Lifestyle Intervention for High Risk Cancer Survivors
NCT01508273 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1150
Last updated 2016-12-02
Summary
The goal of this behavioral research study is to find out more about the health behaviors of cancer survivors. Researchers want to understand the cultural, social, and environmental factors related to physical activity and personal diet. Researchers also want to learn if cancer survivors who take part in lifestyle interventions have better overall health and quality of life than those who do not take part in these interventions.
Conditions
Interventions
- BEHAVIORAL
-
Exercise Program
Resistance training bands, guidebook, and pedometer given at baseline visit. Internet-based curriculum access given to teach goal-setting, overcoming barriers to physical activity, self-management strategies, and time-management skills. Access given website that will allow participant to track exercise behavior and help set goals.
- BEHAVIORAL
-
Website
Website access given that allows participant to track exercise behavior and help to set goals.
- BEHAVIORAL
-
Exercise DVD
Participants receive chair-based exercise DVD. Participants in this chair-based exercise program for a total of 8 weeks.
- BEHAVIORAL
-
Survey
Exercise Intervention Program Group : Survey completion monthly about attitudes and beliefs about physical activity. Sedentary Behavior and Dietary Intervention Group: Survey completion monthly attitudes and beliefs about sedentary behavior and dietary intake.
- BEHAVIORAL
-
Self-Report Assessments
Self-report assessments given about quality of life and physical assessments of balance and coordination.
Sponsors & Collaborators
-
National Cancer Institute (NCI)
collaborator NIH -
M.D. Anderson Cancer Center
lead OTHER
Principal Investigators
-
Richard A. Hajek, PHD, MS, BA · M.D. Anderson Cancer Center
Study Design
- Allocation
- RANDOMIZED
- Purpose
- SUPPORTIVE_CARE
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 80 Years
- Sex
- FEMALE
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2012-05-31
- Primary Completion
- 2015-12-31
- Completion
- 2015-12-31
Countries
- United States
Study Locations
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