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Women in Steady Exercise Research [Formerly Women, Oxidative Stress, Exercise and Estrogens (WOSEE)]

Women in Steady Exercise Research (WISER)

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00393172
Acronym
WISER
Enrollment
400
Registered
2006-10-26
Start date
2006-05-31
Completion date
2010-03-31
Last updated
2019-11-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer, Obesity

Keywords

exercise, breast cancer, prevention, obesity, estrogen metabolism, oxidative stress, IGF-1

Brief summary

RATIONALE: Exercising regularly may lower the risk of breast cancer. PURPOSE: This randomized clinical trial is studying how well exercise prevents breast cancer in healthy young women.

Detailed description

OBJECTIVES: Primary * Compare the changes in urine levels of a stable marker of oxidative stress (F\_2-isoprostanes) in healthy young women who undergo exercise training during 4 menstrual cycles vs no exercise. Secondary * Assess the changes in other metabolic factors that explain the association between physical activity and breast cancer, including: Estrogen metabolism (estrone, estradiol, estriol, 2-OHE\_1, 2-OHE\_2, 2-MeOHE\_1, 2-MeOHE\_2, 4-OHE\_1, 4-OHE\_2 \[as well as ratios of these metabolites\], insulin-like growth factor (IGF)-1 (as well as IGF-binding proteins-1, -2, and -3, insulin, glucose, body composition (including body mass index, lean mass, and body fat \[DEXA scan\]). OUTLINE: This is a randomized, controlled study. Participants are stratified according to baseline body fat percentage and age (18 to 24 years vs 25 to 30 years). Participants are randomized to 1 of 2 intervention arms. * Arm I: Participants exercise for 30 minutes 5 times a week. The intensity of exercise is increased every 4 weeks. The exercise regimen continues for up to 4 menstrual cycles. * Arm II: Participants are observed for 4 menstrual cycles. Participants in both arms undergo 24-hour collection of urine on days 7, 8, and 9 of menstrual cycles 1 and 6. F\_2-isoprostanes are measured via gas chromatography-mass spectrometry (GC/MS). Estrogens are also measured by GC/MS and include E\_1, E\_2, E\_3, 2-OHE\_1, 2-OHE\_2, 4-OHE\_1, 4-OHE\_2, 2-MeE\_1, 2-MeE\_2, 4-MeE\_1, 4-MeE\_2, and 16OHE\_1. Participants undergo blood collection, body mass measurement by dual-energy x-ray absorptiometry, and a fitness assessment twice during the 6-month study. PROJECTED ACCRUAL: A total of 400 participants will be accrued.

Interventions

BEHAVIORALexercise

5 days per week exercise for 4 months

Sponsors

National Cancer Institute (NCI)
CollaboratorNIH
University of Minnesota
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy women * Self-reported menstrual cycle length of 25-35 days within the past 2 months * Nonsmoker * Sedentary (exercise \< 3 times weekly within the past 6 months) * Intact ovaries and uterus * No history of gynecological problems (e.g., fibroids, endometriosis, polycystic ovary syndrome) * Female * Premenopausal * Body mass index 18.5 to 40 * Stable weight (no changes ≥ 10% within the past year)

Exclusion criteria

* No pregnancy or breast feeding within the past 6 months * No plans to become pregnant during study treatment * No cancer within the past 5 years except for nonmelanoma skin cancers * No medical condition that would prohibit participation in a vigorous program of weight-bearing aerobic exercise including, but not limited to, any of the following: * Fibromyalgia * Chronic fatigue syndrome * Metabolic disorders * Recent cardiovascular event * Orthopedic limitations * Psychiatric disorders requiring antipsychotic drugs * No uncontrolled hypertension (systolic blood pressure \[BP\] \> 160 mm Hg and/or diastolic BP \> 99 mm Hg) * No more than 7 alcoholic beverages per week * No injected hormonal contraceptive use within the past year * More than 6 months since prior use of intrauterine device * More than 3 months since prior oral or patch hormone contraceptives * No medication that would prohibit participation in a vigorous program of weight-bearing aerobic exercise

Design outcomes

Primary

MeasureTime frame
Changes in urine levels of F2-isoprostanesBefore and after study

Secondary

MeasureTime frame
Changes in levels of IGF-axis proteinsBefore and after study
Changes in insulin and glucoseBefore and after study
Changes in estrogen metabolitesBefore and after study
Changes in body compositionBefore and after study

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 15, 2026