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Spots Global Cancer Trial Database for Optimizing Veteran-Centered Prostate Cancer Survivorship Care

The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Optimizing Veteran-Centered Prostate Cancer Survivorship Care

Official Title: Optimizing Veteran-Centered Prostate Cancer Survivorship Care

Study ID: NCT01900561

Conditions

Prostate Cancer

Study Description

Brief Summary: This study will provide much needed information about how to optimize the quality of care and quality of life of Veterans who are survivors of prostate cancer.

Detailed Description: Although there are nearly 150,000 prostate cancer survivors in the VA, there has been little research to understand and improve survivorship care for this large population of Veterans. A substantial proportion of prostate cancer survivors in the general population have significant side effects from treatment (surgery or radiation therapy) that often persist for years, including incontinence, erectile dysfunction, and metabolic syndrome, all of which can contribute to decreased quality of life. The investigators' pilot data suggests that VA prostate cancer survivors experience similar or worse symptom burden to that of the general population of survivors. To address the need to improve patient-centered survivorship care management for Veterans with prostate cancer, the investigators propose a 4 year study with two aims: 1) to conduct a randomized controlled trial to compare a personally tailored automated telephone symptom management intervention for improving symptoms and symptom self-management to usual care. The investigators expect that those in the intervention group will have more confidence in symptom self-management and better symptom self-management and prostate cancer quality of life following the intervention, and that these outcomes will translate to more efficient use of services for these Veterans, and 2) to compare utilization of services among those in the intervention group to those in the control group.

Eligibility

Minimum Age: 40 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: MALE

Healthy Volunteers: No

Locations

VA Ann Arbor Healthcare System, Ann Arbor, MI, Ann Arbor, Michigan, United States

St. Louis VA Medical Center John Cochran Division, St. Louis, MO, Saint Louis, Missouri, United States

Louis Stokes VA Medical Center, Cleveland, OH, Cleveland, Ohio, United States

VA Pittsburgh Healthcare System University Drive Division, Pittsburgh, PA, Pittsburgh, Pennsylvania, United States

Contact Details

Name: Sarah T Hawley, PhD MPH BA

Affiliation: VA Ann Arbor Healthcare System, Ann Arbor, MI

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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