Behavioral Weight Loss and Exercise After Treatment (BEAT)

Status unconfirmed · Not applicable

Conditions studied: Breast Cancer

In brief

Overweight and physically inactive breast cancer survivors are at increased risk of breast cancer recurrence and mortality. Cancer treatment-related changes that likely mediate weight loss and exercise success include the long term effects such as fatigue, psychological distress and impaired executive (cognitive) function. This study will explore the variability in how breast cancer survivors respond to a behavioral weight loss intervention. The primary objectives include determining the degree to which success with a behavioral weight loss intervention in overweight breast cancer survivors is explained by measures of executive function as measured with task performance at 6 and 12 months and associated brain function imaging (fMRI), collected at baseline only.Additionally, the study is designed to determine the degree to which selected measures of cancer-related symptoms account for variance in the success of breast cancer survivors at 6 and 12 months following entry into a behavioral weight loss and exercise intervention.

Key facts

Study ID

NCT02052115

Run by

University of Vermont

People needed

80

Starts

2014-01-01

Expected to finish

2016-12-01

Last updated by the study team

2014-12-03

Who can join

Age: 21 and older, up to 69. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Breast cancer diagnosis
• Received surgery +/- chemotherapy +/- radiation for treatment of a Stage I, II or III breast cancer. Ongoing treatment with monoclonal antibodies and/or anti-estrogen therapy is acceptable
• Completion of initial therapy 6 weeks prior to study initiation
• BMI of 27-45 kg/m\^2

You may not qualify if…

• Prior diagnosis of malignancy other than non-melanoma skin cancer (i.e. prior non-melanoma skin cancer is not an exclusion criteria)
• Medical conditions that limit food choices such as celiac sprue or inflammatory bowel disease
• Inability to walk on flat ground (or a treadmill) at 2.5 mph for 5 minutes
• Age <21 and >70
• Presence of body metal
• Psychotic or central nervous system impairment that would limit compliance with study requirements, including dementia
• Evidence of metastatic disease
• Symptomatic heart disease (chest pain or equivalent with activity)
• Exercise limiting pulmonary disease or need for oxygen to exercise
• Individuals taking mood stabilizing medications including: Lithium, valproic acid, also called divalproex sodium (Depakote), carbamazepine (Tegretol), lamotrigine (Lamictal), oxcarbazepine (Trileptal), olanzapine (Zyprexa), aripiprazole (Abilify), risperidone (Risperdal), ziprasidone (Geodon), clozapine (clorazil)
• Participants with an active neurologic disorder that affects the central nervous system, including seizures, and Parkinson's disease
• Weight loss of >10 lbs in the previous 6 months
• Participation in > 150 minutes of moderate intensity activity by self report, unless activity level by accelerometer is less than 150 minutes of moderate intensity activity

Where it is running

• Vermont Cancer Center — Burlington, Vermont, United States (enrolling)

Full record on ClinicalTrials.gov

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