Literature DB >> 30266777

The top research questions asked by people with lived depression experience in Alberta: a survey.

Lorraine J Breault1, Katherine Rittenbach2, Kelly Hartle2, Robbie Babins-Wagner2, Catherine de Beaudrap2, Yamile Jasaui2, Emily Ardell2, Scot E Purdon2, Ashton Michael2, Ginger Sullivan2, Aakai'naimsskai'piiaakii Sharon Ryder Unger2, Lorin Vandall-Walker2, Brad Necyk2, Kiara Krawec2, Elizabeth Manafò2, Ping Mason-Lai2.   

Abstract

BACKGROUND: To support patient-oriented setting of priorities for depression research in Alberta, the Patient Engagement Platform of the Alberta Strategy for Patient Oriented Research's Support for People and Patient-Oriented Research and Trials Unit and Alberta Health Services' Addiction and Mental Health Strategic Clinical Network, along with partners in addictions and mental health, designed the Alberta Depression Research Priority Setting Project. The aim of the project was to survey patients, caregivers and clinicians/researchers in Alberta about what they considered to be the most important unanswered questions about depression.
METHODS: The project adapted the James Lind Alliance Priority Setting Partnership method into a 6-step process to gather and prioritize questions about depression posed by people with lived depression experience, which included patients, caregivers, clinicians and health care practitioners.
RESULTS: Implementation of the project, from initial data collection to final priority setting, took 10 months (August 2016 to June 2017). A total of 445 Albertans with lived experience of depression participated, ultimately identifying 11 priority depression research questions spanning the health continuum, life stages, and treatment and prevention opportunities.
INTERPRETATION: This project is a fundamental step that has the potential to positively influence depression research. Including the voices of Albertans with lived experience will create advantages for depression research for Albertans, researchers and research funders, and for patient engagement in the research enterprise overall. Copyright 2018, Joule Inc. or its licensors.

Entities:  

Year:  2018        PMID: 30266777      PMCID: PMC6182109          DOI: 10.9778/cmajo.20180034

Source DB:  PubMed          Journal:  CMAJ Open        ISSN: 2291-0026


  26 in total

1.  Patient participation as dialogue: setting research agendas.

Authors:  Tineke A Abma; Jacqueline E W Broerse
Journal:  Health Expect       Date:  2010-06       Impact factor: 3.377

2.  Exploring facilitators and barriers to individual and organizational level capacity building: outcomes of participation in a community priority setting workshop.

Authors:  Laura M Flaman; Candace I J Nykiforuk; Ronald C Plotnikoff; Kim Raine
Journal:  Glob Health Promot       Date:  2010-06

Review 3.  Lessons Learned from Developing a Patient Engagement Panel: An OCHIN Report.

Authors:  Jill Arkind; Sonja Likumahuwa-Ackman; Nate Warren; Kay Dickerson; Lynn Robbins; Kathy Norman; Jennifer E DeVoe
Journal:  J Am Board Fam Med       Date:  2015 Sep-Oct       Impact factor: 2.657

4.  Priority setting and cardiac surgery: a qualitative case study.

Authors:  Nancy A Walton; Douglas K Martin; Elizabeth H Peter; Dorothy M Pringle; Peter A Singer
Journal:  Health Policy       Date:  2006-06-06       Impact factor: 2.980

5.  Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support.

Authors:  Paul A Harris; Robert Taylor; Robert Thielke; Jonathon Payne; Nathaniel Gonzalez; Jose G Conde
Journal:  J Biomed Inform       Date:  2008-09-30       Impact factor: 6.317

6.  Public engagement in priority-setting: results from a pan-Canadian survey of decision-makers in cancer control.

Authors:  Dean A Regier; Colene Bentley; Craig Mitton; Stirling Bryan; Michael M Burgess; Ellen Chesney; Andy Coldman; Jennifer Gibson; Jeffrey Hoch; Syed Rahman; Mona Sabharwal; Carol Sawka; Victoria Schuckel; Stuart J Peacock
Journal:  Soc Sci Med       Date:  2014-10-18       Impact factor: 4.634

7.  Patient and Researcher Engagement in Health Research: A Parent's Perspective.

Authors:  Israel Amirav; Virginia Vandall-Walker; Jananee Rasiah; Laura Saunders
Journal:  Pediatrics       Date:  2017-09       Impact factor: 7.124

Review 8.  Patients' and clinicians' research priorities.

