Economic and Functional Impact of Peri-Operative Bracing for Primary Total Knee Arthroplasty (TKA)
To Determine the Economic and Functional Impact of Peri-Operative Extension Assist Pneumatic Bracing for Primary Total Knee Arthroplasty (TKA) Non-Inferiority Trial
Panoramica dello studio
Stato
Stato
Condizioni
Condizioni
Intervento / Trattamento
Intervento / Trattamento
Tipo di studio
Tipo di studio
Iscrizione (Effettivo)
Iscrizione
Fase
Fase
- Non applicabile
Contatti e Sedi
Luoghi di studio
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Ohio
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Cleveland, Ohio, Stati Uniti, 44195
- Cleveland Clinic
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Criteri di partecipazione
Criteri di ammissibilità
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
Age: 50 years or older
Exclusion Criteria:
- BMI > 40
- Radiographic deformity of greater than 10 degrees
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Separare
Numero di armi
Armi e interventi
Gruppo di partecipanti / ArmGruppo di partecipanti / Arm |
Intervento / TrattamentoIntervento / Trattamento |
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Nessun intervento: Control group
Subjects will receive two out-patient physical therapy (PT) visits per week for 2 weeks, followed by additional PT visits at clinician's discretion after TKA.
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Sperimentale: Bracing group
Subjects will be fitted with the Ongoing Care Solutions, Inc (OCSI) Rehabilitator brace prior to surgery.
This brace will be worn for 6 weeks before surgery.
The brace will be worn again after surgery ~10 days after surgery or when staples are removed until the end of the study.
Participants will also have two PT visits per week for 2 weeks, followed by additional PT visits at clinician's discretion.
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Guardian Brace features the innovative Rehabilitator™ line of gait correcting, leg strengthening braces.
Rehabilitator™ Knee Braces are clinically proven to reduce UNBRACED pain, strengthen the affected leg, and significantly improve function after only 90 days of brace wear.
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Number of Physical Therapy Visits
Lasso di tempo: Total number of visits from date of surgery to 12 weeks after surgery
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Investigators will monitor the total number of physical therapy visits that was necessary to return to normal function between the control and bracing group and how it relates to overall cost.
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Total number of visits from date of surgery to 12 weeks after surgery
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Misure di risultato secondarie
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Visual Analog Scale (VAS) for Pain (0-10 Scale)
Lasso di tempo: Change from baseline to 12 weeks after surgery
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Visual Analog Scale is a a pain scale assessment instrument that has been widely used to allow adult patients to report their pain level in musculoskeletal research studies.
It is a continuous scale comprised of a horizontal line, 10 centimeters (100 mm) in length, anchored by 2 two ends representing the extremes of measurements with 0 point representing no pain and 10 representing the worst pain a patient may have had.
Therefore, starting from zero point, increasing numbers demonstrate worse pain.
Patient can pick a point on the scale that they believe represent their pain level at a given moment.
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Change from baseline to 12 weeks after surgery
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Timed up and go Test (Timed Measurement)
Lasso di tempo: Change from baseline to 12 weeks after surgery
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Used to assess a person's mobility and balance.
It is measured in time units (seconds or minutes) using a stopwatch by a study personnel.
To perform, the patient sits back in a standard arm chair and a line 3 meters, or 10 feet away on the floor is identified.
At the investigator mark, the stopwatch is started and the patient is asked to stand up from chair, walk to the end of the line and come back to his chair at normal pace.
The results is the time in seconds needed for the patient to perform the test (getting up from chair and coming back to it as timed by the investigator's stopwatch)
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Change from baseline to 12 weeks after surgery
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Timed Stair Climb (Timed Measurement Over Fixed Distance)
Lasso di tempo: Change from baseline to 12 weeks after surgery
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Used to assess a person's mobility and balance
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Change from baseline to 12 weeks after surgery
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One-leg Stance Time (Timed Measurement)
Lasso di tempo: Change from baseline to 12 weeks after surgery
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Used to assess a person's balance.
Performed with eyes open and arms on hips.
The patient is asked to stand unassisted on one leg and is timed in seconds (using stopwatch) from the time one foot is flexed off the floor to the time when it touches the ground or the standing leg or an arm leaves the hips.
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Change from baseline to 12 weeks after surgery
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6 Minute Walk Test (Distance Measurement)
Lasso di tempo: Change from baseline to 12 weeks after surgery
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Used to assess a person's endurance and aerobic capacity.
The score of the test is distance a patient walks in 6 minutes.
Longer distances walked by the patient in 6 minutes correlates with better performance.
Distance is measured using distance measuring wheel.
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Change from baseline to 12 weeks after surgery
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Knee Society Score Questionnaire
Lasso di tempo: Change from baseline to 12 weeks after surgery
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Clinical outcome questionnaire developed by the consensus of the Knee Society.
It comprises, a "Knee score" and a "Functional score."
The Knee score assesses pain, stability, and range of motion.
A maximum score of 100 is achieved by a painless, well-aligned knee with 125° range of motion, with neither anteroposterior nor mediolateral instability.
Deductions are made for flexion contracture, extension lag, and malalignment.
The Functional score assesses walking distance and stair climbing.
A maximum score of 100 is assigned to individuals who can walk unlimited distances and can climb up and down stairs normally.
Deductions are made for use of a walking stick or crutches.
Therefore, higher scores correlate with better function and outcome.
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Change from baseline to 12 weeks after surgery
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Knee Injury and Osteoarthritis Outcome Score Jr. (KOOS Jr.) Questionnaires
Lasso di tempo: Change from baseline to 12 weeks after surgery
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Clinical outcome questionnaire that measure joint-specific pain and physical function.
It has seven questions that focus on three categories: joint pain, stiffness, and function, in daily living.
Raw scores are added up (range 0-28) and converted to an interval score (0-100) using an interval table.
The interval score represents a patients total joint disability where 0 corresponds to total joint disability and 100 perfect joint health.
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Change from baseline to 12 weeks after surgery
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Hospital for Special Surgery (HSS) Score (0-100 Scale)
Lasso di tempo: Change from baseline to 12 weeks after surgery
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Clinical outcome assessment tool.
It is based on a total of 100 points.
The score is divided into seven categories, which include pain, function, range of motion, muscle strength, flexion deformity, instability, and subtractions.
The knee is initially given a score of 0, and additions or subtractions are made according to specific criteria.
The higher the score, the better the outcome.
Approximately 50% of the score is based on a patient interview and the remaining on physical exam.
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Change from baseline to 12 weeks after surgery
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Type of Pain Medication Used
Lasso di tempo: Change from baseline to 12 weeks after surgery
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Investigators will monitor the medical record for types of pain medications used.
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Change from baseline to 12 weeks after surgery
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Amount of Pain Medication Used
Lasso di tempo: Change from baseline to 12 weeks after surgery
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Investigators will monitor the medical record for the amount of pain medication used
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Change from baseline to 12 weeks after surgery
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Collaboratori e investigatori
Sponsor
Sponsor
Investigatori
Investigatori
- Cattedra di studio: Spindler Kurt, MD, Department Chair
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Inizio studio
Completamento primario (Effettivo)
Completamento primario
Completamento dello studio (Effettivo)
Completamento dello studio
Date di iscrizione allo studio
Primo inviato
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Primo Inserito
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento pubblicato
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
Altri numeri di identificazione dello studio
- SHB-OCSI007
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