Literature DB >> 24645337

Monitoring of health-related quality of life and symptoms in prostate cancer survivors: a randomized trial.

Kimberly M Davis, David Dawson, Scott Kelly, Sara Red, Sofiya Penek, John Lynch, Sean Collins, Barlow Lynch, Michael Porrazzo, Michael Bass, Kathryn L Taylor.   

Abstract

BACKGROUND: Routine symptom and health-related quality of life (HRQOL) assessments can engage patients, give provider feedback, and improve doctor/patient communication.
OBJECTIVE: We compared the impact of a technology-assisted symptom monitoring system versus usual care on HRQOL and doctor/patient communication in early-stage prostate cancer (PCa) survivors.
METHODS: Men (N = 94) were on average 62-years old, mostly African American (AA; 61.7%), and 10-19 months post-treatment. They were randomized to symptom monitoring plus feedback (SM + F; n = 49) or usual care (UC; n = 45). SM+F participants completed a 12-item telephoneassisted monitoring intervention. All participants completed a baseline and 2 follow-up interviews.
RESULTS: Among the SM+F participants, perceptions of the monitoring system were positive: 97.1% endorsed it as easy/very easy to use and 85% felt all patients could benefit from it. At baseline, men reported favorable general and cancer-specific HRQOL and doctor/patient communication, but poorer urinary and sexual function. Although there was no overall impact of the intervention, post hoc exploratory analyses indicated that among AA men, those who received SM+F improved relative to UC on doctor/patient communication (P < .05), general HRQOL (P < .06), and sexual function (P < .05). LIMITATIONS: Variability in survivor follow-up care, limited access to eligible participants, and minimal physician training in the use of reports likely decreased physician investment.
CONCLUSION: Overall, PCa survivors were receptive to this monitoring system. Exploratory analyses suggest that this technology-assisted monitoring system may be of particular benefit to African American men. Additional studies with larger samples, more intervention time-points, and increased physician training are needed to strengthen the intervention's impact.

Entities:  

Mesh:

Year:  2013        PMID: 24645337     DOI: 10.12788/j.suponc.0013

Source DB:  PubMed          Journal:  J Support Oncol        ISSN: 1544-6794


  8 in total

Review 1.  Patient-reported outcome use in oncology: a systematic review of the impact on patient-clinician communication.

Authors:  L Y Yang; D S Manhas; A F Howard; R A Olson
Journal:  Support Care Cancer       Date:  2017-08-28       Impact factor: 3.603

2.  Developing NaviCanPlan: A Mobile Web Resource Locator for Cancer Providers and Survivors.

Authors:  Deborah Vollmer Dahlke; Debra Kellstedt; Armin D Weinberg
Journal:  J Cancer Educ       Date:  2015-12       Impact factor: 2.037

Review 3.  Patient-reported outcome measurement implementation in cancer survivors: a systematic review.

Authors:  Surbhi Singhal; James Dickerson; Michael J Glover; Mohana Roy; Michelle Chiu; Timothy Ellis-Caleo; Gavin Hui; Carla Tamayo; Nele Loecher; Hong-Nei Wong; Lauren C Heathcote; Lidia Schapira
Journal:  J Cancer Surviv       Date:  2022-05-23       Impact factor: 4.442

Review 4.  Routine provision of feedback from patient-reported outcome measurements to healthcare providers and patients in clinical practice.

Authors:  Chris Gibbons; Ian Porter; Daniela C Gonçalves-Bradley; Stanimir Stoilov; Ignacio Ricci-Cabello; Elena Tsangaris; Jaheeda Gangannagaripalli; Antoinette Davey; Elizabeth J Gibbons; Anna Kotzeva; Jonathan Evans; Philip J van der Wees; Evangelos Kontopantelis; Joanne Greenhalgh; Peter Bower; Jordi Alonso; Jose M Valderas
Journal:  Cochrane Database Syst Rev       Date:  2021-10-12

5.  The association of long-term treatment-related side effects with cancer-specific and general quality of life among prostate cancer survivors.

Authors:  Kimberly M Davis; Scott P Kelly; George Luta; Catherine Tomko; Anthony B Miller; Kathryn L Taylor
Journal:  Urology       Date:  2014-06-26       Impact factor: 2.649

6.  Follow-up strategies following completion of primary cancer treatment in adult cancer survivors.

Authors:  Beverley L Høeg; Pernille E Bidstrup; Randi V Karlsen; Anne Sofie Friberg; Vanna Albieri; Susanne O Dalton; Lena Saltbæk; Klaus Kaae Andersen; Trine Allerslev Horsboel; Christoffer Johansen
Journal:  Cochrane Database Syst Rev       Date:  2019-11-21

7.  Quality of Patient-Provider Communication Among Cancer Survivors: Findings From a Nationally Representative Sample.

Authors:  Neetu Chawla; Danielle Blanch-Hartigan; Katherine S Virgo; Donatus U Ekwueme; Xuesong Han; Laura Forsythe; Juan Rodriguez; Timothy S McNeel; K Robin Yabroff
Journal:  J Oncol Pract       Date:  2016-10-31       Impact factor: 3.840

Review 8.  Patient outcomes, patient experiences and process indicators associated with the routine use of patient-reported outcome measures (PROMs) in cancer care: a systematic review.

Authors:  Caitlin Graupner; Merel L Kimman; Suzanne Mul; Annerika H M Slok; Danny Claessens; Jos Kleijnen; Carmen D Dirksen; Stéphanie O Breukink
Journal:  Support Care Cancer       Date:  2020-09-02       Impact factor: 3.603

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.