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Breast Augmentation Rehabilitation Program

Not Applicable
Withdrawn
Conditions
Breast Implants
Surgery, Plastic
Interventions
Behavioral: Rehabilitation
Behavioral: Follow-up
Registration Number
NCT01857765
Lead Sponsor
University of British Columbia
Brief Summary

The purpose of this study is to determine whether implementing a rehabilitation program can improve the post-operative time to pain free living after breast augmentation.

Detailed Description

Not available

Recruitment & Eligibility

Status
WITHDRAWN
Sex
Female
Target Recruitment
Not specified
Inclusion Criteria
  • women who undergo endoscopic transaxillary subpectoral breast augmentation
  • women above the age of 18 years
  • women with a BMI 18-27
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Exclusion Criteria
  • women who underwent previous breast reconstruction (cosmetic or therapeutic)
  • women who underwent previous chest surgery
  • women with previous chest trauma
  • women who underwent previous shoulder/arm surgery
  • women with previous shoulder/arm injury
  • women who smoke
  • women who are Immunocompromised
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
RehabilitationFollow-up-
Standard of CareFollow-up-
RehabilitationRehabilitation-
Primary Outcome Measures
NameTimeMethod
Time to return to baseline as measured on Visual Analogue Scale for painBaseline, six months, and one year after surgery
Secondary Outcome Measures
NameTimeMethod
Time to return to bilateral shoulder baseline range of motionBaseline, six months, and one year after surgery
Change in psychosocial outcomes as measured by the BREAST-Q questionnaireBaseline, six months, and one year after surgery

Trial Locations

Locations (1)

University of British Columbia

🇨🇦

Vancouver, British Columbia, Canada

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