The Bone, Exercise, Alendronate, and Caloric Restriction (BEACON) Trial

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Description

The purpose of this research study is to identify strategies that minimize bone loss that occurs when older adults lose weight. Your participation in this research study will involve a groupmediated weight loss intervention and may involve resistance training and/or 70 mg of weekly oral alendronate or placebo for 52 weeks. Alendronate is a medication that prevents bone breakdown and has been approved by the US Food and Drug Administration (FDA) for the prevention and treatment of osteoporosis in older men and women. In this study, a drug will be compared to a placebo. A placebo is a substance is a substance that is not thought to have any effect on your disease or condition. In this study you will either receive the active study medication, or placebo which is not active. Placebos are used in research studies to see if the drug being studied really does have an effect.

Details
Age

Adult

Type of Study

Outcomes Research

Locations

Outpatient CTRC

Principal Investigator
Photograph of Sarah Wherry,  PhD

Sarah Wherry, PhD

Study ID

Protocol Number: 22-2041

More information available at ClinicalTrials.gov: NCT05764733

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