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Symptoms of Polycystic Ovarian Syndrome Ameliorated by Keto-Adaptation Pilot
NCT07227363 · Ohio State University
In plain English
Click the button to translate this study into plain language — what it is, who qualifies, and what participation looks like.
About this study
The SPARK study (Symptoms of PCOS Ameliorated by Responses to Keto-adaptation) is a 12-week randomized, two-arm intervention examining how nutritional ketosis influences ovulatory and metabolic outcomes in women with Polycystic Ovary Syndrome (PCOS).
PCOS is a common endocrine disorder that affects hormone balance, menstrual function, and metabolism. Current treatments often address single symptoms but rarely provide comprehensive improvement. Ketogenic dietary interventions have shown promise for improving insulin sensitivity, hormone profiles, and body composition; however, few studies have evaluated their direct impact on ovulation.
In this pilot trial, 40 women aged 18-40 years with diagnosed PCOS will be randomized to one of two groups:
Ketogenic Diet (KD): Participants will follow a low-carbohydrate, high-fat, moderate-protein diet designed to achieve and maintain nutritional ketosis (β-hydroxybutyrate ≥0.5 mmol/L).
Mixed Diet + Exogenous Ketone Supplement: Participants will consume a balanced diet aligned with USDA macronutrient recommendations and receive a ketone ester supplement.
Primary outcomes include changes in ovulatory status, assessed through hormonal markers, ovulation prediction tests, and continuous basal body temperature monitoring (OvuSense). Secondary outcomes include changes in reproductive hormones (progesterone, estrogen, LH, FSH), metabolic and lipid markers, and exploratory imaging of cardiovascular function and ovarian morphology via MRI.
This study will provide feasibility and preliminary efficacy data to inform a future large-scale clinical trial evaluating ketogenic strategies for improving menstrual regularity and overall health in women with PCOS.
Eligibility criteria
Inclusion Criteria:
* Female participants aged 18-40 years.
* Clinical diagnosis of Polycystic Ovary Syndrome (PCOS) according to Rotterdam criteria (presence of at least two of the following: oligo- or anovulation, clinical or biochemical signs of hyperandrogenism, and/or polycystic ovaries on ultrasound).
* Willingness and ability to comply with all study procedures, including fasting (\>10 hours; water only), avoidance of alcohol (\>24 hours), and abstaining from exercise (\>24 hours) prior to each test visit.
* Willing to maintain current diet, exercise, medication, and supplement habits throughout the study.
* Body mass index (BMI) ≥18 kg/m².
* Access to a smartphone, computer, or tablet for digital tracking and study communication.
Exclusion Criteria:
* Current adherence to a low-carbohydrate diet (\<30% of total energy from carbohydrates).
* Non-PCOS etiologies of anovulation (e.g., menopause, oophorectomy, or other reproductive disorders).
* History of type 1 diabetes or uncontrolled type 2 diabetes.
* Weight loss ≥10% of body weight within the previous 6 months.
* Pregnancy or breastfeeding.
* Use of hormonal contraception or medications known to alter reproductive hormones within 3 months prior to enrollment.
* Active eating disorder or medical condition that could interfere with dietary intervention.
* Any condition that, in the opinion of the Investigator, could interfere with participation, data integrity, or safety.
Study design
Enrollment target: 40 participants
Allocation: randomized
Masking: none
Age groups: adult
Timeline
Starts: 2025-02-01
Estimated completion: 2026-12
Last updated: 2025-11-12
Interventions
Other: Ketogenic dietDietary Supplement: Exogenous Ketone Supplement
Primary outcomes
- • Change in Ovulatory Status (Baseline to 12 weeks)
Sponsor
Ohio State University · other
Contacts & investigators
ContactMadison Kackley, PhD · contact · Kackley.19@osu.edu · 16142479650
InvestigatorMadison Kackley, PhD · principal_investigator, Ohio State University
All locations (1)
The Ohio State UniversityRecruiting
Columbus, Ohio, United States