Authors:  Ruth J Stewart; Jenny Caird; Kathryn Oliver; Sandy Oliver
Journal:  Health Expect       Date:  2010-12-22       Impact factor: 3.377

9.  GRIPP2 reporting checklists: tools to improve reporting of patient and public involvement in research.

Authors:  S Staniszewska; J Brett; I Simera; K Seers; C Mockford; S Goodlad; D G Altman; D Moher; R Barber; S Denegri; A Entwistle; P Littlejohns; C Morris; R Suleman; V Thomas; C Tysall
Journal:  BMJ       Date:  2017-08-02

Review 10.  Patient engagement in Canada: a scoping review of the 'how' and 'what' of patient engagement in health research.

Authors:  Elizabeth Manafo; Lisa Petermann; Ping Mason-Lai; Virginia Vandall-Walker
Journal:  Health Res Policy Syst       Date:  2018-02-07
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  6 in total

1.  The Scleroderma Research Topics Survey for patients and health care professionals: A Scleroderma Patient-centered Intervention Network Project.

Authors:  Lydia Tao; Claire Fedoruk; Kimberly A Turner; Julie Cumin; Marie-Eve Carrier; Andrea Carboni-Jiménez; Mia R Pépin; Linda Kwakkenbos; Brett D Thombs
Journal:  J Scleroderma Relat Disord       Date:  2019-04-23

2.  Developing a program theory of patient engagement in patient-oriented research and the impacts on the health care system: protocol for a rapid realist review.

Authors:  Elaine Zibrowski; Shelagh McDonald; Heather Thiessen; Ray VanDusen; Catherine Boden; Tracey Carr; Donna Goodridge; Charlene Haver; Darcy Marciniuk; Christine Stobart; Tanya Verrall; Gary Groot
Journal:  CMAJ Open       Date:  2020-08-31

3.  Evidence available for patient-identified priorities in depression research: results of 11 rapid responses.

Authors:  Meghan Sebastianski; Michelle Gates; Allison Gates; Megan Nuspl; Liza M Bialy; Robin M Featherstone; Lorraine Breault; Ping Mason-Lai; Lisa Hartling
Journal:  BMJ Open       Date:  2019-06-28       Impact factor: 2.692

4.  Top 10 (plus 1) research priorities for expectant families and those with children to age 24 months in Alberta, Canada: results from the Family Research Agenda Initiative Setting (FRAISE) priority setting partnership project.

Authors:  Meredith Lee Brockway; Elizabeth Keys; Katherine Stuart Bright; Carla Ginn; Leslie Conlon; Stephanie Doane; Jacqueline Wilson; Lianne Tomfohr-Madsen; Karen Benzies
Journal:  BMJ Open       Date:  2021-12-09       Impact factor: 2.692

5.  What are the respiratory health research priorities in Alberta, Canada? A stakeholder consultation.

Authors:  Heather Sharpe; Lisa Cerato; Darlene Derech; Lisa Guirguis; Kathleen Hayward; Tara Lohmann; Joanna E MacLean; Elizabeth Manafo; Janice Paskey; Jananee Rasiah; Mark Rimkus; Syeda Kinza Rizvi; Gerry Robinson; Brent Seefried; Zeeyaan Somani; Mindy Tindall; Harissios Vliagoftis; Sachin R Pendharkar; Michael K Stickland
Journal:  BMJ Open       Date:  2022-06-23       Impact factor: 3.006

6.  Perceived Effectiveness and Motivations for the Use of Web-Based Mental Health Programs: Qualitative Study.

Authors:  Heidi Eccles; Molly Nannarone; Bonnie Lashewicz; Mark Attridge; Alain Marchand; Alice Aiken; Kendall Ho; Jianli Wang
Journal:  J Med Internet Res       Date:  2020-07-31       Impact factor: 5.428

  6 in total

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