Clinical trial

Neurological Impact of Weight Reduction and Fitness Interventions

Opening soon · Not applicable · 1 countries · Registry ID NCT06830252

Opening soonNot applicableInterventional

What this study is about

This study will test how significant weight loss through bariatric surgery, combined with a personalised exercise program, affects brain inflammation. Th investigators want to understand the connection between obesity-related body inflammation, metabolic issues, and brain inflammation and function.

A promising-looking record is not the same as confirmed eligibility. The study team must review the full criteria and current recruitment status.

Basic eligibility

Age18 Years to 80 Years
SexAll
Healthy volunteersNot accepted
ConditionObesity and Overweight

Full registry criteria

Inclusion Criteria: * 18-80 years of age. * Eligible for bariatric surgery. * Willingness to provide informed consent and willingness to participate and comply with the study requirements Exclusion Criteria: * Unable to undertake MRI due to size restrictions i.e., shoulder width more than 70 cm. * History or clinical manifestation of any other significant metabolic, hematologic, pulmonary, cardio- vascular, gastrointestinal, neurologic, immune, hepatic, renal, urologic, muscular, and joint disorders, or cancer that, in the opinion of the investigator, would make the candidate ineligible for the study. For example, significant joint pain could interfere with adherence to the exercise program. * Have objectively assessed cognitive impairment as assessed by the Montreal Cognitive Assessment (MoCA) i.e., total score less than 26. * Non-MRI-compatible implanted devices or implants. * Inability to exercise via supine ergometer. * Claustrophobia. * Psychiatric or behavioural problems (history of drug and alcohol abuse, eating disorder). * Breastfeeding or pregnant women, or those intending to become pregnant before the scheduled end of the intervention. * Unwilling to be assigned at random to the exercise or control intervention. * Unwilling or unable to adhere to the rigors of the exercise intervention or evaluation schedule over the entire one-year period. * Concurrent participation in any other interventional study.

Treatments and study arms

Exercise

Behavioral

Exercise.

Primary outcomes

Markers of neuroinflammationBaseline and 12 months after surgery.

Between intervention and control at 12 months after surgery. Assessed via DBSI-MRI.

Study locations

1 locations were listed when this page was built. The first 40 are shown.

Charles Perkins Centre Clinic🇦🇺 Royal Prince Alfred Hospital, New South Wales, Australia
Study CoordinatorContact
Principal InvestigatorContact
Study CoordinatorSub Investigator