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Functional Recovery After Total Knee Arthroplasty

19 de febrero de 2018 actualizado por: Mahidol University

The Evaluation of Short-term Functional Recovery of Total Knee Arthroplasty Patients

Total knee replacement is one of the most successful surgical procedures in Orthopaedics. However, 10-20% of the patients are still dissatisfied with the results of the surgery. In general, the evaluation of postoperative functional outcomes are usually measured by self-report questionnaires, such as the Western Ontario and Mcmaster Universities osteoarthritic Index (WOMAC) and the Short Form-36 health survey (SF-36). Another method to evaluate functional outcome of the patients is to use the performance-based tests such as the two-minute walk test, but there is still little information regarding its use for evaluating functional recovery in patients receiving total knee arthroplasty.

The objectives this study are: 1) to assess the relationship between self-report questionnaires and performance-based tests among patients scheduling for TKA; and 2) to identify clinical variables that are associated with pre- and postoperative functional performance of the patients.

Descripción general del estudio

Estado

Terminado

Intervención / Tratamiento

Descripción detallada

Osteoarthritis (OA) of the knee is one of the most prevalent age-related musculoskeletal conditions, resulting in significant impairment in patients' abilities to perform activities and adversely impacting their quality of life. The level of impairment in patients with knee OA can be measured using validated self-report questionnaires, such as the disease-specific Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) and the generic Medical Outcomes Study Short Form-36 (SF-36). Self-report questionnaires have been recommended by some investigators for their high internal consistency and ease of administration. Another method to evaluate physical function in patients with knee OA is to use performance-based tests. These tests are tools that assess patients' ability to execute a task in a standardized environment, and include the 2-minute walk test (2MWT) and the timed get-up-and-go test (TUG).

Among all the self-reported questionnaires for knee OA, the WOMAC is one of the most commonly used for baseline assessment and for measurement of treatment outcome, and has been validated for patients undergoing total knee arthroplasty (TKA). Although the WOMAC provides information on how individuals perceive their physical function in their own environment, it does not describe their ability to perform a specific task or action. In addition, some investigators showed that scores from self-report questionnaires before and after arthroplasty can overestimate patients' actual functional capacity. For example, Parent et al demonstrated that total knee arthroplasty patients had a dramatic improvement at 2 months as assessed by the WOMAC function subscale, however there were no significant changes when measured with performance-based tests assessing gait speed and stair ascent duration. Therefore, clinicians should be cautious when interpreting findings from studies that provide only self-report questionnaire scores. Given that self-report questionnaires may over-estimate functional status after joint replacement, some authors advocate performance-based tests as measures of outcome, and recommend their use during the preoperative period as baseline measurements followed by subsequent comparison with postoperative measurements.

The objectives of this study are: 1) to assess the relationship between self-reported questionnaires (WOMAC and SF-36) and performance-based tests (2MWT, TUG) among patients scheduling for TKA; and 2) to identify clinical variables that are associated with pre- and post-operative performance of the 2MWT and TUG. Our hypothesis is that correlations between self-report questionnaires and performance-based tests would be low to moderate, and thus these two types of measurements evaluate distinct domains of functional status in patients undergoing TKA.

Tipo de estudio

De observación

Inscripción (Actual)

80

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

    • Bangkok
      • Bangkoknoi, Bangkok, Tailandia, 10700
        • Siriraj Hospital

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

40 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Método de muestreo

Muestra no probabilística

Población de estudio

Patients who receive uncomplicated total knee replacement by a single surgeon

Descripción

Inclusion Criteria:

  • Patients who aged between 40-100 years
  • Patients who diagnosed with end-stage osteoarthritis of the knee

Exclusion Criteria:

  • Patients who receive total knee replacement on the contralateral side during the past 6 months
  • Patients with diseases or conditions that may affect postoperative functional recovery such as severe cardiopulmonary disease
  • Unable to participate in postoperative follow-up visits
  • Prior surgery on the affected knee, such as high tibial osteotomy
  • Patients with complex deformity who require bone grafting or metal augments

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

Cohortes e Intervenciones

Grupo / Cohorte
Intervención / Tratamiento
Total knee arthroplasty
Patients undergoing uncomplicated total knee replacement
All patients will undergo total knee replacement using midvastus approach by single surgeon.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Periodo de tiempo
Change of the 2-minute walk test (2MWT) from baseline to at 1 year after surgery
Periodo de tiempo: baseline, 6 weeks, 3 months, 6 months and 1 year after surgery
baseline, 6 weeks, 3 months, 6 months and 1 year after surgery

Medidas de resultado secundarias

Medida de resultado
Periodo de tiempo
Change of the Timed get-up-and-go test (TUG) from baseline to 1 year after surgery
Periodo de tiempo: baseline, 6 weeks, 3 months, 6 months and 1 year after surgery
baseline, 6 weeks, 3 months, 6 months and 1 year after surgery
Change of the pain scores on the Visual Analog Scale from baseline to 1 year after surgery
Periodo de tiempo: baseline, 6 weeks, 3 months, 6 months and 1 year after surgery
baseline, 6 weeks, 3 months, 6 months and 1 year after surgery
Change of the functional scores on the WOMAC index (Thai version) from baseline to 1 year after surgery
Periodo de tiempo: baseline, 3 months, 6 months and 1 year after surgery
baseline, 3 months, 6 months and 1 year after surgery
Change of the physical function domain of the SF-36 Health Survey from baseline to 1 year after surgery
Periodo de tiempo: baseline, 3 months, 6 months and 1 year after surgery
baseline, 3 months, 6 months and 1 year after surgery

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Investigadores

  • Investigador principal: Aasis Unnanuntana, M.D., Siriraj Hospital

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio

1 de mayo de 2013

Finalización primaria (Actual)

1 de febrero de 2018

Finalización del estudio (Actual)

1 de febrero de 2018

Fechas de registro del estudio

Enviado por primera vez

2 de junio de 2014

Primero enviado que cumplió con los criterios de control de calidad

3 de junio de 2014

Publicado por primera vez (Estimar)

5 de junio de 2014

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

22 de febrero de 2018

Última actualización enviada que cumplió con los criterios de control de calidad

19 de febrero de 2018

Última verificación

1 de febrero de 2018

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • 126/2556(EC2)

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

Ensayos clínicos sobre Total knee arthroplasty

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