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The Collateral Impact of Bariatric Surgery on Families

The Collateral Impact of Bariatric Surgery on Families

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02021630
Acronym
Collateral
Enrollment
97
Registered
2013-12-27
Start date
2012-12-31
Completion date
2016-07-31
Last updated
2016-10-21

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

Conditions

Bariatric Surgery Candidate, Obesity, Weight Loss

Keywords

Obesity, Bariatric Surgery, Weight Loss, Physical Activity, Body Composition

Brief summary

This proposal is designed to examine the impact of bariatric surgery on the health of patients and their families. The shared environment of spouses/cohabitating partners suggests that patients' families are exposed to the extensive diet and lifestyle changes required of patients following bariatric surgery.

Detailed description

The specific aims of this proposal are to: 1. Collect clinical data (e.g., weight, blood pressure, body composition, blood sample), as well as monitor physical activity and eating patterns, before and after bariatric surgery (Adults Only). 2. Analyze clinical data, physical activity and eating patterns to determine how the health of patients and their families change after one family member completes bariatric surgery (Adults Only). 3. Determine the feasibility of recruiting patients, spouses/partners and their children.

Interventions

OTHEROutcomes

No intervention will occur during this study. Evaluation of changes in patients' family after having patient has bariatric surgery.

Sponsors

Geisinger Clinic
Lead SponsorOTHER

Study design

Observational model
FAMILY_BASED
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* All patients who receive surgery have been cleared medically and psychosocially for surgery. Thus, surgical candidacy criteria will serve as eligibility criteria for the current study for surgical patients. * Cohabitation with patients will be considered inclusion criteria for partners/spouses. * Children between the ages of ≥5 - ≤ 16, who cohabitate with the patient the majority of the time will be asked to participate by providing assent.

Exclusion criteria

* Report current or planned use of weight loss medications (including OTC), or other weight loss strategy. * Report pregnancy, lactation, or plans to become pregnant during study duration.

Design outcomes

Primary

MeasureTime frame
WeightPre-operatively, post-operatively 6 months and 12 months

Secondary

MeasureTime frameDescription
Percent body fatPre-operatively, post-operatively 6 months and 12 months
Physical ActivityPre-operatively, post-operatively 6 months and 12 monthsAccelerometer

Other

MeasureTime frameDescription
Laboratory outcomesPre-operatively, post-operatively 6 months and 12 monthsLipid panel, insulin, glucose
QuestionnairesPre-operatively, post-operatively 6 months and 12 monthsHome Food Inventory, Social Support

Countries

United States

Outcome results

None listed

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