Accelerometers to investigate the quality of movement in patients with obstetric lesion of the brachial plexus (using the BPOM assessment)

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00029007

Enrollment

Registered

2024-11-20

Start date

2022-10-13

Completion date

Unknown

Last updated

2026-06-01

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

Conditions

P14.3

Interventions

Group 1: 50 subjects with obstetric brachial plexus lesion will be evaluated using inertial sensory testing and the Brachial Plexus Outcome Measure (BPOM). The examination will take a total of approx.

Eligibility

Sex/Gender

All

Age

13 Years to 60 Years

Inclusion criteria

Inclusion criteria: obstetric plexus lesion

Exclusion criteria

Exclusion criteria: - Cognitively unable to follow the movement instructions - No active range of motion of the upper extremity - Lack of parental consent or consent of the adult patient - Lack of consent of the child - Pregnancy - Existing neuromuscular complaints or a history of orthopedic surgery, and any type of upper extremity impairment in addition to the plexus lesion.

Design outcomes

Primary

Measure	Time frame
Demonstration that quantification of movement ability via an algorithm can be divided into classes that reflect classification in the BPOM.	—

Countries

Germany

Contacts

Public ContactTim Leypold

Universitätsklinikum der RWTH Aachen

plastische-chirurgie@ukaachen.de0241 80 89700

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Jun 11, 2026