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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04167150
Other study ID # CMI2017-2018
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 6, 2017
Est. completion date May 31, 2018

Study information

Verified date November 2019
Source Oklahoma State University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In spite of aggressive approaches to prevent and treat osteoporosis, it remains one of the most costly and debilitating diseases associated with aging. The pursuit of alternative approaches for preventing bone loss has included the investigation of a number of promising plant-based foods that can be incorporated into the diet. This project is an extension of our pre-clinical studies with tart cherry, designed to determine whether the findings from our animal study can be extended to humans. Thus, the purpose of this project is to investigate the dose-dependent effect of tart cherry juice consumption on biomarkers of bone metabolism in women, aged 65-80 years. The hypothesis to be tested is that three months of tart cherry supplementation will improve bone biomarkers in a dose-dependent manner. Moreover, these improvements in bone metabolism will correspond to a decrease in markers of inflammation and oxidative stress.


Description:

Tart cherries are an excellent course of phenolic compounds and anthocyanins, and in pre-clinical studies have been shown to prevent age-related bone loss. Based on these findings, this pilot study was designed to investigate the effects of three months of tart cherry juice supplementation on improving markers of oxidative stress and bone metabolism in older women. Women (n=30), aged 65-80 yrs, will be recruited for the study and randomly assigned to one of two doses of tart cherry juice (8 or 16 fl oz) per day prepared from a Montmorency cherry concentrate (King Orchards, Central Lake, MI). Study participants will complete two study visits to the Nutritional Sciences Clinical Research Center. At the first visit, informed consent will be obtained and relevant medical history and anthropometric measures will be taken by the research team. A blood draw will be performed to assess baseline, biochemical markers of bone metabolism and inflammation as well as indicators of oxidative status. A physical activity and food frequency questionnaire will be completed by each study participant. Whole body, hip and spine bone density (DXA) scan will be performed by certified bone densitometrist. A 3-month final visit will be scheduled for all study participants in which most of the procedures described at baseline (except DXA) will be repeated. Change in primary and secondary outcome measures (i.e., bone, inflammation and oxidative stress biomarkers) will be assessed.


Recruitment information / eligibility

Status Completed
Enrollment 33
Est. completion date May 31, 2018
Est. primary completion date May 31, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 65 Years to 80 Years
Eligibility Inclusion Criteria:

- Women, 65-80 years of age

- Capacity to give informed consent

Exclusion Criteria:

- Hormone replacement therapy in the 3 months prior to starting the study

- Bisphosphonates in the 3 months prior to starting the study

- Raloxifene in the 3 months prior to starting the study

- Intermittent parathyroid hormone in the 3 months prior to starting the study

- Growth hormone or steroids in the 3 months prior to starting the study

- Osteoporosis

- Renal disease

- Cancer

- Cardiovascular disease

- Diabetes

- Respiratory disease

- Gastrointestinal diseases

- Liver disease

- Other chronic conditions that could affect bone metabolism

Study Design


Intervention

Dietary Supplement:
tart cherry juice concentrate is a commercial product provided by King Orchards (Central Lake, MI)
Participants were instructed to reconstitute the tart cherry juice concentrate in 8 fl oz of water and consume either 1x or 2x daily for 3 months.

Locations

Country Name City State
United States Oklahoma State University - Nutritional Sciences Stillwater Oklahoma

Sponsors (2)

Lead Sponsor Collaborator
Oklahoma State University Cherry Marketing Institute Research Committee

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Bone-specific alkaline phosphatase (U/L) Bone formation marker Change from baseline to final visits (3 month intervention)
Primary Tartrate resistant acid phosphatase (U/L) Bone resorption marker Change from baseline to final visits (3 month intervention)
Secondary C-reactive protein (mg/L) Marker of inflammation Change from baseline to final visits (3 month intervention)
Secondary Thiobarbituric acid reactive species (TBARS) (U/L) Marker of oxidative stress Change from baseline to final visits (3 month intervention)
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