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Presurgical Counseling for Weight Loss
N/A
Waitlist Available
Led By Tiffany Tanner, MD
Research Sponsored by University of Nebraska
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up presurgical, 3 mos, 6 mos
Awards & highlights
Study Summary
This trial is testing whether children of mothers who have received bariatric surgery are more likely to have healthier weights themselves.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ presurgical, 3 mos, 6 mos
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~presurgical, 3 mos, 6 mos
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Child weight loss
Maternal weight loss
Secondary outcome measures
Child Activity Level
Child diet
Maternal Activity level
+1 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Mother-Child with InterventionExperimental Treatment1 Intervention
Children will attend presurgical visits with their mother
Group II: Mother-Child Non-InterventionActive Control1 Intervention
Children will not attend presurgical visits with their mother
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Presurgical Counseling
2019
N/A
~10
Find a Location
Who is running the clinical trial?
University of NebraskaLead Sponsor
536 Previous Clinical Trials
1,143,917 Total Patients Enrolled
5 Trials studying Weight Loss
619 Patients Enrolled for Weight Loss
Tiffany Tanner, MDPrincipal Investigator - UNMC
Nebraska Health System-University Hospital
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