Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2022 | 2 |
2023 | 1 |
2024 | 1 |
Search Results
3 results
Results by year
Filters applied: . Clear all
Page 1
Best Practice Recommendations: User Acceptance Testing for Systems Designed to Collect Clinical Outcome Assessment Data Electronically.
Ther Innov Regul Sci. 2022 May;56(3):442-453. doi: 10.1007/s43441-021-00363-z. Epub 2022 Mar 1.
Ther Innov Regul Sci. 2022.
PMID: 35233726
Free PMC article.
Implementing clinical outcome assessments electronically in clinical studies requires the sponsor and electronic clinical outcome assessment (eCOA) provider to work closely together to implement study-specific requirements and ensure consensus-defined best practices …
Implementing clinical outcome assessments electronically in clinical studies requires the sponsor and electronic clinical outc …
Flexible approaches to eCOA administration in clinical trials: The site perspective.
Haenel E, Elash CA, Garner K, Turner M, Kern S; Electronic Clinical Outcome Assessment (eCOA) Consortium and the Patient-Reported Outcome (PRO) Consortium.
Haenel E, et al.
Contemp Clin Trials Commun. 2023 Dec 7;37:101241. doi: 10.1016/j.conctc.2023.101241. eCollection 2024 Feb.
Contemp Clin Trials Commun. 2023.
PMID: 38174210
Free PMC article.
The project aimed to identify clinical trial stakeholders' concerns related to electronic PRO (ePRO) implementation and propose areas of improvement via simplification and flexibility. ...A semi-structured questionnaire was developed and distributed via snowball sam …
The project aimed to identify clinical trial stakeholders' concerns related to electronic PRO (ePRO) implementation and propos …
Item in Clipboard
Comparability of a provisioned device versus bring your own device for completion of patient-reported outcome measures by participants with chronic obstructive pulmonary disease: qualitative interview findings.
Newton L, Knight-West O, Eremenco S, Hudgens S, Crescioni M, Symonds T, Reasner DS, Byrom B, O'Donohoe P, Vallow S; Patient-Reported Outcome (PRO) Consortium; Electronic Clinical Outcome Assessment (eCOA) Consortium.
Newton L, et al.
J Patient Rep Outcomes. 2022 Aug 4;6(1):86. doi: 10.1186/s41687-022-00492-5.
J Patient Rep Outcomes. 2022.
PMID: 35925498
Free PMC article.
BACKGROUND: There is interest in participants using their own smartphones or tablets ("bring your own device"; BYOD) to complete patient-reported outcome (PRO) measures in clinical studies. Our study aimed to qualitatively evaluate participants' experience using a p …
BACKGROUND: There is interest in participants using their own smartphones or tablets ("bring your own device"; BYOD) to complete patient …
Item in Clipboard
Cite
Cite