NCT07137468

Brief Summary

To learn about breast cancer survivors' and their family members' knowledge of and interest in learning about environmental exposures related to personal care products. Researchers also want to learn if there is a link between excessive weight and chemicals that may affect hormones.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for all trials

Timeline
20mo left

Started Jan 2026

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress17%
Jan 2026Dec 2027

First Submitted

Initial submission to the registry

August 15, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

August 22, 2025

Completed
5 months until next milestone

Study Start

First participant enrolled

January 6, 2026

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2027

Last Updated

April 27, 2026

Status Verified

April 1, 2026

Enrollment Period

2 years

First QC Date

August 15, 2025

Last Update Submit

April 22, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Outcome Measure

    Questionnaires/Videos

    Through study completion; an average of 1 year

Study Arms (3)

Pre-Focus Group Survey

Before your focus group session, you will complete computer-based surveys about your age, biological sex, gender, income, highest level of education, marital status, insurance status, and health behaviors. The online surveys may take up to 40 minutes to complete.

Other: Surveys

Focus Group Session

After completing the pre-focus group surveys, you will be assigned to a focus group. The focus group will include a warm-up discussion (10 minutes), a short audiovisual presentation (5 minutes) describing endocrine-disrupting chemicals (EDCs), and open-ended questions facilitating discussions on environmental exposures and personal care product usage and ALAC program from your perspective (75 minutes). Focus groups will occur by Zoom video conferencing and will be audio- and video-recorded. The recording will be transcribed (written down) word-for-word, but without your name or any other identifying information. The digital audio and video files will be destroyed after they are transcribed.

Other: Video

Post-Focus Group Survey

After your focus group session, you will complete a computer-based survey to help researchers understand the products you use and things that you do in your everyday life, provide urine samples, and wear a wristband.

Other: Surveys

Interventions

VideoOTHER

Focus group sessions and community forums will be conducted via videoconference (Zoom)

Focus Group Session
SurveysOTHER

Electronic surveys will completed via REDCap.

Post-Focus Group SurveyPre-Focus Group Survey

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

MD Anderson Cancer Center

You may qualify if:

  • Be a resident of Acres Home community
  • Be 18 years of age and older
  • Self-report a breast cancer diagnosis including subtypes OR be a family member of a survivor
  • If a breast cancer survivor: current or former participants of the ALAC program
  • Able to communicate in English

You may not qualify if:

  • Self-report metastatic breast cancer diagnosis
  • Unable to communicate in English
  • Not a breast cancer survivor or family member of a survivor

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The University of Texas M. D. Anderson Cancer Center

Houston, Texas, 77030, United States

RECRUITING

Related Links

MeSH Terms

Conditions

Breast Neoplasms

Interventions

Surveys and QuestionnairesVideotape Recording

Condition Hierarchy (Ancestors)

Neoplasms by SiteNeoplasmsBreast DiseasesSkin DiseasesSkin and Connective Tissue Diseases

Intervention Hierarchy (Ancestors)

Data CollectionEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public HealthTape RecordingAudiovisual AidsEducational TechnologyTechnologyTechnology, Industry, and AgricultureTelevision

Study Officials

  • Dede Teteh-Brooks, DRPH

    M.D. Anderson Cancer Center

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Dede Teteh-Brooks, DRPH

CONTACT

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 15, 2025

First Posted

August 22, 2025

Study Start

January 6, 2026

Primary Completion (Estimated)

December 31, 2027

Study Completion (Estimated)

December 31, 2027

Last Updated

April 27, 2026

Record last verified: 2026-04

Locations