Clinical trial · Interventional
Sistas Inspiring Sistas Through Activity and Support
SCCDCN-II: Research Project (Breast Cancer)
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
It is known that diet and physical affect a variety of disease-related endpoints and overall health status in general. The investigators also know that dietary and PA intervention effects are difficult for individuals to maintain. By contrast, the investigators have some evidence that group-based and family-centered, multi-component interventions are more effective in terms of creating large changes in diet-related outcomes. Using a group-randomized, controlled design, the overall goal of this project is to reduce breast cancer-related health disparities in a high-risk community, by achieving these Primary Aims,to conduct a regionally-based community-designed dietary and physical activity behavioral controlled trial among AA women,to test the effectiveness of the community-designed, family-based dietary and physical activity behavioral intervention on modifying biomarkers of inflammation and to test the effectiveness of the community-designed, family-based dietary and physical activity behavioral intervention on decreasing breast density
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Prevention Harmful Effects | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Lifestyle | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Lifestyle
- description
- Diet and physical activity intervention group. Measurements taken at baseline, 12 weeks and 1 year.
- interventionNames
- Behavioral: Lifestyle
- type
- NO_INTERVENTION
- label
- Wait-list control
- description
- No-treatment control group. Measurements taken at baseline, 12 weeks and 1 year. People in the control condition can elect to take the intervention after 1 year.
Primary outcomes (1)
- measure
- Inflammatory Response
- timeFrame
- Baseline, 12 weeks and 12 months
- description
- This will entail examining changes in the inflammatory index derived from dietary self-report and self-reported physical activity and blood samples.
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 30 Years
- Maximum age
- 90 Years
Show eligibility criteria text
Inclusion Criteria: * 30 years of age or older * African American * BMI 30 or\< * Willing to be randomized, Exclusion Criteria: * History of cancer * Inflammatory-related conditions * Unstable hormones replacement treatment
References
Publications (0)
Data not yet available