A Study of High-Dose Vit D Versus Standard of Care Vit D Supplementation
- Conditions
- Breast CancerOsteoporosisBreast
- Interventions
- Dietary Supplement: High Dose Vitamin DDietary Supplement: Standard of Care Vitamin D
- Registration Number
- NCT05016310
- Lead Sponsor
- Wake Forest University Health Sciences
- Brief Summary
This is a randomized study evaluating the effects of early intensive vitamin D supplementation compared to standard of care vitamin D supplementation on bone health over an 18 month period.
- Detailed Description
This is a randomized, open-label study designed to evaluate the effect of high dose vitamin D versus standard of care vitamin D supplementation on bone health and arthralgias. The randomization will be stratified by hormone receptor status (positive versus negative). The primary objective is to compare the effect of high dose vitamin D to the current standard vitamin D treatment administration algorithm on bone health, as measured by percent change from baseline in bone mineral density (g/cm2), in young women with non-metastatic breast cancer who receive systemic therapy.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 7
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description High Vit D High Dose Vitamin D High Dose Vitamin D SOC Vit D Standard of Care Vitamin D Standard of Care Vitamin D
- Primary Outcome Measures
Name Time Method Percent change from baseline in bone mineral density (g/cm^2) from baseline to the Year 1 DEXA scan 15 months (12 plus a +3 month calendar window) Compare effect of high dose vitamin D to the current standard vitamin D treatment administration algorithm on bone health, as measured by percent change from baseline in bone mineral density (g/cm2) to the Year 1 planned DEXA scan, in young women with non-metastatic breast cancer who receive systemic therapy.
- Secondary Outcome Measures
Name Time Method 25(OH) D level over time 18 months Compare effect of high dose vitamin D to the current standard vitamin D treatment administration algorithm 25(OH) D levels in young women with non-metastatic breast cancer who receive systemic therapy.
PRAI questionnaire results over time 18 months Compare effect of high dose vitamin D to the current standard vitamin D treatment administration algorithm on PRAI questionnaire results in young women with non-metastatic breast cancer who receive systemic therapy.
Skeletal complications over time 18 months Compare effect of high dose vitamin D to the current standard vitamin D treatment administration algorithm on skeletal complications in young women with non-metastatic breast cancer who receive systemic therapy.
Overall satisfaction with pain control over time 18 months Compare effect of high dose vitamin D to the current standard vitamin D treatment administration algorithm on overall satisfaction with pain control in young women with non-metastatic breast cancer who receive systemic therapy.
Trial Locations
- Locations (1)
Levine Cancer Institute
🇺🇸Charlotte, North Carolina, United States