LEVEL UP: Video Games for Activity in Breast Cancer Survivors

The University of Texas Medical Branch, Galveston

Overview

The purpose of this study is to test an intervention that uses home console video games to encourage increased physical activity among postmenopausal breast cancer survivors.

This research project includes qualitative and quantitative formative research leading to a randomized controlled feasibility trial of a video game-based physical activity intervention. First, we will investigate exercise protocols implemented over 6 weeks in 20 breast cancer survivors. We will choose a console and six games for inclusion in the trial, based on measured energy expenditure and enjoyment. We will create refined exercise protocols using these games and insights from participants. Second, we will test an intervention that uses active video games for implementation of motivating exercise and provision of behavioral tools (e.g., tracking of progress towards goals). Participants in a pre-pilot trial (N = 10) will receive weekly brief telephone counseling over 6 weeks. Feasibility measurement will include attrition, self-reported acceptability, and objective measures of video game play taken from game console data.

Study Type

INTERVENTIONAL

Allocation

Purpose

SUPPORTIVE_CARE

Masking

SINGLE

Conditions

Breast Cancer Obesity

Interventions

Physical activity interventionBEHAVIORAL

Participants will receive counseling on self-regulatory skill building that has been adapted to complement the video games used. We anticipate that the games used will consist of fitness, sports, and dance games and will be played on a Wii U console. The games played will be chosen by each participant from a pool of potential appropriate games.

Eligibility

Sex: FEMALEMin age: 45 YearsMax age: 75 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Female * Aged 45 - 75 * Diagnosed with breast cancer within the past 10 years Exclusion Criteria: * Chemotherapy or radiation treatment in the past six months * Surgery in the past six months * Evidence of disease recurrence * Unable to read and understand English * Unable to see a TV screen from several feet away * Unable to find transportation to the study location * No Internet access in the home (only for intervention portion of the study) * Participant is active (60 minutes of moderate-vigorous intensity activity per week or more) * BMI is under 18.5 kg/m2 or over 40 kg/m2 * Participant reports psychological issues that would interfere with study completion. Examples will be provided to illustrate potential psychological issues, such as dementia or schizophrenia. * Inadequate performance on Senior Fitness Test, indicating inability to engage in video game exercise procedures (total score \< 9 out of 12) * Report a heart condition, chest pain during periods of activity or rest, loss of consciousness, etc. on the Physical Activity Readiness Questionnaire (PAR-Q), unless cleared by their physician * Unable to walk, jump, and jog as may be required by some games (self-report) * Report current symptoms of alcohol or substance dependence * Plans to move away from the Galveston-Houston area or to be out of town for more than 1 week during the study period * Unwillingness to report drugs taken for comorbidities such as hypertension or diabetes * Stroke, hip fracture, hip or knee replacement, or spinal surgery in the past 6 months * Report a history of orthopedic complications that would prevent optimal participation in the physical activities prescribed (e.g., heel spurs, severe arthritis) * Clinical judgment concerning safety * Currently participating in a physical activity or weight program/research study * Currently pregnant or nursing * No TV is available in the participant's home * Currently on a weight loss diet or has lost more than 5% body weight in the previous 6 months * Current smoker * Game console to be used in the study is already available in the home * Another member of the household is a participant or staff member on this trial

Locations (1)

University of Texas Medical Branch

Galveston, Texas, United States

Outcomes

Primary Outcomes

Change in physical activity from baseline to 6 weeks

Minutes of moderate-vigorous physical activity measured over a 7 day period

Time frame: 6 weeks

Secondary Outcomes

Change in physical fitness from baseline to 6 weeks

We will use a six minute walk test to measure fitness

Time frame: 6 weeks

Change in weight from baseline to 6 weeks

Weight will be measured using a calibrated scale

Time frame: 6 weeks

Change in motivation from baseline to 6 weeks

We will measure autonomous motivation (intrinsic, integrated, identified, etc.) specific to physical activity

Time frame: 6 weeks

Change in body function from baseline to 6 weeks

We will use the Senior Fitness Test to measure strength and body function

Time frame: 6 weeks

Change in quality of life from baseline to 6 weeks

We will use the Functional Assessment of Cancer Therapy - Breast measure to quantify quality of life

Time frame: 6 weeks

Data from ClinicalTrials.gov

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