Neoplasms

All Conditions

Skin and Connective Tissue Diseases

Carcinoma

Breast Neoplasms

Breast Diseases

Skin Diseases

Participants will complete study procedures as outlined:

- 6 weekly sessions of a modified version of the PAVING the Path to Wellness education program.

Weekly sessions via Zoom platform with study staff.

Breast Cancer Survivor Education Program

Erica Warner, MPH, ScD

Audra Hite

Amy Comander, MD

Naomi Ko, MD

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.

This six-week feasibility study will evaluate a virtual support and education program among up to 15 Black female breast cancer survivors. Participants will be asked to attend a 90 minute group session once a week for 6 weeks and complete surveys pre and post intervention surveys to ascertain study endpoints. This study is supported by funding from Pfizer and in-kind support from the American Cancer Society, Inc.

Breast Cancer Survivor Educational Intervention

Increasing Receipt of Guideline Concordant Survivorship Care Among Black Breast Cancer Survivors Through Patient Education

The Dana-Farber / Harvard Cancer Center encourages and supports the responsible and ethical sharing of data from clinical trials. De-identified participant data from the final research dataset used in the published manuscript may only be shared under the terms of a Data Use Agreement. Requests may be directed to: \[contact information for Sponsor Investigator or designee\]. The protocol and statistical analysis plan will be made available on Clinicaltrials.gov only as required by federal regulation or as a condition of awards and agreements supporting the research.

Defined as the number of recruited participants who initiate intervention program.

Defined as the amount of time to target accrual goal.

Defined as the number of eligible participants required to recruit required sample size.

Defined as the number of participants who attend at least 5 of 6 sessions.

Proportion of participants "very satisfied" or "completely satisfied" with intervention. Defined successful if true of 80% of participants.

Proportion of participants completing evaluation surveys each at baseline and week 6.

Self-Efficacy for symptom self-management will be assessed using Symptom-Management Self-Efficacy Scale-Breast Cancer

Intention to Receive post-treatment Surveillance Mammography will be assessed using Follow-Up Care Use and Health Outcomes of Cancer Survivors (FOCUS) Survey

Physical Activity Goal Change will be assessed using Follow-Up Care Use and Health Outcomes of Cancer Survivors (FOCUS) Survey

Dietary Behavior Goal Change will be assessed using Follow-Up Care Use and Health Outcomes of Cancer Survivors (FOCUS) Survey

Unmet information Needs will be assessed using Follow-Up Care Use and Health Outcomes of Cancer Survivors (FOCUS) Survey

Study title	NCT ID	Conditions	Interventions	Eligibility	Organization	Link
Breast Cancer Survivor Educational Intervention	NCT05700396	Breast Cancer Breast Neoplasm... Breast Carcinom... Breast Cancer F...	Breast Cancer S...	22 Years -	Massachusetts General Hospital
Breast Cancer Survivor Educational Intervention	NCT05700396	Breast Cancer Breast Neoplasm... Breast Carcinom... Breast Cancer F...	Breast Cancer S...	22 Years -	Massachusetts General Hospital

Spots Global Cancer Trial Database for breast cancer survivor education program