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Life sciences · Interventional Study
ClinicalTrials.gov · October 6, 2026
No summary has been generated for this record yet. What follows is drawn from its source metadata only.
Interventional Study.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
The source did not state who this applies to in practice.
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Registry record from ClinicalTrials.gov (NCT03546972). 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: 51 participants (ACTUAL). Conditions: Deleterious BRCA1 Gene Mutation, Deleterious BRCA2 Gene Mutation, Ductal Breast Carcinoma In Situ, Obesity, Overweight, Premalignant Lesion. Interventions: OTHER: Behavioral, Psychological or Informational Intervention; OTHER: Behavioral, Psychological or Informational Intervention; OTHER: Questionnaire Administration. Primary outcome measures: Feasibility of adding hunger training (HT) to Diabetes Prevention Program (DPP) as assessed by recruitment rate , Up to 2 years; Feasibility of adding hunger training (HT) to Diabetes Prevention Program (DPP) as assessed by drop-out rates , Up to 2 years; Feasibility of adding hunger training (HT) to Diabetes Prevention Program (DPP) as assessed by completion rates , Up to 2 years. Brief summary: This pilot trial studies how well a diabetes prevention program with or without hunger training works in helping to lower breast cancer risk in obese participants. A diabetes prevention program involves learning about and receiving materials on different strategies to encourage weight loss, and hunger training involves learning how to recognize hunger. It is not yet known whether adding hunger training to a diabetes prevention program helps participants control their weight that could reduce the risk of some cancers.