Neurobehavioral Contribution to Weight Loss Maintenance: an Interdisciplinary Experimental Study With Noninvasive Brain Modulation

Fecha de inicio: 1 de mayo de 2013

Inclusion Criteria: Men and women age 20-55 years old BMI 30-50 kg/m2 Willing to undergo 10 week supervised VLCD Exclusion Criteria: Obesity due to a known secondary cause (Cushing's syndrome, hypothyroidism, etc) or a history of weight loss surgery Subjects who have a known history of diabetes, fasting blood sugar >125 mg/dl or using any anti-diabetic drugs Changes in lipid lowering or anti-hypertensive regimen within 3 months of screening Hemoglobin <10 g/dL, Creatinine >1.5 mg/dL QT interval >440 ms on EKG Subjects with unstable psychiatric conditions as assessed by a psychologist Allergy or intolerance to components of the mixed meal challenge Additional contraindications to receive transcranial direct current stimulation (tDCS): Personal or family history of seizures, epilepsy or other unexplained loss of consciousness. Current or past history of skin disease or damaged skin on the scalp at the site of stimulation (i.e. eczema, skin with ingrown hairs, acne, razor nicks, wounds that have not healed, recent scar tissue, broken skin, etc.). Prior neurosurgical procedure or radiation treatment to the brain. Known diagnosis of brain lesions, such as tumor, stroke or multiple sclerosis Implanted pacemaker, medication pump, vagal stimulator, deep brain stimulator, TENS unit, ventriculoperitoneal shunt or any metallic implant on the head. (Note: Intake of centrally acting medications will be allowed, as there is no evidence that any medication can increase the risk of adverse effects during tDCS.) Subject is currently enrolled in another investigational device or drug trial(s), or subject has received other investigational agent(s) within 28 days of baseline visit Any condition judged by the patient's physician to cause this clinical trial to be detrimental to the patient