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Cognitive Behavioral Therapy as an Intervention to Prevent Weight Rebound post Semaglutide Discontinuatio

Not Applicable
Conditions
Obesity
Registration Number
JPRN-UMIN000053018
Lead Sponsor
kansai medical university
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
40
Inclusion Criteria

Not provided

Exclusion Criteria

Patients who fall under any of the following will not be included in this study. 1) Patients with severe hepatic or renal dysfunction 2) Pregnant and lactating women 3) Patients with malignant tumor 4) Patients with severe heart failure/arrhythmia 5) Patients with secondary obesity due to endocrine (hormone) or other drugs, etc. 6) Patients with a history of hypersensitivity to semaglutide 7) Patients with diabetic ketoacidosis, diabetic coma or precoma, type 1 diabetes 8) Severe infections in patients with type 2 diabetes, conditions requiring emergency surgery, etc. 9) Other patients deemed unsuitable as research subjects by the research director

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Weight change rate from discontinuation of semaglutide to 24 weeks after discontinuation
Secondary Outcome Measures
NameTimeMethod
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