RecruitingNot ApplicableNCT07120997

Prunes Preventing Bone Loss in Perimenopause

A Prevention Strategy for the Indication of Prune Consumption in Perimenopausal Females: Can Prunes Attenuate Bone Loss?


Sponsor

Penn State University

Enrollment

124 participants

Start Date

Dec 11, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

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.


Eligibility

Sex: FEMALEMin Age: 44 YearsMax Age: 55 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Calcium supplement, Prunes, and others for people with perimenopausal bone loss. The study is currently recruiting participants at 1 location. People eligible for this study include women aged 44 Years to 55 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DIETARY_SUPPLEMENTPrunes

Participants randomized to the 50g prune group will consume 6 prunes per day for the duration of the 18-month intervention.

DIETARY_SUPPLEMENTCalcium supplement

All participants will consume calcium supplements daily for a baseline period and for the duration of the 18-month intervention.

DIETARY_SUPPLEMENTVitamin D Supplement

All participants will consume Vitamin D supplements daily for a baseline period and for the duration of the 18-month intervention.


Locations(1)

Women's Health and Exercise Laboratory, The Pennsylvania State University

University Park, Pennsylvania, United States

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NCT07120997