The Efficacy of Electrical Version of Patient Reported Outcome

Spinal Disease Clinical Trial

Official title:

The Efficacy of Electrical Version of Patient Reported Outcome: Patient Survey

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02387073
• Other study ID #: E-PRO
• Secondary ID: H-1207-088-418
• Status: Completed
• Phase: N/A
• First received: November 29, 2013
• Last updated: July 6, 2015
• Start date: September 2013
• Est. completion date: March 2014

Study information

• Verified date: July 2015
• Source: Seoul National University Hospital
• Contact: n/a
• Is FDA regulated: No
• Health authority: Korea: Institutional Review Board
• Study type: Observational [Patient Registry]

Clinical Trial Summary

Recently the importance of electrical PRO system is increased for the accuracy, convenience, and efficiency for both patients and physicians. For the evaluation of quality of life, various self-reported questionnaires is filled-out by the patient, mostly in front of outpatient clinic, and doctor usually take times to calculate the score. If there is electrical PRO which is available with mobile device, the efficacy of clinic would be improved. The investigators developed such a system and applied the system for patients with spinal disease. The investigators assessed the effectiveness of application of electrical-PRO in outpatients' clinic for patients who had filled-up same questionnaire in paper version.

Description:

Age, sex, education levels, use of smartphone, the number of applications.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 100
• Est. completion date: March 2014
• Est. primary completion date: March 2014
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 15 Years to 80 Years

Eligibility

Inclusion Criteria:

• We assessed the effectiveness of application of electrical-PRO in outpatients' clinic for patients who had filled-up same questionnaire in paper version

Exclusion Criteria:

• Computer illiterate

• Uncooperative patient

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

• Spinal Disease
• Spinal Diseases

Intervention

Other:
• Electrical version patient reported outcome questionnaire
Assess satisfaction of patients with "electrical version patient reported outcome questionnaire".

Locations

Country	Name	City	State
Korea, Republic of	Seoul National University Hospital	Seoul

Sponsors (2)

Lead Sponsor	Collaborator
Seoul National University Hospital	SK Telecom Consortium

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The necessity of electrical PRO system (quantitative analysis)	Do you feel the e-PRO system is necessary?; Absolutely yes; Yes; Absolutely no	up to 6 months after introduction of e-PRO system	No
Secondary	Consultation efficacy with doctor Satisfaction for the enough exchange of information	Do you feel the e-PRO system make the consultation time with doctor to be efficient?; Absolutely yes; Yes; Absolutely no; Do you think your status was expressed better with the use of e-PRO; Absolutely yes; Yes; Absolutely no	up to 6 months after introduction of e-PRO system	No