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Clinical Trials/NCT04883684
NCT04883684CompletedNot Applicable

A Multi-institutional Study to Evaluate Patient Satisfaction of the Personal Health Record Management Platform for Chronic Patients in Emergency Department Based on Actual Demand

Samsung Medical Center1 site in 1 country57 target enrollmentStarted: September 6, 2021Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
57
Locations
1
Primary Endpoint
SUS(System Usability Scale)-based assessment of patients or care givers satisfaction using personal health wallet service.

Study Overview

Brief Summary

The investigators developed the service showing patient health record altogether which is managed by each hospital separately and recording the patient health information based on mobile application. This study is a multi-centered study involving two hospitals, providing services to patients, care givers and medical staffs. After the participants use this service, the investigators evaluate the effectiveness and satisfaction of this service through questionnaires and in-depth interviews.

Detailed Description

<Background> Emergency situations for chronic patients are increasing due to aging, eating habits and lifestyle changes. For chronic patients, comprehensive health records and utilization are important for health care and emergency situations. In particular, in the event of an emergency, information on the patient's personal health records, such as recent surgery records, disease history, prescription and dosage history is needed immediately, but it is difficult to check separately for each hospital. In addition, in emergencies, it may take more time for proper treatment to take place if patients themselves cannot directly talk about their medication or past surgical history, or if they are unable to communicate with patients. Recently, conditions have been prepared for the collection and utilization of personal health record information due to changes in policy and technology environment, making it possible to provide services for emergency patients with chronic diseases.

<Objective> To establish a service for collection and utilization of medical records (care, examination, surgery, prescription records) and PGHD for chronic patients and to evaluate its effectiveness.

<Design> Mixed methods study (questionnaires and interview)

<Setting> At the Samsung Medical Center and the Dong-A Medical Center.

<Enrollment> 400 patients(care givers)

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
19 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •\ * A chronic patient (or his or her care giver) who visits the emergency department and has a plan to visit outpatient or other hospitals in one month of the visiting emergency department.
  • •* Adults over 19 years old.
  • •* Those who voluntarily agreed to participate in the research

Exclusion Criteria

  • •Anyone who disagrees with this study
  • •Patients who are not conscious when leaving the emergency room, patients who are not aware of or are not aware of their orientation, patients who are not aware of their level of awareness, or people who are in shock or in deep shutdown situations) (Even in the above cases, caregivers can be included in the clinical trial target if they are present. )

Arms & Interventions

Patients(Care givers)

Experimental
  1. 400 patients(caregivers) are enrolled and use the personal health wallet service (Personal Health Records service).
  2. They fill out questionnaire to evaluate the service
  3. Some of them are invited for an in-depth interview.

Intervention: Personal health wallet service for Chronic Patients in Emergency Department (Other)

Outcomes

Primary Outcomes

SUS(System Usability Scale)-based assessment of patients or care givers satisfaction using personal health wallet service.

Time Frame: 8 weeks after the enrollment

SUS(System Usability Scale)-based assessment of patients or care givers satisfaction using personal health wallet service. SUS consists of a 10 item questionnaire with five response options for respondents; from Strongly agree to Strongly disagree. Its score range is 0\~100 and the higher the score, the higher the satisfaction level.

SUS(System Usability Scale)-based assessment of patients or care givers satisfaction using personal health wallet service.

Time Frame: The day of the enrollment of the study

SUS(System Usability Scale)-based assessment of patients or care givers satisfaction using personal health wallet service. SUS consists of a 10 item questionnaire with five response options for respondents; from Strongly agree to Strongly disagree. Its score range is 0\~100 and the higher the score, the higher the satisfaction level.

SUS(System Usability Scale)-based assessment of patients or care givers satisfaction using personal health wallet service.

Time Frame: 2 weeks after the enrollment

SUS(System Usability Scale)-based assessment of patients or care givers satisfaction using personal health wallet service. SUS consists of a 10 item questionnaire with five response options for respondents; from Strongly agree to Strongly disagree. Its score range is 0\~100 and the higher the score, the higher the satisfaction level.

SUS(System Usability Scale)-based assessment of patients or care givers satisfaction using personal health wallet service.

Time Frame: 4 weeks after the enrollment

SUS(System Usability Scale)-based assessment of patients or care givers satisfaction using personal health wallet service. SUS consists of a 10 item questionnaire with five response options for respondents; from Strongly agree to Strongly disagree. Its score range is 0\~100 and the higher the score, the higher the satisfaction level.

Secondary Outcomes

  • A quantitative or qualitative study on the log data of the application(through study completion, an average of 3 months")
  • A qualitative study on the satisfaction of patients or care givers through interviews(through study completion, an average of 3 months")

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Taerim Kim

Clinical Assistant Professor

Samsung Medical Center

Study Sites (1)

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