Mother and Child Health Outcomes After Maternal Bariatric Surgery
NCT ID: NCT03297307
Last Updated: 2023-09-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
5 participants
INTERVENTIONAL
2019-01-01
2022-09-02
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Female Fertility Outcome Following Bariatric Surgery: Five Years Follow up
NCT04392661
Survey on Patients After Childbearth Following Bariatric Surgery
NCT04297956
The Collateral Impact of Bariatric Surgery on Families
NCT02021630
Monitoring Nutritional Consequences of Obesity Treatment on Women's Health
NCT06945016
Effect of Personalized Nutrition Counseling in Pregnant Women After Bariatric Surgery on Nutritional Status and Habits
NCT02697981
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Each bariatric surgical patient will receive a consultation with a dietician, psychologist, and an exercise physiologist as standard-of-care. These specialist consultations usually take place sequentially in the same day. The intervention aspect of this study is to include the child with the mother for these specialist consultations. The dietician will educate the patient as to dietary modifications that will be needed both before and after bariatric surgery. The psychologist will review any existing psychological conditions with the patient and discuss behavioral and pharmaceutical management of these conditions in conjunction with the bariatric surgery. The exercise physiologist will discuss physical restrictions to exercise and modifications to an exercise regimen that can be properly performed by the patient.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NON_RANDOMIZED
SINGLE_GROUP
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Mother-Child with Intervention
Children will attend presurgical visits with their mother
Presurgical Counseling
Children will attend the presurgical counseling visits with their mother
Mother-Child Non-Intervention
Children will not attend presurgical visits with their mother
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Presurgical Counseling
Children will attend the presurgical counseling visits with their mother
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. Consent to provide access to medical records for medical history
3. Will receive weight loss procedure (sleeve gastrectomy or gastric bypass) at Nebraska Medicine
4. Have children ages 8-17 (at the time of the mother's surgery) living in the home
5. Consent to wear an activity tracker device for 7 days after designated visits.
Exclusion Criteria
2. Body contouring within the first year (panniculectomy, etc.).
3. Are pregnant or become pregnant during the study
19 Years
55 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Nebraska
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Tiffany Tanner, MD
Role: PRINCIPAL_INVESTIGATOR
UNMC
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
University of Nebraska Medical Center
Omaha, Nebraska, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
0821-17-EP
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.