Pre-Workout calcium may boost bone strength in veterans
NCT ID NCT05029128
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether taking calcium before exercise can help bones get stronger from workouts. Exercise normally causes a drop in blood calcium, which may limit bone benefits. Researchers gave 18 Veterans calcium or a placebo before exercise to see if it improved bone-building markers. The goal is to create better exercise and nutrition guidelines to prevent fractures.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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18 people
The number who actually took part.
- Started
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Jan 2023
- Finished
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Dec 2025
- Lead sponsor
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A government agency
The lead sponsor is a US federal agency other than the NIH.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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25 to 75 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Female and male Veterans aged 25 to 45 y and 55 to 75 y will be enrolled. Eligible volunteers will be normally active (e.g., recreational cycling or walking) but will not participate in regular moderate-to-vigorous exercise. Women will be premenopausal with regular menstrual cycles or postmenopausal, defined as absence of menses for at least 12 mo or, in those who underwent a hysterectomy, a serum follicle stimulating hormone (FSH) \>30 mIU/mL. Exclusion Criteria: * Initiation or change in dose in the past 6 months of medications that affect bone metabolism * e.g., osteoporosis medications, thiazide/loop diuretics, systemic glucocorticoids * BMD T-score \<-2.5 at the total hip, femoral neck, or lumbar spine * Impaired renal function, defined as an estimated glomerular filtration rate (eGFR) \<60 mL/min/1.73m2 * Abnormal alkaline phosphatase * Untreated thyroid dysfunction, defined as an ultrasensitive thyroid stimulating hormone (TSH) \<0.5 or \>5.0 mU/L * Serum Ca \<8.5 or \>10.3 mg/dL * Serum 25(OH)D \<20 ng/mL * Uncontrolled hypertension (resting systolic blood pressure (BP) \>150 mmHg or diastolic BP \>90 mmHg) * Type 1 diabetes * Type 2 diabetes if on insulin or sulfonylurea therapy * hemoglobin A1c \>7% * Cardiovascular disease; defined as subjective or objective indicators of ischemic heart disease (e.g., angina, ST segment depression) or serious arrhythmias at rest or during the graded exercise test (GXT) * volunteers who have a positive GXT can be re-considered after follow-up evaluation by a cardiologist * Anemia (hemoglobin \<12.1 g/dL for women, \<14.3 g/dL for men) * Fracture in the past 6 months * Body mass index \>39 kg/m2 * In the event of abnormal eGFR, alkaline phosphatase, TSH, BP, 25(OH)D, or hemoglobin values, volunteers can be reassessed, including after appropriate follow-up evaluation and treatment by their health care provider
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Rocky Mountain Regional VA Medical Center, Aurora, CO
Aurora, Colorado, 80045-7211, United States
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Other studies related to the condition(s) this trial covers.
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