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Physical Activity Targeting Metabolic Syndrome for Prevention of Breast Cancer in SAI Women
RECRUITINGN/ASponsored by Rush University Medical Center
Actively Recruiting
PhaseN/A
SponsorRush University Medical Center
Started2025-05-01
Est. completion2026-06-30
Eligibility
Age40 Years – 65 Years
SexFEMALE
Healthy vol.Accepted
Locations2 sites
View on ClinicalTrials.gov →
NCT06827704
Summary
This study aims to to improve physical activity and metabolic outcomes for breast cancer prevention in South Asian Indian immigrant women.
Eligibility
Age: 40 Years – 65 YearsSex: FEMALEHealthy volunteers accepted
Inclusion Criteria: * Self-identified first-generation SAI woman aged 40-65 years without breast cancer diagnosis (permanent residency in US or are in the process of obtaining permanent residency) * Insufficiently active (self-reported \<150 minutes/week of moderate-intensity or \<75 minutes/week of vigorous-intensity PA in the past month) * Conversant in Hindi * Owns a smartphone for Fitbit application * Has a computer or mobile device with Internet access * Willing to participate in recorded Virtual intervention sessions * Medical clearance if has Type 1 diabetes, or Type 2 diabetes with an A1C ≥ 9.0%, or have an A1C of ≥ 6.5% without a prior diabetes diagnosis * Has no disabilities preventing regular PA determined by Physical Activity Readiness Questionnaire (PAR-Q \& You) Exclusion Criteria: * Major signs/symptoms of pulmonary or CVD, unstable cardiac or pulmonary disease in the past month, or other conditions interfering with walking (per PAR-Q \& You) * Systolic BP ≥160 and/or diastolic BP ≥100
Conditions5
Breast CancerBreast Cancer PreventionCancerMetabolic SyndromePhysical Activity
Locations2 sites
Rush University College of Nursing
Chicago, Illinois, 60612
Rush University College of Nursing
Sugar Grove, Illinois, 60554
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Actively Recruiting
PhaseN/A
SponsorRush University Medical Center
Started2025-05-01
Est. completion2026-06-30
Eligibility
Age40 Years – 65 Years
SexFEMALE
Healthy vol.Accepted
Locations2 sites
View on ClinicalTrials.gov →
NCT06827704