Literature DB >> 25565585

Development, Content Validity, and User Review of a Web-based Multidimensional Pain Diary for Adolescent and Young Adults With Sickle Cell Disease.

Nitya Bakshi1, Jennifer N Stinson, Diana Ross, Ines Lukombo, Nonita Mittal, Saumya V Joshi, Inna Belfer, Lakshmanan Krishnamurti.   

Abstract

BACKGROUND: Vaso-occlusive pain, the hallmark of sickle cell disease (SCD), is a major contributor to morbidity, poor health-related quality of life, and health care utilization associated with this disease. There is wide variation in the burden, frequency, and severity of pain experienced by patients with SCD. As compared with health care utilization for pain, a daily pain diary captures the breadth of the pain experience and is a superior measure of pain burden and its impact on patients. Electronic pain diaries based on real-time data capture methods overcome methodological barriers and limitations of paper pain diaries, but their psychometric properties have not been formally established in patients with SCD.
OBJECTIVES: To develop and establish the content validity of a web-based multidimensional pain diary for adolescents and young adults with SCD and conduct an end-user review to refine the prototype.
MATERIALS AND METHODS: Following identification of items, a conceptual model was developed. Interviews with adolescents and young adults with SCD were conducted. Subsequently, end-user review with use of the electronic pain diary prototype was conducted.
RESULTS: Two iterative cycles of in-depth cognitive interviews in adolescents and young adults with SCD informed the design and guided the addition, removal, and modification of items in the multidimensional pain diary. Potential end-users provided positive feedback on the design and prototype of the electronic diary.
CONCLUSION: A multidimensional web-based electronic pain diary for adolescents and young adults with SCD has been developed and content validity and initial end-user reviews have been completed.

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Mesh:

Year:  2015        PMID: 25565585     DOI: 10.1097/AJP.0000000000000195

Source DB:  PubMed          Journal:  Clin J Pain        ISSN: 0749-8047            Impact factor:   3.442


  10 in total

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Review 2.  What is the future of patient-reported outcomes in sickle-cell disease?

Authors:  Sharon A Singh; Nitya Bakshi; Prashant Mahajan; Claudia R Morris
Journal:  Expert Rev Hematol       Date:  2020-10-15       Impact factor: 2.929

3.  Randomized clinical trial of computerized PAINRelieveIt® for patients with sickle cell disease: PAINReportIt® and PAINUCope®.

Authors:  Brenda W Dyal; Miriam O Ezenwa; Yingwei Yao; Robert E Molokie; Zaijie J Wang; Samir K Ballas; Marie L Suarez; Diana J Wilkie
Journal:  Patient Educ Couns       Date:  2019-08-17

4.  Evaluation of Longitudinal Pain Study in Sickle Cell Disease (ELIPSIS) by patient-reported outcomes, actigraphy, and biomarkers.

Authors:  Debra D Pittman; Patrick C Hines; David Beidler; Denis Rybin; Andrew L Frelinger; Alan D Michelson; Ke Liu; Xiufeng Gao; Jennell White; Ahmar U Zaidi; Robert J Charnigo; Michael U Callaghan
Journal:  Blood       Date:  2021-04-15       Impact factor: 22.113

5.  Availability of researcher-led eHealth tools for pain assessment and management: barriers, facilitators, costs, and design.

Authors:  Kristen S Higgins; Perri R Tutelman; Christine T Chambers; Holly O Witteman; Melanie Barwick; Penny Corkum; Doris Grant; Jennifer N Stinson; Chitra Lalloo; Sue Robins; Rita Orji; Isabel Jordan
Journal:  Pain Rep       Date:  2018-09-11

6.  Pain experiences of adults with osteogenesis imperfecta: An integrative review.

Authors:  Tracy Nghiem; Khadidja Chougui; Alisha Michalovic; Chitra Lalloo; Jennifer Stinson; Marie-Elaine Lafrance; Telma Palomo; Noémi Dahan-Oliel; Argerie Tsimicalis
Journal:  Can J Pain       Date:  2018-01-30

7.  Sickle Cell Transplantation Evaluation of Long-term and Late Effects Registry (STELLAR) to Compare Long-term Outcomes After Hematopoietic Cell Transplantation to Those in Siblings Without Sickle Cell Disease and in Nontransplanted Individuals With Sickle Cell Disease: Design and Feasibility Study.

Authors:  Lakshmanan Krishnamurti; Staci D Arnold; Ann Haight; Allistair Abraham; Gregory Mt Guilcher; Tami John; Nitya Bakshi; Shalini Shenoy; Karen Syrjala; Paul L Martin; Sonali Chaudhury; Gretchen Eames; Olusola Festus Olowoselu; Matthew Hsieh; Josu De La Fuente; Kimberly A Kasow; Elizabeth Stenger; Anne Mertens; Fuad El-Rassi; Peter Lane; Bronwen E Shaw; Lillian Meacham; David Archer
Journal:  JMIR Res Protoc       Date:  2022-07-06

8.  Validation of patient-reported vaso-occlusive crisis day as an endpoint in sickle cell disease studies.

Authors:  Karin S Coyne; Brooke M Currie; Michael Callaghan; Kathleen W Wyrwich; Sheryl Pease; Christine L Baker; Steven Arkin; Debra D Pittman
Journal:  Eur J Haematol       Date:  2022-06-20       Impact factor: 3.674

9.  Association of genetic variation in COMT gene with pain related to sickle cell disease in patients from the walk-PHaSST study.

Authors:  Yingze Zhang; Inna Belfer; Mehdi Nouraie; Qilu Zeng; Ruchika Goel; Yanxia Chu; Inna Krasiy; Lakshmanan Krishnamurti
Journal:  J Pain Res       Date:  2018-03-12       Impact factor: 3.133

10.  Effects of Music Therapy on Quality of Life in Adults with Sickle Cell Disease (MUSIQOLS): A Mixed Methods Feasibility Study.

Authors:  Samuel N Rodgers-Melnick; Lucas Lin; Kristina Gam; Evanilda Souza de Santana Carvalho; Coretta Jenerette; Douglas Y Rowland; Jane A Little; Jeffery A Dusek; Nitya Bakshi; Lakshmanan Krishnamurti
Journal:  J Pain Res       Date:  2022-01-11       Impact factor: 3.133

  10 in total

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