Subjects with osteoarthritis can easily use a handheld touch screen electronic device to report medication use: qualitative results from a usability study

被引:8
|
作者
Khurana, Laura [1 ]
Durand, Ellen M. [1 ]
Gary, Sarah T. [1 ]
Otero, Antonio V. [1 ]
Gerzon, Millie C. [1 ]
Beck, Jamie [1 ]
Hall, Chris [1 ]
Dallabrida, Susan M. [1 ]
机构
[1] eRes Technol Inc, 500 Rutherford Ave, Boston, MA 02129 USA
来源
PATIENT PREFERENCE AND ADHERENCE | 2016年 / 10卷
关键词
ePRO; patient preference; eDiary; usability testing; CLINICAL-TRIALS; KNEE OSTEOARTHRITIS; OUTCOME MEASURES; TOTAL HIP; PATIENT; PAPER; EQUIVALENCE; RECOMMENDATIONS; ARTHRITIS; IMPACT;
D O I
10.2147/PPA.S94247
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: Electronic data capture is increasingly used to improve collection of patient-reported outcome measures in clinical trials and care. The validation of electronic patient-reported outcome devices requires information on patient preference and ease of use. This study conducted usability testing for a General Symptom Questionnaire and Medication Module (TM) on a handheld device for subjects with osteoarthritis (OA) to determine whether subjects can report on their symptoms and medication use using an electronic diary. Methods: Nine subjects with OA participating in a large US mode equivalency study were surveyed independently in this study. Subjects completed a General Symptom Questionnaire and Medication Module T using the LogPad (R) LW handheld device. Demographic and technology use information was collected, and the subjects were queried on device usability. Results: Subjects reported that the handheld device was easy to use and that they were able to complete a General Symptom Questionnaire and Medication Module T with little or no assistance. They did not report any issues with the screen or size of the device. Subjects were willing to travel with the device to complete electronic diaries at home or in public. Participants indicated that they would be able to use the handheld device to answer questions during a clinical trial. Subjects with OA experienced no physical discomfort during completion of either questionnaire. Conclusion: The General Symptom Questionnaire and Medication Module T were usable and acceptable to subjects with OA on a handheld device. This was consistent regardless of previous experience and confidence with technology, despite the potential physical restrictions for an OA cohort.
引用
收藏
页码:2171 / 2179
页数:9
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