Phase 2
Completed N=40
Research Investigation of Soy and Estrogen
Menopause · Hot Flashes
Source: ClinicalTrials.gov NCT00997893 ↗
Enrolled (actual)
40
Serious AEs
0.0%
Results posted
Dec 2020
Primary outcomePrimary: Change in STAI-6 Score — 12.31; 11.85; 10.76; 11.69 score on STAI scale — p=.004
Summary
The purpose of this study is to determine the effects of oral estradiol and soy phytoestrogens on anxiety, stress responsivity and cognition in perimenopausal women.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Change in STAI-6 Score |
12.31; 11.85; 10.76; 11.69; 11.38; 11.24 | .004 sig |
| PRIMARY Changes in STAI-6 Scores Before and After Psychosocial Stressor Over Time |
8.73; 8.69; 9.77; 12.61; 12.92; 12.23 | .98 |
| PRIMARY Memory for Emotionally Valent Words and Neutral Words |
0.45; 0.45; 0.38; 0.48; 0.40; 0.47 | .68 |
| PRIMARY Change in Verbal Memory, Immediate Recall |
-.02; 2.31; 2.08 | .11 |
| PRIMARY Change in Verbal Memory, Delayed Recall |
.87; 1.61; 1.08 | .86 |
Eligibility Criteria
Inclusion Criteria
- Female
- Perimenopausal as defined by the Stages of Reproductive Aging Workshop (STRAW) criteria, specifically in either of the two following stages: a) early transition defined as changes in cycle length of seven days or more in either direction in consecutive cycles or b) late transition defined as > 60 days amenorrhea and FSH > 40 IU/mL
- Intact uterus/ovaries (i.e. no surgical menopause)
- at least 1 self-reported hot flash per week
- Estrogen therapy not contraindicated
- Able to give informed consent
- Age between 40 and 65 years
- English as first and primary language
Exclusion Criteria
- Positive pregnancy test or breastfeeding (pregnancy tests will be given to all women)
- Obesity > 35 BMI
- Previous history of endometrial hyperplasia/neoplasia
- Previous history of cancers of the breast or reproductive tract
- History of presence of myocardial infarction (MI) or stroke
- Current clinical diagnosis or a diagnosis within the past year of an anxiety disorder, severe recurrent depression, or severe psychiatric disturbance
- History of head injury with more than 60 minutes loss of consciousness
- History of neurological condition affecting cognitive function (e.g., brain tumor, multiple sclerosis)
- History of developmental disability affecting cognitive function (e.g., mental retardation, attention deficit)
- Current use of CNS-acting medication (e.g., antidepressants, anxiolytics, diphenhydramine)
- History or presence of cerebrovascular accident, sickle cell anemia
- History of alcohol or drug abuse as defined by DSM criteria
- Abnormal vaginal bleeding of undetermined cause
- Untreated or uncontrolled hypertension defined as systolic blood pressure greater than 165 mm hg or diastolic blood pressure greater than 95 mm hg
- Concurrent administration of medication containing estrogen, progestin, SERM within four months of enrollment
- Concurrent administration of medication containing St. John's wort, bisphosphonates, or dietary phytoestrogens within one month of enrollment
- History of migraine associated with hormone use
- History or presence of deep vein thrombosis, thrombophlebitis or thromboembolic disorder
- Current participation in any other clinical trial within 30 days of enrollment
- Smoker
- Diabetes
- Premature ovarian failure (defined as having last menstrual period before age 40)
- Abnormal PAP smear in previous year
- Abnormal mammogram in previous year
- Vegans (vegetarians who tend to consume greater than average doses of phytoestrogens)
- Allergy to soy (affects ~1% of people in the United States; reactions are typically mild)
- Symptomatic fibroids (significant size or significant menstrual changes)
- Menorrhagia
- Lactose intolerant
Data sourced from ClinicalTrials.gov (NCT00997893). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.