Countries

Canada, United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026