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AI-based Physiotherapy for Oral Cancer Patients

Effects of AI-Based Physiotherapy on Mandibular Mobility, Shoulder Function, Whole-Body Physical Function, and Quality of Life in Oral Cancer Patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06785051
Enrollment
100
Registered
2025-01-20
Start date
2025-02-19
Completion date
2027-07-31
Last updated
2026-04-03

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

Conditions

Oral Cancer

Keywords

Artificial intelligence, Oral cancer, Maximum interincisal opening, Physical function, Prehabilitation, Physiotherapy

Brief summary

This study examines the effects of AI-based physiotherapy on oral function, shoulder function, whole-body physical function, and quality of life in oral cancer patients. One hundred patients will be recruited before surgery, chemotherapy, or radiotherapy and randomly assigned to an experimental group receiving 12 weeks of AI-guided physiotherapy or a control group receiving usual care. Both groups will perform jaw, neck, and shoulder exercises, with the experimental group using a mobile app to monitor progress. Assessments at baseline, pre-intervention, and 3 months post-intervention will measure maximal in the maximum interincisal opening (MIO), joint range of motion (ROM), pain, endurance (e.g., 6-minute walk test), upper extremity function, and quality of life.

Detailed description

This study examines the effects of AI-based physiotherapy on oral function (e.g., mouth opening), shoulder function (e.g., shoulder joint range of motion and upper extremity function), whole-body physical function (e.g., 6-minute walk test), and health-related quality of life. 100 newly diagnosed oral cancer patients will be recruited before surgery, chemotherapy, or radiotherapy and randomly assigned to two groups. The experimental group will receive AI-based physiotherapy for 12 weeks, including postural correction exercises guided by AI technology, while the control group will receive usual care. Both groups will perform jaw, neck, and shoulder exercises, with the experimental group using a mobile app to monitor progress and record their exercise diaries. Assessments at baseline, pre-intervention, and 3 months post-intervention will measure the maximum interincisal opening (MIO), joint range of motion (ROM), pain, endurance, and upper extremity function using the Disabilities of the Arm, Shoulder, and Hand (DASH) scores, and quality of life using the European Organization for Research and Treatment of Cancer Core Quality of Life Questionnaire (EORTC QLQ-C30).

Interventions

jaw, neck, shoulder ROM exercises, and scapular-focused exercises guided by AI technology, 30 minutes of intervention, once a week, and a total of 12 weeks

BEHAVIORALConventional physiotherapy

jaw, neck, shoulder ROM exercises, and scapular-focused exercises, 30 minutes of intervention, once a week, and a total of 12 weeks

BEHAVIORALScar management

scar massage and jaw-mobilizing exercises combined with devices or depressors

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Newly diagnosed oral cancer patients who are scheduled to receive cancer-related treatments (e.g., oral cancer surgery, radiotherapy, chemotherapy, or chemoradiotherapy). * Age between 20 and 65 years.

Exclusion criteria

* Could not communicate. * Had any disorder that could influence movement performance.

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in maximal mouth openingbaseline, pre-intervention, 3-months post-interventionAverage maximal mouth opening measured 3 times in mm
Change from baseline in shoulder joint range of motionbaseline, pre-intervention, 3-months post-interventionAverage range of motion of shoulder abduction measured 3 times in degrees

Secondary

MeasureTime frameDescription
Change from baseline in function on Disabilities of the Arm, Shoulder, and Hand outcome questionnairebaseline, pre-intervention, 3-months post-interventionA total scale from 1 to 100. Higher scores indicate greater disability.
Change from baseline in health-related function on EORTC QLQ-C30 questionnairebaseline, pre-intervention, 3-months post-interventionA total scale from 1 to 100. Higher scores indicate greater function.
Change from baseline in whole-body physical function on 6-minute walk testbaseline, pre-intervention, 3-months post-interventionWalking distance measured in meters.
Change from baseline in shoulder painbaseline, pre-intervention, 3-months post-interventionVisual analog scale from 0 to 10. Higher scores indicate most pain.

Countries

Taiwan

Contacts

CONTACTYueh-Hsia Chen, PhD
yuehhsiachen@ntu.edu.tw+886-2-33668133
PRINCIPAL_INVESTIGATORYueh-Hsia Chen, PhD

National Taiwan University, College of Medicine

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 4, 2026