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Questionnaire Administration / Cancer Prevention / Premenopausal · Interventional Study
ClinicalTrials.gov · August 11, 2026
Early or partial results. Treat as a signal, not a conclusion.
This is a registry record for an active, single-arm lifestyle intervention study designed to assess feasibility (consent, compliance, retention) in premenopausal women at risk for breast cancer. No clinical outcomes or efficacy data are yet reported; the study measures operational endpoints only.
Interventional, Randomized, Parallel, Open label, Prevention purpose. Premenopausal; Female; age from 18 Years; accepts healthy volunteers. Intervention: Group I (IO prevention program). Compared with: Group II (no intervention) — Active Comparator. n = 60. 1 site: United States.
Planned enrollment: 60 participants (estimated) Primary outcomes: consent rate, treatment group compliance rate, and retention rate, each assessed up to 1 year Intervention includes dietary recommendations, physical activity, stress management, mindfulness training, sleep hygiene techniques, and behavioral counseling with social support
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
This registry record does not report any clinical outcomes or efficacy results. Until the study completes and reports its primary feasibility endpoints and any secondary outcomes on breast cancer prevention or biomarkers, clinicians cannot assess whether comprehensive lifestyle change reduces breast cancer risk.
This is a registry record for an active interventional study with feasibility/implementation endpoints (consent, compliance, retention rates) rather than clinical outcomes; no results are reported.
As stated by the source record.
Quoted from the source exactly as published.
This registry record does not report any clinical outcomes or efficacy results. Until the study completes and reports its primary feasibility endpoints and any secondary outcomes on breast cancer prevention or biomarkers, clinicians cannot assess whether comprehensive lifestyle change reduces breast cancer risk.
Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
Registry record from ClinicalTrials.gov (NCT03448003). This is a study registration, not published results. Lead sponsor: M.D. Anderson Cancer Center. Recruitment status: ACTIVE_NOT_RECRUITING. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 60 participants (ESTIMATED). Conditions: Premenopausal. Interventions: OTHER: Cancer Prevention; OTHER: Questionnaire Administration. Primary outcome measures: Consent rate , Up to 1 year; Treatment group compliance rate , Up to 1 year; Retention rate , Up to 1 year. Brief summary: This trial studies how well comprehensive lifestyle change works in preventing patients from breast cancer. A program including dietary recommendations, physical activity, stress management and mindfulness training, learning sleep hygiene techniques, and behavioral counseling in addition to social support may help patients who may be at risk for breast cancer.
Taken from the source record, never inferred. Follow any of these and new work involving them reaches your briefing.