Skip to content

The Efficacy of Electrical Version of Patient Reported Outcome

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02387073
Enrollment
100
Registered
2015-03-12
Start date
2013-09-30
Completion date
2014-03-31
Last updated
2015-07-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Spinal Disease

Keywords

outcome assessment, self-reported, patient, clinical outcome

Brief 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.

Detailed description

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

Interventions

OTHERElectrical version patient reported outcome questionnaire

Assess satisfaction of patients with electrical version patient reported outcome questionnaire.

Sponsors

SK Telecom Consortium
CollaboratorOTHER
Seoul National University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
15 Years to 80 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
The necessity of electrical PRO system (quantitative analysis)up to 6 months after introduction of e-PRO systemDo you feel the e-PRO system is necessary? 1. Absolutely yes 2. Yes 3. No 4. Absolutely no

Secondary

MeasureTime frameDescription
Consultation efficacy with doctor Satisfaction for the enough exchange of informationup to 6 months after introduction of e-PRO systemDo you feel the e-PRO system make the consultation time with doctor to be efficient? 1. Absolutely yes 2. Yes 3. No 4. Absolutely no Do you think your status was expressed better with the use of e-PRO 1. Absolutely yes 2. Yes 3. No 4. Absolutely no

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026