Patients who are involved in a clinical protocol driven 12 week medical weight loss intervention will be randomized to receive either a placebo or 600 mg of an ashwagandha root extract. The study endpoints are primarily the patients self-reported perception of life stress and sleep quality. The working hypothesis of this study is that the addition of aschwagandha to .the medical weight loss program will improve the self-reported perception of life stress and sleep quality
During this 12-week medical weight loss program, the randomized patients will also have a baseline measurements and final measurements of blood for selected adipokines , cytokines, and telomerase measurements
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
TRIPLE
Enrollment
35
Participants will take one 300 mg capsule of Ashwagandaha Root Extract orally twice a day for 12 weeks.
Participants will take one placebo capsule orally twice a day for 12 weeks.
Loma Linda University Center for Health Promotion
Loma Linda, California, United States
Perceived Stress Scale PSS
Standardized questionnaire
Time frame: 12 weeks
Pittsburgh Sleep Quality Index PSQI
Standardized questionnaire
Time frame: 12 weeks
Food Craving Questionnaire - Trait FCQ-T
Standardized questionnaire
Time frame: 12 weeks
Three-Factor Eating Questionnaire TFEQ
Standardized questionnaire
Time frame: 12 weeks
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