Skip to content

Korean Medicine Patient Registry of Postoperative Therapy for Musculoskeletal Disorders (KPOP-MD): A Study Protocol

Korean Medicine Patient Registry of Postoperative Therapy for Musculoskeletal Disorders (KPOP-MD): A Study Protocol

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03842098
Enrollment
150
Registered
2019-02-15
Start date
2019-06-01
Completion date
2022-05-31
Last updated
2021-10-15

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

Conditions

Korean Medicine Patient Registry, Musculoskeletal Disorders, Post-operative Therapy

Keywords

Korean Medicine Patient Registry, Post-operative Therapy, Musculoskeletal Disorders

Brief summary

To create an infrastructure that allows for the conduct of prospective, controlled studies comparing the effectiveness of diagnostic and treatment strategies for patients with musculoskeletal disorders after musculoskeletal operations

Interventions

None listed

Sponsors

Kyunghee University Medical Center
CollaboratorOTHER
CHUNG YEON Korean Medicine Hospital
CollaboratorUNKNOWN
Korean medicine hospital of Daejeon University
CollaboratorUNKNOWN
Wonkwang University Iksan Korean Medicine Hospital
CollaboratorUNKNOWN
Gachon University Gil Oriental Medical Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* aged 19 and over * Those who have undergone musculoskeletal related surgery (corresponding to the disease classification code M00-99, S00-99) within 3 years * voluntary applicant who has no problem with communicate with study associates or a mild cognitive impairment patient who scored higher than 23 points in Korean version of the montreal rating questionnaire with voluntary participation

Exclusion criteria

* Participants in other clinical trials * Those who are unlikely to be adhered to the schedule of clinical studies * Those who are expected to have difficulty understanding and responding to research questionnaires such as illiteracy, mental and physical weakness

Design outcomes

Primary

MeasureTime frameDescription
Change in musculoskeletal pain intensityAt baseline, enrollment after 3/6/9/12 monthsAssessment of musculoskeletal pain intensity by Numeric Rating Scale (NRS)
Change in Disability and estimating quality of lifeAt baseline, enrollment after 3/6/9/12 monthsDisability and estimating quality of life by Oswestry Disability Index
Change in reduction of pain severity by K-WOMACAt baseline, enrollment after 3/6/9/12 monthsAssessment of pain severity by K-WOMAC
Change in Pain and disability of the shoulder by SPADI questionnaireAt baseline, enrollment after 3/6/9/12 monthsAssessment of Pain and disability of the shoulder by SPADI questionnaire
Change in current health statusAt baseline, enrollment after 3/6/9/12 monthsThe health status will be observed with the Euroqol (EQ-5D-5L) questionnaire.
Change in Severity assessment of any symptoms other than painAt baseline, enrollment after 3/6/9/12 monthsSeverity assessment of any symptoms other than pain by Numeric Rating Scale (NRS)

Countries

South Korea

Contacts

Primary ContactYoume Ko, MA
meyougo@khu.ac.kr8229619278

Outcome results

None listed

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