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Ultrasound tissue characterisation for the biceps femoris long head proximal tendon: A feasibility study

Ultrasound tissue characterisation for the biceps femoris long head proximal tendon: A feasibility study - Tendinopathy & hamstring UTC echo types: A feasibility study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON55782
Enrollment
26
Registered
2018-12-05
Start date
2022-04-10
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Sportblessures Hamstring strain injuries

Interventions

None listed

Sponsors

Universiteit Maastricht
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: To be eligible to participate in this study as a participant without PHT, the participant must meet all of the following criteria: - Between 18-65 years old; - Participating in sports that involve running, cycling or strength training for at least three two times per week. To be eligible to participate in this study as a participant with PHT, the participant must meet all of the following criteria: - Between 18-65 years old; - Background in, or currently active in a sport that involves running, cycling or strength training for at least two times per week; - Clinically diagnosed PHT.

Exclusion criteria

Exclusion criteria: A potential participant who meets any of the following criteria will be excluded from participation:- Severe visual or hearing impairment since this makes explanation of the correct position for imaging more difficult; - BMI outside 18-25, since excessive adipose tissue around the hip region will make it difficult to get clear images of the hamstrings tendon tissue; - Known cardiovascular or other diseases; - In accordance with a previous study13, hypoechoic areas on the tomographic planes in the 3-D volume of the UTC measurements did not lead to exclusion.For control participants, the following additional exclusion criteria apply:- History of a previous injury to the upper leg within the previous 5 years; - Pain, ache or soreness in the upper leg within the previous year n pijn en

Design outcomes

Primary

MeasureTime frame
Ultrasound tissue characterisation echo types

Secondary

MeasureTime frame
standard error of measurement and intraclass correlation coefficient and dynamic coherence (measure of the change in three-dimensional pennation angle).

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)