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CompletedNCT02387073Updated Jul 8, 2015

The Efficacy of Electrical Version of Patient Reported Outcome

An observational study in Spinal Disease, sponsored by Seoul National University Hospital. Completed at 1 site in Korea, Republic of. Open to participants aged 15 Years to 80 Years. Per ClinicalTrials.gov, last updated 2015-07-08.

Sponsored by Seoul National University Hospital · Observational

Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
100
Ages
15 Years to 80 Years
Sex
All
01

Study 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.

Read the detailed description

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

02

Conditions studied

  • Spinal Disease

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Keywords

  • outcome assessment
  • self-reported
  • patient
  • clinical outcome
03

In context

Spinal Diseases

267 studies on the registry are indexed under Spinal Diseases; 54 are open to participants now.

This study's enrollment of 100 is close to the median of 108 across 87 observational studies indexed under Spinal Diseases.

Browse Spinal Diseases studies →

Lead sponsor

Seoul National University Hospital is the lead sponsor of 1,860 studies on the registry; 275 are open to participants now.

Of its 12 completed or terminated interventional studies of FDA-regulated products, 2 (17%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
15 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

the patients who have experienced paper questionnaire

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

Exclusion Criteria:

  • Computer illiterate
  • Uncooperative patient
05

Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
100 participants (actual)
Target follow-up
1 Month
Patient registry
Yes

Groups and cohorts

  • Electrical version

    Electrical version patient reported outcome questionnaire was used for patients who had filled-up same questionnaire in a paper version

    Other: Electrical version patient reported outcome questionnaire

Interventions

  • OtherElectrical version patient reported outcome questionnaire

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

    Also known as: Electrical patient reported outcome

06

What researchers measure

Primary outcomes

  1. The necessity of electrical PRO system (quantitative analysis)

    Do you feel the e-PRO system is necessary? 1. Absolutely yes 2. Yes 3. No 4. Absolutely no

    Time frame: up to 6 months after introduction of e-PRO system

Secondary outcomes

  1. 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? 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

    Time frame: up to 6 months after introduction of e-PRO system

07

Study locations

1 site
  • Seoul National University Hospital
    Seoul, 110-744, Korea, Republic of
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 8, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02387073
Lead sponsor
Seoul National University Hospital
Collaborators
SK Telecom Consortium
Responsible party
Chun Kee Chung (Professor, Seoul National University Hospital) — Principal investigator
First posted
Mar 12, 2015
Start date
Sep 2013
Primary completion
Mar 2014
Completion
Mar 2014
Last update
Jul 8, 2015

Study contacts

Chun Kee Chung, MD, PhD
principal investigator · Seoul National University Hospital

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2015. You cannot join it, but the record below documents what was studied.

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