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A Prospective Total Joint Surgery Registry to Monitor Short- and Long-Term Clinical Outcomes

A Prospective Total Joint Surgery Registry to Monitor Short- and Long-Term Clinical Outcomes

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06687109
Enrollment
10000
Registered
2024-11-13
Start date
2020-01-10
Completion date
2030-01-01
Last updated
2026-04-29

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

Conditions

Osteoarthritis

Brief summary

The investigators propose a prospective longitudinal registry study to collect and compare preoperative and postoperative information from patients who undergo total joint arthroplasty (TJA). Outcomes will be assessed with common, routinely available patient-reported outcomes measures (PROM's) such as the HOOS Jr., Oxford score, Knee Society Score, Harris Hip Score, and other patient satisfaction and function assessments in use in Orthopedics.

Detailed description

The investigators propose a prospective longitudinal registry study to collect and compare preoperative and postoperative information from patients who undergo total joint arthroplasty (TJA). Outcomes will be assessed with common, routinely available patient-reported outcomes measures (PROM's) such as the HOOS Jr., Oxford score, Knee Society Score, Harris Hip Score, and other patient satisfaction and function assessments in use in Orthopedics. Investigators will also record both demographic and clinical data about the subject's history of joint pain, past treatment, medical co-morbidities, and surgical procedure. Additionally, gait analysis and standardized physical capacity testing will be included as an option. All patients undergoing hip or knee replacement with the primary investigator will be included for data collection. All procedures and treatment will follow the standard of care, and all prosthetic implants with be FDA-approved. Data will be used to evaluate the effect on both short and long-term comfort and function of patients diagnosed with hip or knee pain who undergo joint replacement. The main purpose of the study is to provide quality improvement data on the patients in the Principal Investigator's (PI's) practice currently undergoing joint surgery. This project creates a data repository to store participants' data for this and possible future research.

Interventions

PROCEDURETotal Knee Arthroplasty

Total Knee Arthroplasty

PROCEDURETotal Hip Arthroplasty

Total Hip Arthroplasty

Sponsors

Spokane Joint Replacement Center
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Patients who are scheduled to undergo TJA by the Principal Investigator

Exclusion criteria

* Age \< 18 * Unable to speak and read English * Prisoners or any other patients who, in the opinion of the investigator, are unlikely to return for follow-ups or unreliable in completing the assessments

Design outcomes

Primary

MeasureTime frameDescription
Knee Society ScorePre-op, 6 weeks, 6 months, 1 year, 2 years, and 5 yearsThe Knee Society Score (KSS) provides a 0 to 100 score measuring function, pain, and range of motion in the knee before and after surgery. A score of 0 indicates the worst outcome, while a score of 100 indicates the best outcome.
Forgotten Joint ScorePre-op, 6 weeks, 6 months, 1 year, 2 years, and 5 yearsThe Forgotten Joint Score assesses how aware the patient is of their joint in everyday life. A score of 0 is the worst (always aware) while a score of 100 is the best (the patient is so comfortable, they forget that the joint was replaced).
Joint Awareness SurveyPre-op, 6 weeks, 6 months, 1 year, 2 years, and 5 yearsThe Joint Awareness Survey is an abbreviated version of the Forgotten Joint Score. It also has 0 as the worst outcome and 100 as the best. We are including it to determine if it can reliably be used in place of the Forgotten Joint Score, which is longer and more burdensome for patients to fill out.
Pain Satisfaction ExpectationsPre-op, 6 weeks, 6 months, 1 year, 2 years, and 5 yearsThis survey assesses patients' satisfaction with their joint, their pain level, their overall function, and their need for pain medication. 0 is the worst score while 100 is the best.
PROMIS Global HealthPre-op, 6 weeks, 6 months, 1 year, 2 years, and 5 yearsThis survey assesses the general health and quality of life of the patient. It is also a 0-100 point scale with 100 being best, 0 being worst, and 50 being average. Every 10 points represents one standard deviation from the mean.
Koos Jr. Knee SurveyPre-op, 6 weeks, 6 months, 1 year, 2 years, and 5 yearsThis survey assesses stiffness, pain, and function of the knee. 0 is the worst score and 100 is the best.
Harris HipPre-op, 6 weeks, 6 months, 1 year, 2 years, and 5 yearsThis survey assesses pain, deformity, and range of motion of the hip. A score of 0 indicates the worst outcome and 100 indicates the best.
Hoos Jr.Pre-op, 6 weeks, 6 months, 1 year, 2 years, and 5 yearsThis survey assesses pain and function of the hip in daily life. A score of 0 indicates the worst outcome, while a score of 100 indicates the best.

Countries

United States

Contacts

CONTACTDavid F Scott, MD
dfscott@mac.com509-466-6393
CONTACTAnnalise R McInelly, MPH
Annalise@orthospecialtyclinic.com509-466-6393
PRINCIPAL_INVESTIGATORDavid Scott, MD

Spokane Joint Replacement Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 30, 2026