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Study identifier: NCT07120997 Synced from ClinicalTrials.gov · July 28, 2026
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Prunes Preventing Bone Loss in Perimenopause

Condition: Perimenopausal Bone Loss  ·  Sponsor: Penn State University

PhaseNA
Planned participants124
Who can joinFemale, 44 Years to 55 Years
Healthy volunteersYes

About this study

Dietary interventions of prune consumption during the transmenopausal period are innovative methods to prevent bone loss. Modern medicine does not intervene to prevent or attenuate this highly vulnerable period of bone loss which, if successfully attenuated, can potentially prevent/delay osteoporosis in women. The transmenopausal period represents an opportunistic window for the study because bone loss is at its greatest at this time, with females losing as much as 6-7% of bone. If this project is successful at attenuating bone loss, it can immediately be disseminated to the public to promote prune consumption to slow down and attenuate perimenopausal bone loss. As such, this project could improve the long-term bone health of females and avoid or delay osteoporosis and improve quality of life. The long-term goal of this study is to test the novel hypothesis that prune consumption for 18 months during the 3-year transmenopausal period prevents the dramatic rate of bone loss in perimenopausal females during a window of heightened physiological vulnerability. At Penn State University, the study will compare the effects of 18 months of daily dietary consumption of 50 g of prunes (5-6) versus a no-prune control group on bone outcomes (bone mineral density, bone geometry), mechanistic factors (bone and inflammatory markers, inflammatory response of ex vivo cultured peripheral blood mononuclear cells, monocytes), and gut microbiome.

This description comes directly from the study's public registry record.

Talk to the study team

Mary Jane De Souza, PhD  ·  814-863-0045  ·  mjd34@psu.edu

Nancy I. Williams, ScD  ·  814-865-1346  ·  niw1@psu.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Women's Health and Exercise Laboratory, The Pennsylvania State UniversityUniversity Park, Pennsylvania, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07120997