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Experimental for Breast Reconstruction (RESTORE Trial)
N/A
Waitlist Available
Led By Sophocles Voineskos, MD, MSc.
Research Sponsored by McMaster University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Women 18 years of age or older
Able to understand and communicate in English
Timeline
Screening 3 weeks
Treatment Varies
Follow Up this will be calculated through study completion, an average of 1 year, at the time when every enrolled participant is set to complete the final follow up.
Awards & highlights
RESTORE Trial Summary
Educational Session To Optimize Patient's Breast Reconstruction Experience at McMaster
Eligible Conditions
- Breast Reconstruction
- Patient Education
RESTORE Trial Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowRESTORE Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ this will be calculated through study completion, an average of 1 year, at the time when every enrolled participant is set to complete the final follow up.
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~this will be calculated through study completion, an average of 1 year, at the time when every enrolled participant is set to complete the final follow up.
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Feasibility of the research study as measured by retention rate
Secondary outcome measures
Anxiety
Feasibility measure: Budget assessment
Feasibility measure: Compliance rate
+7 moreRESTORE Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: ExperimentalExperimental Treatment1 Intervention
The experimental group will receive an additional educational session before their operation about what to expect during their reconstructive journey, in addition to the current standard educational information from the surgeon along with an information package.
Group II: ControlActive Control1 Intervention
The control group will receive the current standard educational information from the surgeon along with an information package.
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Who is running the clinical trial?
McMaster UniversityLead Sponsor
879 Previous Clinical Trials
2,596,926 Total Patients Enrolled
1 Trials studying Breast Reconstruction
722 Patients Enrolled for Breast Reconstruction
Sophocles Voineskos, MD, MSc.Principal InvestigatorMcMaster University
Frequently Asked Questions
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