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Anchoring and Postural Stability

17 de septiembre de 2026 actualizado por: William J. Hanney, University of Central Florida

Anchoring and Its Effects on Postural Stability

This study will compare standing balance in adults ages 18 to 50 during normal standing, inward anchoring, and outward anchoring. Anchoring involves standing with the feet wider than shoulder width and trying to pull the legs together or push them apart without moving the feet. Participants will complete all three conditions in a randomly assigned order. A researcher will use a handheld force-measuring instrument at six points on the pelvis to measure how much pressure participants can resist before a foot lifts from the floor. Participants will also rate how stable they feel after each anchoring condition. The first 18 participants will repeat assessments to evaluate measurement consistency. Participation is expected to last 60 minutes, or 90 minutes for those completing repeat assessments.

Descripción general del estudio

Descripción detallada

The study will enroll 72 adults from the University of Central Florida community. Participants will be randomized with equal probability to one of six counterbalanced orders of normal stance, inward anchoring, and outward anchoring. Every participant will complete all three conditions.

Inward anchoring involves attempting to draw the legs toward one another without moving the feet. Outward anchoring involves attempting to press the legs away from one another without moving the feet. Both anchoring conditions use a stance wider than shoulder width. Participants will wear their usual athletic footwear.

The same tester will apply a microFET2 handheld dynamometer at the right and left anterior superior iliac spines, iliac crests, and posterior superior iliac spines. Applied pressure will increase until the sole of the foot closest to the tester leaves the floor, at which point force will be recorded in newtons. Each site will be tested three times in each stance. Rest periods will be one minute between sets within a stance and two minutes between stances. Instructions for the next stance will be given during the final minute of the between-stance rest period.

After each anchoring condition, participants will rate perceived stability. The first 18 participants will complete additional repeat assessments for intrarater reliability analysis. The protocol plans repeated-measures analyses for stance/order comparisons and intraclass correlation coefficients for reliability.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

72

Fase

  • No aplica

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.

Estudio Contacto

Ubicaciones de estudio

    • Florida
      • Orlando, Florida, Estados Unidos, 32816
        • Reclutamiento
        • University of Central Florida Spine and Mobility Lab
        • Contacto:

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

18 años a 50 años (Adulto)

Acepta Voluntarios Saludables

Sí

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • Adults aged 18-50 years.
  • Able to provide informed consent and independently read, write, and communicate in English.

Exclusion Criteria:

  • History of neurological or vestibular conditions affecting balance, such as stroke, Parkinson's disease, multiple sclerosis, or vertigo, or uncorrected/inadequately corrected visual deficits affecting postural control.
  • Lower-extremity or spinal injury, orthopedic surgery, or a musculoskeletal condition within the past 6-12 months that may affect balance, force production, or safe participation.
  • Current pain or dysfunction limiting safe standing or weight-bearing tasks.
  • Use of medications that may affect balance, coordination, or muscle performance, such as muscle relaxants, opioids, or sedatives.
  • A cardiovascular or systemic condition that makes participation unsafe, such as uncontrolled hypertension, dizziness, or syncope, or inability to stand independently for the duration of testing.

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

  • Propósito principal: Poner en pantalla
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación cruzada
  • Enmascaramiento: Doble

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Normal Stance → Inward Anchoring → Outward Anchoring

Participants complete normal stance, then inward anchoring, then outward anchoring. The same force assessments are performed in each condition, with two minutes of rest between conditions.

Participants stand normally while the tester performs the protocol's pelvic force assessments. This condition provides the within-participant comparison for the two anchoring techniques

Participants stand upright with their feet wider than shoulder width and attempt to pull their legs toward each other without moving the feet. They maintain the position during the pelvic force assessments.

Participants stand upright with their feet wider than shoulder width and attempt to push their legs away from each other without moving the feet. They maintain the position during the pelvic force assessments.

Experimental: Normal Stance → Outward Anchoring → Inward Anchoring

Participants complete normal stance, then outward anchoring, then inward anchoring. The same force assessments are performed in each condition, with two minutes of rest between conditions.

Participants stand normally while the tester performs the protocol's pelvic force assessments. This condition provides the within-participant comparison for the two anchoring techniques

Participants stand upright with their feet wider than shoulder width and attempt to pull their legs toward each other without moving the feet. They maintain the position during the pelvic force assessments.

Participants stand upright with their feet wider than shoulder width and attempt to push their legs away from each other without moving the feet. They maintain the position during the pelvic force assessments.

Experimental: Outward Anchoring → Normal Stance → Inward Anchoring

Participants complete outward anchoring, then normal stance, then inward anchoring. The same force assessments are performed in each condition, with two minutes of rest between conditions.

Participants stand normally while the tester performs the protocol's pelvic force assessments. This condition provides the within-participant comparison for the two anchoring techniques

Participants stand upright with their feet wider than shoulder width and attempt to pull their legs toward each other without moving the feet. They maintain the position during the pelvic force assessments.

Participants stand upright with their feet wider than shoulder width and attempt to push their legs away from each other without moving the feet. They maintain the position during the pelvic force assessments.

