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NCT05215886Enrolling by invitation

Cognitive Impairment, Obesity, and the Effects of Bariatric Surgery

Source: ClinicalTrials.gov · Last updated 5 Dec 2025

Brief summary (registry, in English)

Study is designed to screen psychological cognitive baseline and retention/improvement after weight loss surgery.

Status (registry)
Enrolling by invitation
Study type
Observational
Enrollment
9500 (estimated)
First submitted
18 Jan 2022
Start date
1 Jan 2022
Primary completion date
31 Dec 2026
Lead sponsor
University of California, Davis
Diseases
Obesity
NCT number
NCT05215886

What you commit to

  • Study type: Observational
  • Planned participants: 9500
  • From 1 Jan 2022 to the primary completion date, 31 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Patients without a history of memory impairment/loss, bariatric surgery, or obesity
    • Patients outside of University of California Davis Health System
    • Patients unable to provide consent

Who the study is looking for

  • Cognitive impairment/decline, memory impairment/loss, or Alzheimer's disease or dementia and bariatric surgery • Cognitive impairment/decline, memory impairment/loss, or Alzheimer's disease or dementia and obesity, and no bariatric surgery history

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of California, Davis Medical Center
Coordinator of this site? Confirm its status
SacramentoUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.