Healthy Clinical Trial
— CePROOfficial title:
Usability and Satisfaction With an Electronic Survey Administration Application in General Population
The goal of the study is to assess the usability and satisfaction of an electronic patient reported outcomes (e-PRO) mobile application. The secondary aim is to assess and compare response rates between two study groups (e-PRO group vs REDCap survey group). A potential differentiating factor between delivering surveys via smart phone and other electronic modes of delivery is the perceived advantage of being able to conveniently complete survey questionnaires at any time and any location. This could help address certain limitations of the quantitative survey method such as recall bias. Furthermore, the portability, connectivity and ubiquity of smartphones may reduce the amount of training or instructions required for users to complete a survey questionnaire on a smartphone.
Status | Not yet recruiting |
Enrollment | 30 |
Est. completion date | February 28, 2020 |
Est. primary completion date | January 30, 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Healthy participants over the age of 18-65 years as assessed by the Self-Rated Health Measure. - Fluency in English language to be able to read, understand study procedures and complete surveys administered during the study. - Willing to travel to the downtown Boston area to participate in up to two study visits. - Willing to participate in the research study and sign informed consent. Exclusion Criteria: - Participants with a "fair" or "poor" rating on the Self-Rated Health Measure. - Participants with EU citizenship or permanent residency - Participants with severe cognitive, vision, hearing, or speech problems that may prevent them from answering surveys - Participants with serious psychiatric conditions (moderate or major depressive disorder that may impair their ability to complete surveys - Participants with any terminal illness (e.g. cancers) - Patients with implantable devices, pacemakers or body worn electronic medical devices |
Country | Name | City | State |
---|---|---|---|
United States | Partners Healthcare | Boston | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
Massachusetts General Hospital | Cenduit LLC |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Usability of e-PRO vs. emailed link: survey | A survey will be administered to compare groups on their experiences with the survey-method administration (Investigator developed survey). The following components will be taken into account: acceptability-- participant satisfaction with various aspects of the solution (e.g. content, complexity, comfort, delivery, and credibility). Adoption-- participants' intention to try; perceived barriers and facilitators for uptake. Appropriateness-- participant's perceived relevance to need; suitability to daily patient workflow. Feasibility-- suitability for using daily, weekly etc. This survey is not a scored survey. | At close-out | |
Secondary | Survey response rate e-PRO vs emailed link | Response rate will be tracked on a weekly basis from the e-PRO system and the REDCap embedded email link to compare response rate between the control and intervention group. The AAOPR (2006) recommendation for RR formula will be used to calculate the RR. This is the number of completed surveys (completed and partially completed) divided by the number of completed surveys (completed and partially completed) plus the number of all non-completed surveys (sent to a potential participant but not completed because of incorrect e-mail address, incorrect mailing address, or other reasons). | At close-out |
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