Impact of Reducose® on Glycemic Response and Menopausal Symptoms in Perimenopausal Women (CALM-R)
Purpose
The purpose of this double-blind, randomized, placebo-controlled trial is to. evaluate daily Reducose® (mulberry leaf extract) supplementation taken with the two largest meals for 12 weeks on improving glycemic response and perimenopausal symptoms in women aged 40-60 years. Glycemic response is measured using Dexcom Stelo continuous glucose monitors during standardized test meals, and menopausal symptoms and sleep/quality-of-life outcomes are assessed using validated surveys administered through the Chloe app in a decentralized U.S. study.
Conditions
- Glycemic Response
- Menopause Symptoms
Eligibility
- Eligible Ages
- Between 40 Years and 60 Years
- Eligible Sex
- Female
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- Participants assigned female at birth (aged 40-60 years) will be recruited for the study. - Females ages 40-60 who are weight stable and with a self- reported Body Mass Index (BMI) between 18.5 to 35 kg/m2. - Willing to maintain their existing dietary and physical activity patterns throughout the study period. - Have received a medical physical screening (annual physical) within the last 12 months where blood markers for diabetes were taken and results were within the healthy range. - Self-reported >40yrs in age and experiencing irregular periods. - Willing and able to comply with the study protocol. - Has given voluntary informed consent to participate in the study. - Not currently using hormone replacement therapy (HRT) and/or >3months since their last hormone treatment. - Experiencing menopause symptoms and meets the minimum score of 12/60 on the Greene Climacteric Scale (GCS). - Own or have constant access to a smart phone and the apple or android app stores and are willing and able to download the Dexcom and Chloe apps and accept their respective privacy policies. - Willing to practice a reliable method of non-hormonal contraception for the duration of the study. - In good general health at the time of screening (Investigator discretion). - Able to read, understand, and provide informed consent in English. - Able to receive shipment of the product at an address within the United States. - Able to complete study assessments over the course of up to 12 weeks.
Exclusion Criteria
- Participants assigned male at birth. - Aged > 60 or < 40 years. - Pregnant or lactating. - Body mass index (BMI) > 35kg/m2 or < 18.5kg/m2 - Fasting blood glucose >126mg/dL and/or HbA1c >6.5% reported in routine medical physical screening within the last 12-months. - Known history of diabetes mellitus (Type I/II) or the use of antihyperglycemic drugs or insulin to treat diabetes and related conditions. - Currently using hormone replacement therapy (HRT) or had hormone therapy in the last 3 months. - Postmenopausal, experiencing amenorrhea for >12months. - Underwent medically induced or surgical menopause. - History of hysterectomy or full or partial oophorectomy. - Any known food allergy or intolerance including mulberry extract. - Medical condition(s) or medication(s) known to affect glucose regulation or appetite and/or influence digestion and absorption of nutrients, including thyroid conditions, active inflammatory bowel disease (Crohn's disease or ulcerative colitis) and incretin mimetics (GLP-1, Semaglutide, Dulagluetide, Tirzepatide, etc.) - Previously undergone bariatric surgery. - Use steroids, protease inhibitors, antipsychotics, antidepressants (including selective serotonin reuptake inhibitors and monoamine oxidase inhibitors) (all of which have effects on glucose metabolism and body fat distribution). - Significant or untreated medical and/or psychiatric disorders including but not limited myocardial ischemia or infarction, unstable angina, uncontrolled hypertension, renal failure and serious renal diseases, undergoing dialysis, chronic active hepatitis, acute hepatitis, cirrhosis of liver, AIDS, malignancy or neurological disorders including epilepsy, recent cerebrovascular disease or recent traumatic brain injury. - Alcohol intake above recommendations (>2 standard alcoholic drinks per day) or drug abuse or dependence within the past 6 months. - Currently smoke tobacco and cannabis products (including vaping). - Consuming extremely restrictive diet currently or within past 3 months. - Weight has varied significantly (+/- 5 lbs) in the past 3 months. - Cognitively impaired and/or who are unable to give informed consent. - Taking daily medications or dietary supplements that have a significant effect on blood glucose control either as a primary function or side effect. - Subject to a major medical, surgical or major depressive or psychiatric event requiring hospitalization within the preceding 3 months. - Use of over the counter medications like Herbal Supplements: Black Cohosh, Dong Quai, Maca Root, Red Clover, Chaste Tree Berry (Vitex), Soy Isoflavones, Ashwagandha; OTC Non-Herbal Supplements: DHEA, Progesterone Cream (Bioidentical), Melatonin. - Participation in any other clinical research trial within 30 days prior to randomization. - Do not have a personal smartphone, internet access, or unwilling to download Chloe or use a Dexcom Continuous Glucose Monitoring Device. - Are unlikely for any reason to be able to comply with the study protocol, do not provide informed consent, or considered unsuited for participation in the study by the Principal Investigator.
Study Design
- Phase
- N/A
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel Assignment
- Intervention Model Description
- Parallel Assignment (two-arm RCT)
- Primary Purpose
- Treatment
- Masking
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
- Masking Description
- This study is a randomized, double-blind, placebo-controlled trial. Participants, care providers, investigators, and outcomes assessors are blinded to intervention assignment. Study products are labeled as Product A or Product B, and the randomization code is maintained by the sponsor and only broken in the event of a serious adverse event.
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Experimental Reducose® Mulberry Leaf Extract |
|
|
|
Placebo Comparator Matching Placebo |
|
Recruiting Locations
People Science
Los Angeles 5368361, California 5332921 90034
Los Angeles 5368361, California 5332921 90034
More Details
- NCT ID
- NCT07333885
- Status
- Recruiting
- Sponsor
- Phynova Group Ltd