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Estimating Jaw, Neck, and Shoulder Range of Motion Using an AI Model

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National Taiwan University

Status

Enrolling

Conditions

Oral Cancer

Treatments

Behavioral: observation alone

Study type

Observational

Funder types

Other

Identifiers

NCT06629038
202403103RINA

Details and patient eligibility

About

This observational study aims to develop an AI-based system for tracking mandibular and shoulder movements using deep learning techniques. It will compare AI-generated pose estimations with gold standard measurements to assess accuracy, particularly in patients with functional impairments from oral cancer treatment, such as trismus, spinal accessory nerve dysfunction, neck dystonia, and radiation fibrosis.

Full description

Due to the involvement of various structures, patients with oral cancer may experience functional impairments after treatment, such as trismus, spinal accessory nerve dysfunction, neck dystonia, radiation fibrosis, and fatigue. This observational study aims to develop an AI-based system for tracking mandibular and shoulder movements using deep learning techniques. AI-generated pose estimations will be compared with gold standard measurements: maximal mouth opening will be compared with caliper measurements, and Therabilte scale, while shoulder abduction range of motion will be compared with universal goniometer measurements. We will recruit 20 healthy adults and 20 oral cancer patients. Data on maximal mouth opening and shoulder abduction will be collected through video recordings, calipers, Therabilte scale, and universal goniometers. The videos will be analyzed using deep learning to estimate mouth opening and shoulder abduction angles. These estimates will then be compared with the gold standard measurements. The Intraclass Correlation Coefficient (ICC), Mean Absolute Error (MAE), and Coefficient of Variation (CV) will be used as performance indicators to assess and compare the reliability, accuracy, and consistency of the models.

Enrollment

40 estimated patients

Sex

All

Ages

20 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy adults without a history of head, neck or shoulder injury or surgery, and without HNC-related radiotherapy or chemoradiotherapy
  • Oral cancer patients with trismus, clinical signs of neck or shoulder joint impairment after oral cancer surgery or radiotherapy
  • Age between 20 and 65 years

Exclusion criteria

  • Could not communicate
  • Had any disorder that could influence movement performance

Trial design

40 participants in 2 patient groups

oral cancer patients
Description:
oral cancer patients with trismus, neck, or shoulder problems
Treatment:
Behavioral: observation alone
healthy adults
Description:
healthy adults without history of trismus, neck, or shoulder problems
Treatment:
Behavioral: observation alone

Trial contacts and locations

1

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Central trial contact

Yueh-Hsia Chen, PhD

Data sourced from clinicaltrials.gov

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