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Palpatory and Ultrasonographic Assessment of Tissue Compressibility: Validation and Learning Effects in Phantom Models

Palpatory and Ultrasonographic Assessment of Tissue Compressibility: Validation and Learning Effects in Phantom Models

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07386782
Enrollment
40
Registered
2026-02-04
Start date
2026-01-31
Completion date
2026-05-31
Last updated
2026-04-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diagnostic Ultrasound, Exanimation, Palpation

Keywords

Exanimation, Diagnostic Ultrasound, Palpation

Brief summary

This validation study compares clinical palpation and ultrasonographic measurements of tissue compressibility using standardized phantom models. Operators with different levels of clinical and ultrasound experience perform repeated, blinded assessments across multiple sessions. The study evaluates accuracy, reliability, agreement between modalities, and learning effects over time, aiming to support standardized and more objective assessment of tissue compressibility in clinical practice.

Interventions

BEHAVIORALUltrasonographic Compression Measurment and Palpation of Standardized Phantom Models

Repeated ultrasonographic compression measurements and palpation of standardized phantom models

Sponsors

Insel Gruppe AG, University Hospital Bern
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Medical professionals and medical students

Exclusion criteria

* Age \<18 years

Design outcomes

Primary

MeasureTime frameDescription
Accuracy and reliability of palpation and ultrasonographic compression measurementsOver 3 sessions, seperated by at least 1 day and at most 1 week (study duration: 3 days to 2 weeks)Intraoperator and interoperator accuracy and reliability of palpation and ultrasonographic compression measurements on two phantom models as intraclass correlation coefficient and linear mixed-effects model

Secondary

MeasureTime frameDescription
Effect of operator characteristics on the measurement accuracy and reliability.Over 3 sessions, seperated by at least 1 day and at most 1 week (study duration: 3 days to 2 weeks)Operator characteristics (age, gender, level of experience) will be introduced as fixed effects in a linear mixed-effects model with a random effect for participants to account for repeated measurements
Assess the learning curve in palpation and ultrasound measurementsOver 3 sessions, seperated by at least 1 day and at most 1 week (study duration: 3 days to 2 weeks)Changes in accuracy of both modalities using linear mixed-effects model with a random effect for participants to account for repeated measurements. To test possible confounding factors, they will be introduced as fixed effects.
Correlate the compression measurements with palpatory assessmentOver 3 sessions, seperated by at least 1 day and at most 1 week (study duration: 3 days to 2 weeks)Correlation of both modalities using linear mixed-effects model with a random effect for participants to account for repeated measurements. To test possible confounding factors, they will be introduced as fixed effects.

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 18, 2026