Experimental: Outward Anchoring → Inward Anchoring → Normal Stance

Participants complete outward anchoring, then inward anchoring, then normal stance. The same force assessments are performed in each condition, with two minutes of rest between conditions.

Participants stand normally while the tester performs the protocol's pelvic force assessments. This condition provides the within-participant comparison for the two anchoring techniques

Participants stand upright with their feet wider than shoulder width and attempt to pull their legs toward each other without moving the feet. They maintain the position during the pelvic force assessments.

Participants stand upright with their feet wider than shoulder width and attempt to push their legs away from each other without moving the feet. They maintain the position during the pelvic force assessments.

Experimental: Inward Anchoring → Normal Stance → Outward Anchoring

Participants complete inward anchoring, then normal stance, then outward anchoring. The same force assessments are performed in each condition, with two minutes of rest between conditions.

Participants stand normally while the tester performs the protocol's pelvic force assessments. This condition provides the within-participant comparison for the two anchoring techniques

Participants stand upright with their feet wider than shoulder width and attempt to pull their legs toward each other without moving the feet. They maintain the position during the pelvic force assessments.

Participants stand upright with their feet wider than shoulder width and attempt to push their legs away from each other without moving the feet. They maintain the position during the pelvic force assessments.

Experimental: Inward Anchoring → Outward Anchoring → Normal Stance

Participants complete inward anchoring, then outward anchoring, then normal stance. The same force assessments are performed in each condition, with two minutes of rest between conditions.

Participants stand normally while the tester performs the protocol's pelvic force assessments. This condition provides the within-participant comparison for the two anchoring techniques

Participants stand upright with their feet wider than shoulder width and attempt to pull their legs toward each other without moving the feet. They maintain the position during the pelvic force assessments.

Participants stand upright with their feet wider than shoulder width and attempt to push their legs away from each other without moving the feet. They maintain the position during the pelvic force assessments.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Mean Break-Point Force at the Right Anterior Superior Iliac Spine
Periodo de tiempo: Day 1

A microFET2 handheld dynamometer is applied at the right anterior superior iliac spine during normal stance, inward anchoring, and outward anchoring. Force in newtons is recorded when the sole of the foot closest to the tester leaves the floor. Three readings are collected per stance

Day 1
Mean Break-Point Force at the Left Anterior Superior Iliac Spine
Periodo de tiempo: Day 1

A microFET2 handheld dynamometer is applied at the left anterior superior iliac spine during normal stance, inward anchoring, and outward anchoring. Force in newtons is recorded when the sole of the foot closest to the tester leaves the floor. Three readings are collected per stance.

Day 1
Mean Break-Point Force at the Right Iliac Crest
Periodo de tiempo: Day 1

A microFET2 handheld dynamometer is applied at the right iliac crest during normal stance, inward anchoring, and outward anchoring. Force in newtons is recorded when the sole of the foot closest to the tester leaves the floor. Three readings are collected per stance

Day 1
Mean Break-Point Force at the Left Iliac Crest
Periodo de tiempo: Day 1

A microFET2 handheld dynamometer is applied at the left iliac crest during normal stance, inward anchoring, and outward anchoring. Force in newtons is recorded when the sole of the foot closest to the tester leaves the floor. Three readings are collected per stance.

Day 1
Mean Break-Point Force at the Right Posterior Superior Iliac Spine
Periodo de tiempo: Day 1

A microFET2 handheld dynamometer is applied at the right posterior superior iliac spine during normal stance, inward anchoring, and outward anchoring. Force in newtons is recorded when the sole of the foot closest to the tester leaves the floor. Three readings are collected per stance.

Day 1
Mean Break-Point Force at the Left Posterior Superior Iliac Spine
Periodo de tiempo: Day 1

A microFET2 handheld dynamometer is applied at the left posterior superior iliac spine during normal stance, inward anchoring, and outward anchoring. Force in newtons is recorded when the sole of the foot closest to the tester leaves the floor. Three readings are collected per stance.

Day 1
Perceived Stability Rating After Inward Anchoring
Periodo de tiempo: Day 1

After inward anchoring, participants answer how stable they felt during that stance. Ratings range from 0 (not at all stable) to 10 (completely stable); 5 means neutral, or the same stability as normal standing. Higher scores indicate greater perceived stability.

Day 1
Perceived Stability Rating After Outward Anchoring
Periodo de tiempo: Day 1

After outward anchoring, participants answer how stable they felt during that stance. Ratings range from 0 (not at all stable) to 10 (completely stable); 5 means neutral, or the same stability as normal standing. Higher scores indicate greater perceived stability

Day 1

Colaboradores e Investigadores

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

Investigadores

  • Investigador principal: William J Hanney, PhD, University of Central Florida

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Publicaciones Generales

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 (Actual)

23 de agosto de 2026

Finalización primaria (Estimado)

30 de septiembre de 2027

Finalización del estudio (Estimado)

2 de mayo de 2028

Fechas de registro del estudio

Enviado por primera vez

9 de septiembre de 2026

Primero enviado que cumplió con los criterios de control de calidad

17 de septiembre de 2026

Publicado por primera vez (Actual)

24 de septiembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

24 de septiembre de 2026

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

17 de septiembre de 2026

Última verificación

1 de septiembre de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • 9152

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

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. .

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