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NCT07837817
The Impact of a Daily Dietary Supplement on Glycemic Control in Individuals With Overweight or Obesity
Conditions: Glycemic Control, Appetite Regulation
Sex: All
Ages: 18 Years – 65 Years
Healthy volunteers: No
Phase: NA
Enrollment: 60
Sponsor: University of South Alabama
Summary
This clinical trial will evaluate the efficacy of Metabolic Master Pack over a 90-day intervention period. Sixty adults will be randomized to receive either Metabolic Master Pack or placebo. Participants will wear continuous glucose monitors throughout the study, complete repeated blood collections, undergo DEXA body composition assessments, and complete dietary records. Results will provide high-quality evidence regarding the product's effects on glucose regulation and metabolic health.
Eligibility Criteria
Inclusion Criteria:
* BMI 25-40 kg/m²
* Ability to provide informed consent
Exclusion Criteria:
* Taking medications that impact metabolism
* Report sustained weight loss of \>3% in the past 3 months.
* History of metabolic/bariatric surgery.
* Females who are pregnant, have been pregnant within the past 6 months, or plan to become pregnant during the study period.
* Report a current medical condition or treatment for a medical condition that could affect body weight or contradict engagement in any aspect of the outcome measures or interventions.
* Current congestive heart failure, angina, uncontrolled arrhythmia, symptoms indicative of an increased acute risk for a cardiovascular event, prior myocardial infarction or history of cardiomyopathy, coronary artery bypass grafting or angioplasty, conditions requiring chronic anticoagulation (i.e., recent or recurrent DVT).
* Resting systolic blood pressure of \>160 mmHg or resting diastolic blood pressure of \>100 mmHg. If medicated for blood pressure control, the medication dose needs to be stable for \>6 months.
Source: ClinicalTrials.gov (NCT07837817). StuddyBuddy aggregates publicly available trial information.