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RecruitingNCT07754162Updated Aug 10, 2026

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

An observational study in Reliability and Ultrasound, sponsored by Riphah International University. Recruiting at 1 site in Pakistan. Open to male participants aged 18 Years to 40 Years. Per ClinicalTrials.gov, last updated 2026-08-10.

Sponsored by Riphah International University · Observational

Study type
Observational
Model
Other
Time perspective
Retrospective
Enrollment
50
Ages
18 Years to 40 Years
Sex
Male
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Reliability
  • Ultrasound
03

Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
Male
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Non Athletes

Inclusion criteria

  • Recreationally Active

Exclusion criteria

Exclusion Criteria:

  • Known Musculoskeletal injury
04

Study design

Observational model
Other
Time perspective
Retrospective
Enrollment
50 participants (estimated)
Patient registry
No

Groups and cohorts

  • 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.

05

What researchers measure

Primary outcomes

  1. Inter-rater reliability of ultrasound-based rectus abdominis muscle thickness measurement

    Inter-rater reliability between two independent raters in measuring rectus abdominis muscle thickness from B-mode ultrasound images using ImageJ software.

    Time frame: Baseline (pre-training) and post-training ultrasound images obtained at the completion of the two-week BFR training protocol.

Secondary outcomes

  1. Inter-rater reliability of ultrasound-based rectus abdominis muscle thickness measurement

    Rectus abdominis muscle thickness

    Time frame: Pre-training and immediately post-training.

06

Study locations

1 of 1 sites recruiting
  • Faculty of Rehabilitation for Data Collection and Research Work
    Islamabad, 44000, Pakistan
    • Muhammad Haris · Contact · 03437181808
    Recruiting
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07754162
Lead sponsor
Riphah International University
Responsible party
Sponsor
First posted
Aug 10, 2026
Start date
Aug 4, 2026
Primary completion
Sep 6, 2026 (estimated)
Completion
Sep 20, 2026 (estimated)
Last update
Aug 10, 2026

Study contacts

Muhammad Haris, DPT
Contact
harismughal5154@gmail.com
03437181808
Dr Saad Rauf, PhD
Contact
03325957732
Saad Rauf, PhD
principal investigator · Riphah International University, Isra University, Islamabad

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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