Physical Activity and First Degree Female Relatives of Breast Cancer Patients
NCT ID: NCT03115658
Last Updated: 2017-04-14
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
27 participants
INTERVENTIONAL
2009-09-08
2011-01-28
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Walking Affecting Immunology and Quality of Life of Breast Cancer Patients
NCT02581956
Enhancing Exercise in Breast Cancer Survivors
NCT01849978
Effectiveness of a Cancer Center Based Physical Activity Intervention
NCT01173861
Studying Tailored Exercise Prescriptions in Breast Cancer Patients
NCT02802826
Physical Activity Intervention to Reduce Functional Health Disparities Among Breast Cancer Survivors
NCT02763228
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
OTHER
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Exercise Intervention
Participants met with a PhD level psychologist experienced with health behavior change, to set a personalized exercise goal and plan. Participants were told the studies' goal to engage in 150 minutes of moderate intensity or greater physical activity each week, based on the ACSM recommendations, but participants were allowed to set any personal goal. Participants were also instructed on how to self-monitor their physical activity.
After the initial meeting all other intervention components were sent through the mail. The intervention consists of three types of print material that were mailed: stage-matched manuals, tailored feedback report, and tip sheets.
Physical Activity
12 week print based intervention
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Physical Activity
12 week print based intervention
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Have a mother, sister, or daughter who was diagnosed with breast cancer
* Have not been diagnosed with any type of cancer except basal cell carcinoma
* Able to speak and read English
* Sedentary, defined as engaging in less than 90 minutes of moderate-intensity physical activity each week
Exclusion Criteria
* Presence of a known medical condition that would make physical activity unsafe
* History of a severe psychiatric illness
* Plans to move from the area in the next 3 months.
18 Years
65 Years
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of California, San Diego
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Sheri Hartman
Assistant Professor
References
Explore related publications, articles, or registry entries linked to this study.
Hartman SJ, Dunsiger SI, Marcus BH. A pilot study of a physical activity intervention targeted towards women at increased risk for breast cancer. Psychooncology. 2013 Feb;22(2):381-7. doi: 10.1002/pon.2101. Epub 2011 Dec 2.
Hartman SJ, Rosen RK. Breast cancer relatives' physical activity intervention needs and preferences: qualitative results. BMC Womens Health. 2017 May 19;17(1):36. doi: 10.1186/s12905-017-0392-0.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2050-09
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.