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Life sciences · Interventional Study
ClinicalTrials.gov · November 5, 2026
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Interventional Study.
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Registry record from ClinicalTrials.gov (NCT07919392). This is a study registration, not published results. Lead sponsor: Ohio State University. Recruitment status: RECRUITING. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 40 participants (ESTIMATED). Conditions: Postpartum Depression (PPD). Interventions: DIETARY_SUPPLEMENT: Exogenous ketone supplementation; OTHER: Matched placebo beverage; BEHAVIORAL: Group-Mediated Cognitive Behavioral Counseling; BEHAVIORAL: Structured Group Exercise. Primary outcome measures: Change in Edinburgh Postnatal Depression Scale Total Score , Baseline (Week 0) and Week 16. Brief summary: The purpose of this study is to evaluate the feasibility, acceptability, and preliminary efficacy of a 16-week, fully remote, multimodal intervention combining exogenous ketone supplementation (Qitone™) with group-mediated cognitive behavioral (GMCB) counseling with structured exercise for women diagnosed with postpartum depression (PPD). The study aims to determine whether integrating biochemical, behavioral, and physical activity strategies can improve depressive symptoms, metabolic health, and psychosocial functioning during the postpartum period.