Phase 4 Osteoporosis Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who live independently in their own home or community (not in a care facility)
- People with a body mass index (BMI) over 30, or a BMI between 25 and 30 with at least one additional health risk factor (confirm with trial site for what counts as a risk factor)
- People who currently receive regular (at least annual) dental check-ups
- People who have been found to have lower-than-normal bone density — not quite osteoporosis, but in the range known as "low bone mass" — based on a bone density scan of the hip or spine
Who may not be able to join:
- People who weigh more than 450 pounds (due to limits of the bone density scanning equipment)
- People who live in the same household as someone already taking part in the BEACON study
- People who rely on a quad cane or walker and cannot walk independently
- People who have a history of mild cognitive impairment or dementia, or who score below a certain threshold on a memory and thinking assessment
- People who have consumed more than 21 alcoholic drinks per week in the past month, or who have used any illegal drugs other than cannabis
- People whose weight has changed by 5% or more in the past 3 months
- People who have already been doing structured strength training for more than 60 minutes a day, more than 3 days a week, for over 6 months
- People with severe arthritis, an unhealed fracture, chronic injury, or another condition affecting muscles or joints that would make exercise unsafe; or who have had joint replacement or other bone/joint surgery in the past 6 months or have it planned in the next 12 months; or who have had an invasive dental procedure (such as a tooth extraction or implant) in the past 6 months or have one planned in the next 12 months
- People who have osteoporosis, are on prescription medication for osteoporosis, have had certain bone fractures after age 40 (not caused by a fall or accident), or whose fracture risk score is 20% or higher (confirm with trial site)
- People with very high blood pressure (systolic above 180 or diastolic above 110 mmHg) that remains high across repeated measurements
- People with poorly controlled type 2 diabetes, significantly reduced kidney function, liver disease or abnormal liver results, anaemia, abnormal calcium levels, uncontrolled thyroid disease, or vitamin D deficiency below a certain level
- People who have had a stroke, heart attack, heart failure hospitalisation, or a heart procedure in the past 6 months; or who have a range of other serious health conditions including certain lung, nerve, digestive, or circulatory conditions; active cancer treatment within the last 12 months (except certain skin cancers); significant vision or hearing loss; bilateral hip replacement; past or planned weight-loss (bariatric) surgery; or any condition suggesting a life expectancy of less than 3 years
- People who regularly use growth hormones, weight-loss medications, oral steroids, or certain diabetes medications (such as insulin, thiazolidinediones, or canagliflozin); people with a known allergy to bisphosphonates; or people with significant prior or recent use of certain bone-related medications including bisphosphonates, zoledronic acid, denosumab, anabolic agents, biotin, or strontium
- People who are unable or unwilling to arrange their own transport to study visits, follow the study protocol (including the possibility of being randomly assigned to a group), or attend all required data collection visits
- People currently participating in another research intervention study; people planning to be away for more than one month at a time during the first 6 months of the study; people unwilling to give informed consent (including consent for the trial site to access personal electronic health records); or people considered unsuitable for any other reason by the research team
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Kristen Beavers, PhD, Wake Forest University Health Sciences
Phone: 336-758-5019
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Change in total hip areal bone mineral density (aBMD)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.