Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03008785
Other study ID # CAAE: 40622414.9.0000.5152
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 2015
Est. completion date December 2016

Study information

Verified date February 2019
Source Federal University of Uberlandia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study evaluate if 10 weeks of mixed exercise combined with isoflavones could have greater effects on climacteric symptoms, body composition and hydratation, lipidic and inflamatory profile than exercise alone in postmenopausal women. the participants will be randomly assigned to the group: placebo and exercise or 100mg of isoflavone and exercise.


Description:

Several endocrine metabolic changes occur during the climacteric period, due to the lack of estrogen and also by the aging process and some studies show that ingestion of isoflavones by postmenopausal women may have benefits. Theoretically the isoflavone potentiate the effects obtained during exercise


Recruitment information / eligibility

Status Completed
Enrollment 32
Est. completion date December 2016
Est. primary completion date July 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 50 Years to 70 Years
Eligibility Inclusion Criteria:

- Healthy postmenopausal woman

- to be able to practice exercises on treadmill and weight exercises

- without physical complications that prevent the execution of physical exercises

- have no history of cardiovascular disease, diabetes, renal pathologies or hypertension

Exclusion Criteria:

- smokers

- use hormone therapy or isoflavone

- use drugs that interfere with lipid and antihypertensive metabolism

Study Design


Related Conditions & MeSH terms


Intervention

Other:
exercise
The training program consisted of aerobic and resisted combined physical exercises performed during 10 weeks, three times weekly with 45 minutes sessions: 5 minutes of warm-up on treadmill, 20 minutes of aerobic exercises and 20 minutes of resistance exercises.
isoflavone
Daily supplementation in 1 capsule per day of 100mg of isoflavones (containing 3.3% genistein, 93.5% dadzein and 3.2% glycitein).
Placebo
Daily supplementation in 1 capsule per day containing starch of corn.

Locations

Country Name City State
Brazil Guilherme Morais Puga Uberlandia Minas Gerais

Sponsors (1)

Lead Sponsor Collaborator
Federal University of Uberlandia

Country where clinical trial is conducted

Brazil, 

References & Publications (2)

Acharjee S, Zhou JR, Elajami TK, Welty FK. Effect of soy nuts and equol status on blood pressure, lipids and inflammation in postmenopausal women stratified by metabolic syndrome status. Metabolism. 2015 Feb;64(2):236-43. doi: 10.1016/j.metabol.2014.09.005. Epub 2014 Oct 5. — View Citation

Lebon J, Riesco E, Tessier D, Dionne IJ. Additive effects of isoflavones and exercise training on inflammatory cytokines and body composition in overweight and obese postmenopausal women: a randomized controlled trial. Menopause. 2014 Aug;21(8):869-75. do — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Change in blood pressure Evaluate change in blood pressure through ambulatory 24-hour blood pressure monitoring used before the begin of intervention and after 10 weeks. Change in blood pressure in 10 weeks intervention
Secondary Climateric Symptoms (Kupperman-Blatt Index) Evaluate the intensity of climateric symptoms using the Kupperman-Blatt Index questionnaire. Consists of 11 questions in which the symptoms are given numerical values according to their intensity . before and after 10 weeks
Secondary Climateric Symptoms (Cervantes Scale) Evaluate the intensity of climateric symptoms using the Cervantes Scale questionnaire. Composed of 31 questions distributed in four domains and 6 possibilities of answer. before the begin the intervention and after 10 weeks
Secondary Climateric Symptoms (Menopause Rating Scale) Evaluate the intensity of climateric symptoms using the Menopause Rating Scale questionnaire. Composed of eleven questions, with five possible answers, Symptoms divided into somatovegetative, psychological and urogenital domains may be classified as absent, mild, moderate, severe and very severe. With a general score ranging from 0 to 55 points before and after 10 weeks
Secondary Lipid profile (enzymatic colorimetric method) The concentrations in mg/dL of total cholesterol, triglycerides, HDL cholesterol, LDL cholesterol and uric acid will be made through the enzymatic colorimetric method. The glucose will be analyzed by the enzymatic method and the glycated hemoglobin A1c by the turbidimetry method. before and after 10 weeks
Secondary Human cytokines (Flow Cytometry) Measurement in pg/mL of the production of human cytokines (IL-8, IL-1ß, IL-6, TNF ( tumor necrosis factor), IL-10 and IL-12p70) in serum samples will be performed by the flow cytometry (FACSCantoII BDTM) Human Inflammatory Cytokines Kit "(BD ™ Cytometric Bead Array (CBA), BD Biosciences, San Jose, CA, USA) according to the manufacturer's instructions. before and after 10 weeks
Secondary Antioxidant capacity The total antioxidant capacity will be evaluated in plasma and saliva using the FRAP (Ferric-Absorbing Ability of Plasma) methodology (Benzie and Strain, 1999). before and after 10 weeks
Secondary Total protein The determination of the total salivary and plasma protein will be performed by the Bradfort method (Bradford, 1976) adapted for microplate before and after 10 weeks
Secondary Body Composition Bioelectrical impedance (Biodynamics, model 450c, EUA) will be used to determine absolute and relative extracellular mass and body cell mass. before and after 10 weeks
Secondary Phase Angle Phase angle in degrees (o) was calculated using the equation (Reactance/Resistance)
*(180/?) using a values obtained on bioelectrical impedance (Biodynamics, model 450c, EUA)
before and after 10 weeks
Secondary Oxidative stress (SOD, Catalase and TBARS activity) The enzyme superoxide dismutase (SOD) will be dosed from the auto oxidation capacity of pyrogallol, a process dependent on the superoxide radical (Fernandes et al., 2011). . Catalase activity in saliva will be determined based on the decrease in absorbance of hydrogen peroxide (H2O2) (Aebi, 1984). Thiobarbituric acid reactive substances (TBARS) will be detected by the Yagi method (Yagi, 1998). before and after 10 weeks
See also
  Status Clinical Trial Phase
Completed NCT02038270 - Accuracy of Nexfin® and NIBP to Predict IBP
Completed NCT02997800 - The Effect of Intraoperative Labetalol on Time to Discharge Phase 2
Completed NCT03168126 - Advanced Hemodynamic Monitoring in Free Flap Surgery N/A
Completed NCT01609491 - Phenylephrine Versus Norepinephrine in Ophthalmic Surgery N/A
Suspended NCT02975505 - Pilot to Examine Risk and Feasibility of Remote Management of BP From CKD Through ESRD N/A