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Inter-Rater Reliability of Ultra Sound Based Rectus Abdominis Thickness Following Blood Flow Restriction Training

5 de agosto de 2026 actualizado por: Riphah International University

Inter-Rater Reliability of Ultra Sound Based Rectus Abdominis Thickness Following Blood Flow Restriction Training : A Retrospective Analysis.

Accurate assessment of skeletal muscle morphology is important in sports physiotherapy, exercise rehabilitation, and research. B-mode ultrasonography is a non-invasive and accessible method for assessing muscle thickness; however, ultrasound-based measurements may be influenced by image acquisition, anatomical landmark identification, and operator-dependent measurement procedures. Establishing inter-rater reliability is therefore essential to determine whether different assessors can obtain consistent measurements of muscle thickness from the same ultrasound images. The rectus abdominis is an important component of the abdominal musculature and contributes to trunk stabilization and functional performance during exercise. Blood flow restriction (BFR) training has gained increasing attention as a low-load exercise strategy for promoting muscular adaptations, although research has predominantly focused on peripheral limb muscles. Therefore, this study aims to evaluate the inter-rater reliability of ultrasound-based rectus abdominis muscle thickness measurements following a standardized BFR training protocol using ImageJ software. Establishing reliable measurement of rectus abdominis thickness will provide a methodological basis for future research investigating abdominal muscle morphology and adaptations in sports physiotherapy, exercise rehabilitation, and BFR-based training.

Descripción general del estudio

Estado

Reclutamiento

Condiciones

Descripción detallada

A retrospective methodological reliability study design will be employed to evaluate the inter-rater reliability of ultrasound-based measurements of rectus abdominis muscle thickness following a standardized blood flow restriction (BFR) training protocol. The study will utilize previously collected B-mode ultrasound images obtained from healthy young adult male participants who completed the original BFR training protocol. The existing dataset will be reviewed according to predefined eligibility criteria, and only ultrasound images of sufficient quality for identification and measurement of the rectus abdominis muscle will be included in the analysis.

The original BFR training protocol involved low-load resistance exercise performed under blood flow restriction. During the intervention, pneumatic cuffs were applied to the limbs, and participants performed a standardized squat exercise protocol at a low percentage of one-repetition maximum with prescribed repetitions and rest intervals. Ultrasound images of the rectus abdominis obtained according to the standardized imaging protocol will be analyzed retrospectively. The rectus abdominis was selected because it is a superficial abdominal muscle that can be visualized using B-mode ultrasonography and has relatively well-defined anatomical boundaries, allowing its thickness to be assessed using a standardized measurement procedure. Furthermore, the rectus abdominis contributes to trunk stabilization during functional and resistance exercises.

Ultrasound images will be analyzed using ImageJ software. Two independent raters will perform the measurements of rectus abdominis muscle thickness using the same standardized measurement protocol. The raters will independently identify the anatomical boundaries of the rectus abdominis and obtain linear thickness measurements from the ultrasound images. The use of a single standardized image-analysis platform and identical measurement procedures for both raters will minimize variability related to software and measurement techniques. The primary outcome will be the rectus abdominis muscle thickness measured in millimeters (mm).

Inter-rater reliability will be assessed using the Intraclass Correlation Coefficient (ICC) with a two-way random-effects model for absolute agreement and single measurements [ICC (2,1)], reported with the corresponding 95% confidence interval. ICC values below 0.50 will be interpreted as poor reliability, values from 0.50 to 0.75 as moderate reliability, values from 0.75 to 0.90 as good reliability, and values above 0.90 as excellent reliability. Absolute reliability and measurement error will additionally be assessed using the Standard Error of Measurement (SEM) and Minimal Detectable Change at the 95% confidence level (MDC95), where appropriate. Bland-Altman analysis will be performed to evaluate systematic differences and limits of agreement between the two raters. All statistical analyses will be conducted using SPSS, with the level of statistical significance set at p < 0.05.

If the ultrasound-based rectus abdominis thickness measurement demonstrates good to excellent inter-rater reliability, the findings will support the reproducibility of the standardized measurement protocol and its application in future research involving abdominal muscle morphology. The study may provide a methodological foundation for future investigations examining changes in abdominal muscle morphology following BFR and other exercise interventions, with potential relevance to sports physiotherapy, rehabilitation, and exercise science.

Tipo de estudio

De observación

Inscripción (Estimado)

50

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

Copia de seguridad de contactos de estudio

  • Nombre: Dr Saad Rauf, PhD
  • Número de teléfono: 03325957732

Ubicaciones de estudio

      • Islamabad, Pakistán, 44000
        • Reclutamiento
        • Faculty of Rehabilitation for Data Collection and Research Work
        • Contacto:
          • Muhammad Haris
          • Número de teléfono: 03437181808

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

  • Adulto

Acepta Voluntarios Saludables

No

Método de muestreo

Muestra no probabilística

Población de estudio

Non Athletes

Descripción

Inclusion Criteria:

  • Recreationally Active

Exclusion Criteria:

  • Known Musculoskeletal injury

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
Retrospective BFR Cohort
Healthy active male participants who underwent a short-duration blood flow restriction (BFR) training protocol. Pre- and post-training ultrasound images of the rectus abdominis muscle were retrospectively analyzed to assess inter-rater reliability of ultrasound-based muscle thickness measurements.
Group 1
Healthy active male participants assessed before the BFR training program. Baseline B-mode ultrasound images of the rectus abdominis muscle were obtained and used for measurement of muscle thickness.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Inter-rater reliability of ultrasound-based rectus abdominis muscle thickness measurement
Periodo de tiempo: Baseline (pre-training) and post-training ultrasound images obtained at the completion of the two-week BFR training protocol.
Inter-rater reliability between two independent raters in measuring rectus abdominis muscle thickness from B-mode ultrasound images using ImageJ software.
Baseline (pre-training) and post-training ultrasound images obtained at the completion of the two-week BFR training protocol.

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Inter-rater reliability of ultrasound-based rectus abdominis muscle thickness measurement
Periodo de tiempo: Pre-training and immediately post-training.
Rectus abdominis muscle thickness
Pre-training and immediately post-training.

Colaboradores e Investigadores

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

Investigadores

  • Investigador principal: Saad Rauf, PhD, Riphah International University, Isra University, Islamabad

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)

4 de agosto de 2026

Finalización primaria (Estimado)

6 de septiembre de 2026

Finalización del estudio (Estimado)

20 de septiembre de 2026

Fechas de registro del estudio

Enviado por primera vez

5 de agosto de 2026

Primero enviado que cumplió con los criterios de control de calidad

5 de agosto de 2026

Publicado por primera vez (Actual)

10 de agosto de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

10 de agosto de 2026

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

5 de agosto de 2026

Última verificación

1 de agosto de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • REC/MS-PT/02569

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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