Weight Management Among Breast Cancer Survivors

Not Applicable

Completed

• Conditions: Body Weight
• Interventions: Behavioral: Diet Intake Messages; Behavioral: Behavioral Counseling

• Registration Number: NCT02387671
• Lead Sponsor: Boston Medical Center

Brief Summary

The long-term goal of this research is to develop, evaluate and implement effective mHealth technology interventions that improve cancer management outcomes by changing lifestyle behaviors among urban health- disparity facing populations. To accomplish this goal, the investigators will need to determine the feasibility and preliminary efficacy of an intervention in which breast cancer survivors receive counseling about lifestyle behaviors (weight, nutrition, and physical activity) from a health counselor trained in evidenced-based behavioral counseling methods.

Detailed Description

Tremendous advances in detection and treatment of breast cancer have led to an increasingly large cohort of survivors focused on health promotion and reducing the risk of recurrence. While adjuvant therapy, such as hormone therapy, is often used to prevent cancer recurrence, modification of lifestyle is an effective tool to increase quality of life, prevent future cancer recurrence and increase long-term health. However, translating these recommendations into population-wide, inexpensive, sustainable programs for cancer survivors has to date proven largely unrealized. These programs are particularly needed in health disparity-facing populations (i.e., low socio-economic status and/or racial/ethnic minority groups) due to the high burden of cancer incidence and mortality they face. Limited translation is due to many factors including the complexity of lifestyle habits, high patient burden of many behavioral interventions, low levels of engagement and adherence to interventions, and the lack of integration of behavior change tools into daily lifestyles. In this context, there is great promise of tools that are mobile, simple, and embedded into daily life routines. The long-term goal of this research program is to develop, evaluate and implement effective mHealth technology interventions that improve cancer management outcomes by changing lifestyle behaviors among urban health- disparity facing populations.

The mHealth intervention for cancer survivors devised by the investigators consists of several components: 1) a commercially available smart phone app that captures patients' behavioral data (steps, sleep, weight) using devices (a FitBit and a FitBit scale), 2) text messages to participants to collect additional data (foods eaten, eating habits), and 3) phone sessions with a non-professionally trained health counselor about diet and physical activity behaviors.

The investigators propose to test the feasibility and preliminary outcomes on weight, behaviors, psychological factors as well as participant engagement in the intervention of our mHealth counseling intervention among 20 breast cancer survivors.

Study Timeline

• Status Verified: 2015-01
• Study Start: 2015-02
• Study First Submitted: 2015-02-12
• Study First Submitted QC: 2015-03-12
• Study First Posted: 2015-03-13
• Primary Completion: 2015-07
• Study Completion: 2015-07
• Last Update Submitted: 2016-06-29
• Last Update Posted: 2016-07-01

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 10

Inclusion Criteria

• Willing to participate in intervention by sharing FitBit account information (log in/password) with study team
• 6 months or more since receiving cancer treatment including surgery, radiation, or chemotherapy (self-reported)
• 2 or more years post breast cancer diagnosis (self-reported)
• Current ownership of an iOS or Android based platform smartphone and home wifi
• Age 18 and above
• Ability to speak and read in English
• Overweight or obese (body mass index ≥ 25)
• Female

Exclusion Criteria

• Medical conditions including dementia, active cancer, anorexia or any other condition in the opinion of the investigator makes the participant unsuitable for inclusion in the study
• Presence of a pacemaker or other internal medical device
• Those with contraindications for physical activity
• Pregnant women
• Inability to easily navigate programs on a smartphone

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
mHealth Platform	Diet Intake Messages	The primary interventions employed in the study are wifi enabled tracking devices, text message communications and behavioral counseling.
mHealth Platform	Behavioral Counseling	The primary interventions employed in the study are wifi enabled tracking devices, text message communications and behavioral counseling.

Primary Outcome Measures

Name	Time	Method
Body Weight	8 weeks	Participants will register daily body weight measurements during the 8-week study period. Weight will be recorded in units of pounds using the FitBit wifi compatable. All data will be synced to the participants' FitBit account and monitored by the study team.

Trial Locations

Locations (1)

Boston Medical Center; 🇺🇸 Boston, Massachusetts, United States