- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01120665
Isolated and Associated Effects of Physical Exercise and Estrogen Therapy on Climactercs Women (TRH01/989-7)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
More than an isolated event, menopause is an universal process that produces many physiologic changes, affecting not only the reproductive tissues but other systems of women's body. Post-menopause period is usually accompanied by an increase in climacteric symptoms, which decrease healthy related quality of life. Moreover, many unhealthy changes occur at this period of women's life, increasing the risk for metabolic syndrome development, which might be due, at least in part, to an increase in insulin resistance and compensatory hyperinsulinemia.
Hormone therapy is indicated as the main treatment to reduce or relief the negative effects of menopause. Although many studies have confirmed the possible positive effects of this approach on postmenopausal symptoms, its effects on insulin resistance and other metabolic syndrome factors remain controversial.
On the other hand, it's well known that acute and chronic exercises can provide a wide range of benefits for postmenopausal women's health, including decrease of insulin resistance and symptoms relief.
In clinical practice, many postmenopausal women are using hormone therapy and are instructed to exercise. However, the effects of this association are poorly studied.
Thus, the main goal of this randomized placebo-controlled trial was to evaluate, in healthy, middle age, and hysterectomized postmenopausal women, the single and combined effects of physical exercise and oral estrogen use on blood pressure (BP), heart rate (HR), muscle blood flow, and autonomic function measured at baseline conditions and under hyperinsulinemia stimulus. Moreover, it also investigated the effects of these interventions on symptoms relief and quality of life.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Hysterectomy women, with or without ovaries, confirmed by transvaginal ultrasound.
- Climacteric women, postmenopausal for at least 1 year, with vasomotor symptoms (Kupperman, 1959) and/or laboratory diagnosis of menopause (high luteinizing hormone [LH] and follicle-stimulating hormone [FSH] and estradiol decreased).
Exclusion Criteria:
- Hypertension or other cardiovascular disease (thromboembolism, heart disease, myocardial infarction, stroke, vascular disorders, coronary insufficiency or venous)
- Osteoporosis.
- Diagnose or suspected breast cancer or ovaries.
- Current illness or a history of severe liver failure, jaundice or severe pruritus pregnancy and liver tumor.
- Endocrine and metabolic diseases as diabetes, thyroid disorders, obesity and dyslipidemia.
- Chronic diseases such as kidney diseases and collagen diseases.
- Women with cervical or vaginal malignancies.
- Hypersensitivity to estradiol valerate.
- Previous use of estrogen-containing implants in the last two years, use of hormone replacement therapy (HRT) orally or transdermally in the last three months or HRT use by injection in the last six months before the study start.
- Limited mobility or other physical problems that contraindicate the physical exercises.
- Women who are engaged in regular physical activity.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: PLACEBO-CONTROL
PLACEBO + CONTROL TO EXERCISE
|
lactose powder, corn starch, microcrystalline cellulose, and magnesium stearate
The control group was advised to maintain their normal habits, and not to begin any physical exercise program during the study period
Other Names:
|
|
Experimental: ESTROGEN THERAPY + CONTROL
ESTROGEN THERAPY (estradiol valerate 1 mg/dia orally) + CONTROL TO EXERCISE
|
The control group was advised to maintain their normal habits, and not to begin any physical exercise program during the study period
Other Names:
estradiol valerate, 1 mg/day, orally.
Other Names:
|
|
Experimental: PLACEBO+AEROBIC TRAINING
PLACEBO + AEROBIC TRAINING (cicle-ergometer, 50 minutes, 3x week)
|
lactose powder, corn starch, microcrystalline cellulose, and magnesium stearate
Aerobic trainin (cycleergometer, 3x/week, moderate intensity, 50 minutes)
Other Names:
|
|
Experimental: ESTROGEN THERAPY + AEROBIC TRAINING
ESTROGEN THERAPY (estradiol valerate 1 mg/dia orally) + AEROBIC TRAINING (cicle-ergometer, 50 minutes, 3x week)
|
estradiol valerate, 1 mg/day, orally.
Other Names:
Aerobic trainin (cycleergometer, 3x/week, moderate intensity, 50 minutes)
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Blood pressure
Time Frame: six months
|
Blood pressure will be measured as often as needed, respecting the interval 1-2 minutes among measurements, until you obtain three consecutive measurements with a difference of less than 5 mmHg by auscultation and oscilometric methods.
The verification of calibration of the monitor is often assessed by comparison with the mercury.
|
six months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
hemodynamics mechanisms
Time Frame: six months
|
Hemodynamics mechanisms will be evaluate by air-occlusion pletismography
|
six months
|
|
autonomics mechanisms
Time Frame: six months
|
autonomics mechanisms will be evaluated by microneurography methods and heart rate and blood pressure variability
|
six months
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Angela M Fonseca, PhD, University of Sao Paulo
- Principal Investigator: Decio Mion Jr, PhD, University of Sao Paulo
- Principal Investigator: Cláudia LM Forjaz, PhD, University of Sao Paulo
- Principal Investigator: Sandra B Abrahão, PhD, University of Sao Paulo
- Principal Investigator: Taís Tinucci, PhD, University of Sao Paulo
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- TRH01/989-7
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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