Keyword: "prostate cancer"

16 items were found with the keyword "prostate cancer".

  • Building Your New Normal VA

    PI: Sarah T. Hawley, PhD, MPH

    The over-arching goal of the study is to determine whether an intervention using highly personalized automated telephone monitoring and self-management support calls paired with tailored print material can effectively improve Veteran-centered outcomes for prostate cancer survivors. (09/01/2013 - 08/31/2017)

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  • Making the Choice - VA

    PI: Angela Fagerlin, PhD

    A current priority for VA research is "Healthcare Informatics to Improve Veteran Care Healthcare." This priority area recognizes the critical importance of developing effective technological tools for Veterans to improve their understanding of and capacity to be actively involved in shared decision making about key health issues. Making The Choice - VA develops new materials specifically for VA patients who have prostate cancer. The tool helps in shared and informed decision-making related to prostate cancer treatment options and outcomes. (01/01/2011 - 09/30/2011)

  • Building Your New Normal

    PI: Ted A. Skolarus, MD, MPH

    Building Your New Normal tests two novel approaches to improve the quality of post-treatment follow-up for prostate cancer survivors: 1) IVR (interactive voice response)-administered EPIC and 2) tailored versions of Michigan Cancer Consortium (MCC) guidelines for patients and their primary care providers (10/01/2010 - 09/30/2011)

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  • Prostate Cancer Recurrence Risk Decision Aid

    PI: Daniel A. Hamstra, PhD, MD

    Approximately 10-30% of men who undergo external beam radiation for localized prostate cancer see rising PSA scores following treatment. Some of these men need androgen deprivation therapy (ADT) as salvage treatment. ADT is not curative and has significant side effects that impact quality of life (QOL). These facts must be balanced against its clinical need. The decision to initiate hormonal therapy is driven more by patient anxiety and less by clinical parameters. Thus, men need to better understand how their PSA values and likelihood of recurrence will change over time. A novel computer model, based on 2,386 patients previously treated, provides this information. This project aims to develop and test methods of communicating this information to patients and to determine how patients use it in their treatment decisions. (09/01/2010 - 08/31/2012)

  • Narrative Video Library

    PI: Borsika Rabin, PhD, MPH, PharmD

    This project aims to develop an online library of video vignettes that highlight a discussion with a leading researcher or practitioner who describe one problem in the process of dissemination and implementation (D&I) and show viewers how he/she solved the problem. (09/01/2010 - 08/31/2011)

  • Discussing the Choice

    PI: Angela Fagerlin, PhD , Peter A. Ubel, MD

    DVDs demonstrate to patients some of the issues that might arise during their prostate cancer diagnosis visit that may prevent them from sharing in the decision of what treatment to choose. The DVDs also provide solutions that would allow for patients' participation in the treatment decision making process. (09/01/2008 - 08/31/2013)

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  • CECCR2 - Center of Excellence In Cancer Communications Research II

    PI: Victor J. Strecher, PhD, MPH

    The purpose of the University of Michigan Center of Excellence in Cancer Communications Research (CECCR) is to develop an efficient, theory-driven model for generating tailored health behavior interventions for many health behaviors and socio-demographic populations. (09/01/2008 - 08/31/2013)

  • Making the Choice - Audio and Internet

    PI: John T. Wei, MD, MS

    This project is an adaptation of Making the Choice. We revise the paper-based decision aid and develop alternative media formats (audiotape- and Internet-based versions) of the paper based decision aid to increase distribution and utilization. We also test the paper, audiotape, and Internet-based decision aids in an appropriate population of patients to provide pilot data on the tools' efficacy for improving patient knowledge. (09/30/2002 - 09/29/2004)

  • Making the Choice

    PI: John T. Wei, MD, MS

    Making the Choice is a booklet to help men better understand prostate health and the issues surrounding prostate cancer testing. (09/30/2002 - 09/29/2004)

  • FOCUS Prostate

    PI: Laurel L. Northouse, PhD, RN, FAAN

    This study tests the effectiveness of a family-based program of care in improving clinical outcomes, and tests the ability of a model to predict which patients and spouses are at increased risk of poorer quality of life. (12/15/2000 - 03/31/2001)

  • Health'o'Vision CD-ROMs

    PI: Victor J. Strecher, PhD, MPH

    This project makes available a two-disc compilation of nine of the twelve health topics (the topics that are completed to date) that appear on the Michigan "Health'o'Vision" kiosks. (01/01/1998 - 09/30/1999)

  • Prostate Cancer Decision-Making

    PI: Robert C. Burack, MD, MPH

    This project is focused on creating a booklet to help men better understand prostate health and the issues surrounding prostate cancer testing. (09/01/1996 - 10/31/1997)

  • Health'o'Vision

    PI: Victor J. Strecher, PhD, MPH

    The Michigan Interactive Health Kiosk Demonstration Project project involves creating and disseminating twelve multimedia health programs.  Collectively known as Health'o'Vision, topics include cancer prevention and screening, disease management, and general health practices to live a healthy life. Channels are created for both adults and adolescents. One hundred kiosks are deployed in a variety of settings throughout the State of Michigan for use by the general public. (01/01/1996 - 09/30/2000)

  • The Prostate Cancer Screening Channel

    PI: Victor J. Strecher, PhD, MPH

    This project aims to create a channel for the Michigan Interactive Health Kiosk Project on prostate cancer symptoms, testing, and treatment options. (01/01/1996 - 09/30/1997)

  • FOCUS Triage

    PI: Laurel L. Northouse, PhD, RN, FAAN

    Focus Triage tests if family dyads randomly assigned to either a brief or extensive family-based program of care (FOCUS Program) have better patient and caregiver outcomes than dyads randomly assigned to usual care. Outcomes being studied: appraisal factors (i.e., appraisal of illness/caregiving, uncertainty, hopelessness), coping resources (coping strategies, interpersonal relationships, self-efficacy), and quality of life domains (emotional, social, physical, and functional).This study also examines if patientsí risk for distress and other factors moderate the effect of the brief or extensive program on outcomes.