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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01476033
Other study ID # 23-508 ex 10/11
Secondary ID
Status Completed
Phase N/A
First received November 16, 2011
Last updated April 9, 2013
Start date October 2011
Est. completion date December 2012

Study information

Verified date April 2013
Source Green Beat
Contact n/a
Is FDA regulated No
Health authority Austria: Ethikkommission
Study type Interventional

Clinical Trial Summary

The investigators investigate the impact of an encapsulated fruit, berry and vegetable juice powder concentrate on oxidative stress, inflammation and blood flow before and post exercise in overweight, middle-aged, women.

Main hypotheses (H1):

- The nutraceutical has an impact on oxidative stress reduction.

- The nutraceutical has an impact on inflammation.

- The nutraceutical has an impact on blood flow and microcirculation.

- Walking exercise for 30 minutes has an impact on oxidative stress- and inflammation markers.

- Walking exercise for 30 minutes has an impact on blood flow and microcirculation

- The combination of nutraceutical supplementation + walking exercise for 30 minutes has an impact on oxidative stress- and inflammation markers, and on blood flow/microcirculation.


Recruitment information / eligibility

Status Completed
Enrollment 44
Est. completion date December 2012
Est. primary completion date April 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 35 Years to 50 Years
Eligibility Inclusion Criteria:

- women

- BMI > 27

- praemenopausal

- non smokers

- eligibility for exercise

- 4wk wash out

Exclusion Criteria:

- male

- all people not matching this age group

- BMI > 40 and < 27

- peri- or postmenopausal women

- smokers

- all women taking dietary supplements

- all women that fail in ergometric exercise eligibility testing, refering to the standards in sports medicine (e.g.: significant ST-decrease or increase, blood pressure > 240 mmHg, tachycardia, polymorphic extrasystolia, cyanosis, bradyarrhythmia..)

- Diabetics

- osteoporosis or osteopenia

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
nutraceutical group
6 capsules of supplement or placebo for 8wk

Locations

Country Name City State
Austria Medical University of Graz Graz

Sponsors (1)

Lead Sponsor Collaborator
Green Beat

Country where clinical trial is conducted

Austria, 

Outcome

Type Measure Description Time frame Safety issue
Primary Carbonyl groups on protein, oxidized LDL, Malondialdehyde, TNF-alpha, IL-6, Trombelastometry and peripheral microcirculation Carbonyl groups on protein as indicators of protein oxidation; oxidized LDL, Malondialdehyde as indicators of Lipidoxidation; TNF-alpha, IL-6 as indicators of inflammation; Trombelastometry: clotting time, thrombocyte ahesion, trombocyte aggregation from whole blood as indicators for blood flow and hemostasis; Peripheral microcirculation in subcutis as indicator for blood flow in peripheral subcutis. 6 months No
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