The purpose is to examine the feasibility and preliminary effectiveness of the role of a
personal trainer for non-metastatic breast cancer survivors to improve physical activity and
well-being (in terms of quality of life).
Other: Exercise regimen
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Full eligibility criteria for NCT02770781
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Post active breast cancer therapy (e.g. surgery and/or chemotherapy and/or radiation therapy), but may still be undergoing maintenance cancer therapy.
Free of macro-metastatic disease
Sedentary pre-cancer diagnosis: Those individuals not participating in a regular exercise program or not meeting the minimal physical activity recommendations from the General Surgeon which is accumulating 30 minutes or more of moderate physical activity on most days of the week
Ability to provide informed consent
Ability to provide a written physician's clearance
Patients must be new to the Survivorship Clinic (within first 12 months).
Medical conditions that would preclude participation in a weight-training program.
Those who plan on relocating outside the Greater Pittsburgh Area in the next 3 months of intervention.
All locations for NCT02770781
United States (1)
University of Pittsburgh, Department of Medicine.
Pittsburgh, Pennsylvania, United States, 15232
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View full eligibility
Tris trial is registered with FDA with number: NCT02770781. The sponsor of the trial is University of Pittsburgh and it is looking for 80 volunteers for the current phase.
Official trial title: Feasibility Study of the Addition of a Personal Trainer to the Post-Treatment Regimen of Breast Cancer Survivors
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