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AI Based Physiotherapy 3- and 9-Month Follow-Up in Oral Cancer Patients

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National Taiwan University

Status

Enrolling

Conditions

Oral Cancer

Treatments

Other: AI-based physiotherapy follow-up assessments
Other: conventional physiotherapy follow-up assessments

Study type

Interventional

Funder types

Other

Identifiers

NCT07237672
202412109RIND

Details and patient eligibility

About

This follow-up clinical study aims to evaluate the sustained effects of two rehabilitation programs (AI-based physiotherapy vs. conventional physiotherapy) for oral cancer patients. Participants who completed the original intervention trial (ClinicalTrials.gov ID: 202411044RINC) will be assessed at 3 and 9 months post-intervention. Outcomes include mandibular mobility, shoulder joint range of motion, functional performance, quality of life, pain, and return-to-work status.

Full description

This study is a continuation of our prior trial (ClinicalTrials.gov ID: 202411044RINC), which investigated the short-term effects of AI-based physiotherapy compared with conventional physiotherapy in oral cancer patients.

The current follow-up phase evaluates both groups at 3 and 9 months post-intervention to determine whether initial improvements are maintained and whether they translate into better long-term physical function, quality of life, and return-to-work outcomes. No additional interventions will be delivered; only follow-up assessments are planned.

Enrollment

65 estimated patients

Sex

All

Ages

20 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Participants who completed the intervention phase of the previous trial (202411044RINC)
  • Age 20-65 years
  • Able to attend follow-up assessments at 3 and 9 months

Exclusion criteria

  • Withdrawal from the original trial
  • Cancer recurrence or new cancer-related treatment interfering with functional assessment
  • Unable to communicate or comply with follow-up visits

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

65 participants in 2 patient groups

Experimental group (Follow-up)
Experimental group
Description:
Participants who originally received AI-based physiotherapy will undergo follow-up assessments at 3 and 9 months post-intervention.
Treatment:
Other: AI-based physiotherapy follow-up assessments
Control group (Follow-up)
Active Comparator group
Description:
Participants who originally received conventional physiotherapy will undergo follow-up assessments at 3 and 9 months post-intervention.
Treatment:
Other: conventional physiotherapy follow-up assessments

Trial contacts and locations

1

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Central trial contact

Yueh-Hsia Chen, Ph.D.

Data sourced from clinicaltrials.gov

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