- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT02806622
Comparison of Hip Range of Motion Values Among NCAA Division II Collegiate Athletes
Descripción general del estudio
Estado
Condiciones
Descripción detallada
Currently there is no normative data for hip passive ROM in apparently healthy NCAA division II collegiate athletes. This study will be the first study to develop preliminary normative data of hip passive ROM.
One hundred (N=100) student athletes (18-45 years) from California State University Dominguez Hills (CSUDH) will be recruited for this study via convenience sampling. Data collection will take place in the CSUDH sports medicine laboratory. Prior to testing, participants will fill out a screening questionnaire with questions that represent the exclusion criteria which will be used to determine ineligibility for this study.
Prior to participant recruitment and enrollment, a pilot study will be done on 10 participants to establish rater reliability using the methods mentioned below. After acceptable reliability is achieved, recruitment and enrollment will continue.
Participants who meet the inclusion criteria and consent to participate will be enrolled in the study. Participants will read and sign a CSUDH approved consent form prior to beginning data collection. Following consent, participants will also fill out a questionnaire to provide demographic information which includes age, height, weight, and leg dominance.
Following completion of the paperwork, all participants will undergo testing which will be conducted between the hours of 8am and 4pm. Each data collection session will last for approximately 20 minutes. Bilateral hip passive ROM data will be collected using the Noraxon computerized motion system. Participants will be lying in different positions on an examination table while the hip joints and lower extremities are moved into different positions and measured by the device which will touch the skin. Data will be collected and monitored by the examiner using the computerized system. The data collection protocol for both lower extremities are as follows:
- Supine measures (passive): hip external rotation, hip internal rotation
- Rest: 5-minute delay
- Seated measures (passive): hip external rotation, hip internal rotation
- Rest: 5-minute delay
- Prone measurements (passive): hip external rotation, hip internal rotation
Collected data will be transferred to SPSS v.22 (IBM SPSS, Chicago, IL). Means,standard deviations, 95% confidence intervals (95% CI), and ranges for participant descriptive data will be calculated. Passive Hip ROM values will be presented using degrees and percentages. Athlete gender and sport differences will be calculated using the ANOVA statistic. The p-value will be considered significant at the .05 level using a two-tailed test (α2 =.05).
Tipo de estudio
Inscripción (Anticipado)
Contactos y Ubicaciones
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Método de muestreo
Población de estudio
Descripción
Inclusion Criteria:
- Healthy student collegiate athletes
Exclusion Criteria:
- Presence of musculoskeletal, systemic or metabolic diseases that would affect lower extremity joint ROM or muscle function
- Presence of any current or past muscle or joint pathology of the hip, knee, and/or ankle that would affect lower extremity joint ROM or muscle function
- Inability to avoid exercise 4 hours prior to testing
- Inability to avoid medications that may affect the outcome of lower extremity joint ROM or muscle function
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
Cohortes e Intervenciones
Grupo / Cohorte |
|---|
|
Division II Collegiate Athletes
Student athletes (18-45) currently enrolled and participating on a sports team.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Periodo de tiempo |
|---|---|
|
Hip Joint Internal and External Rotation ROM
Periodo de tiempo: Baseline
|
Baseline
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Scott W Cheatham, DPT, PhD, California State University, Dominguez Hills
Publicaciones y enlaces útiles
Publicaciones Generales
- Shimamura KK, Cheatham S, Chung W, Farwell D, De la Cruz F, Goetz J, Lindblom K, Powers D. Regional interdependence of the hip and lumbo-pelvic region in divison ii collegiate level baseball pitchers: a preliminary study. Int J Sports Phys Ther. 2015 Feb;10(1):1-12.
- Prather H, Harris-Hayes M, Hunt DM, Steger-May K, Mathew V, Clohisy JC. Reliability and agreement of hip range of motion and provocative physical examination tests in asymptomatic volunteers. PM R. 2010 Oct;2(10):888-95. doi: 10.1016/j.pmrj.2010.05.005. Erratum In: PM R. 2011 Mar;3(3):286.
- Krause DA, Hollman JH, Krych AJ, Kalisvaart MM, Levy BA. Reliability of hip internal rotation range of motion measurement using a digital inclinometer. Knee Surg Sports Traumatol Arthrosc. 2015 Sep;23(9):2562-7. doi: 10.1007/s00167-014-3096-0. Epub 2014 Jun 11.
- Roach S, San Juan JG, Suprak DN, Lyda M. Concurrent validity of digital inclinometer and universal goniometer in assessing passive hip mobility in healthy subjects. Int J Sports Phys Ther. 2013 Oct;8(5):680-8.
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Finalización primaria (Anticipado)
Finalización del estudio (Anticipado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
Actualizaciones de registros de estudio
Última actualización publicada (Estimar)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Otros números de identificación del estudio
- 16-208
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
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. .