Osteoporosis Clinical Trial
— MedSDOfficial title:
Mediterranean Diet for Post-menopausal Women: Effects on Bone Turnover
Verified date | May 2017 |
Source | UConn Health |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The investigators propose a 24 week clinical research trial (12 week observational period followed by 12 week MedSD intervention) with feasibility of diet adoption and markers of bone turnover as the primary outcomes.
Status | Completed |
Enrollment | 22 |
Est. completion date | December 2014 |
Est. primary completion date | December 2014 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 65 Years and older |
Eligibility |
Inclusion Criteria: - postmenopausal women > 65 years - BMI<30 kg/m2 - able to travel to clinical sites for follow-up visits - willing to make no changes to habitual physical activity or calcium and vitamin D intake for the study duration Exclusion Criteria: - any disease that may affect bone metabolism, (i.e Paget's disease, primary hyperparathyroidism) - cancers of any kind (except basal or squamous cell of skin) in past 5 years - use of medication known to affect bone metabolism - extreme dietary behaviors or supplementation in excess of DRI upper limits - following a medically prescribed diet or dietary pattern similar to the MedSD - history of chronic renal or liver disease - history of hip fracture or known vertebral fracture within the past year - persons with an allergy to fish or nuts. |
Country | Name | City | State |
---|---|---|---|
United States | UCHC | Farmington | Connecticut |
Lead Sponsor | Collaborator |
---|---|
UConn Health | University of Connecticut |
United States,
Bihuniak JD, Ramos A, Huedo-Medina T, Hutchins-Wiese H, Kerstetter JE, Kenny AM. Adherence to a Mediterranean-Style Diet and Its Influence on Cardiovascular Risk Factors in Postmenopausal Women. J Acad Nutr Diet. 2016 Nov;116(11):1767-1775. doi: 10.1016/j — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | study adherence | Determine the extent to which postmenopausal women in the US can adhere to the MedSD intervention. | 8 months | |
Secondary | Bone turnover markers | Determine if adherence to the MedSD will result in a reduction in bone resorption markers and enhance formation markers | 8 months |
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