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Breast Cancer Survivor Educational Intervention

NCT05700396 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 7

Last updated 2025-04-01

No results posted yet for this study

Summary

The goal of this study is to test a 6-week virtual education program among Black breast cancer survivors. The virtual program includes sessions on physical activity, goal setting, nutrition, sleep, stress, and social connections.

Conditions

  • Breast Cancer
  • Breast Neoplasms
  • Breast Carcinoma
  • Breast Cancer Female

Interventions

BEHAVIORAL

Breast Cancer Survivor Education Program

Weekly sessions via Zoom platform with study staff.

Sponsors & Collaborators

  • American Cancer Society, Inc.

    collaborator OTHER

  • Pfizer

    collaborator INDUSTRY

  • Massachusetts General Hospital

    lead OTHER

Principal Investigators

  • Erica Warner, MPH, ScD · Massachusetts General Hospital

  • Amy Comander, MD · Massachusetts General Hospital

  • Naomi Ko, MD · Boston Medical Center

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
22 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-02-28
Primary Completion
2023-12-31
Completion
2023-12-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05700396 on ClinicalTrials.gov