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Study identifier: NCT07689019 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Effects of Far Infrared Rays and Transcutaneous Electrical Nerve Stimulation on Short Term Prognosis of Head and Neck Cancer Patients Receiving Curative Treatment

Condition: Head and Neck Cancer (H&N)  ·  Sponsor: Buddhist Tzu Chi General Hospital

PhaseNA
Planned participants102
Who can joinAll sexes, 30 Years to 85 Years
Healthy volunteersNo

About this study

This clinical trial aims to evaluate whether far infrared radiation therapy and transcutaneous electrical nerve stimulation can reduce treatment-related side effects in patients with head and neck cancer undergoing concurrent chemoradiotherapy. The primary objectives of this study are to determine whether far infrared radiation therapy and transcutaneous electrical nerve stimulation can improve shoulder pain and disability, cervical range of motion, maximum interincisal distance, oral mucositis, systemic inflammation, and chemotherapy-induced nausea and vomiting. Participants will be randomly assigned to one of three groups: Group A will receive standard care (control group); Group B will receive standard care plus transcutaneous electrical nerve stimulation; and Group C will receive standard care plus far infrared radiation therapy combined with transcutaneous electrical nerve stimulation. The intervention will be administered over two cycles of concurrent chemoradiotherapy, for a total of 10 intervention days. During each treatment cycle, participants in the intervention groups will receive the assigned treatment once every morning and once every evening for five consecutive days. Outcome assessments will be performed at three time points during each treatment cycle: before the intervention on Day 1 (baseline), after the intervention on Day 3, and after the intervention on Day 5.

This description comes directly from the study's public registry record.

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Locations (1)

Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical FoundationHualien City, Hualien County, TaiwanRecruiting

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Source record: clinicaltrials.gov/study/NCT07689019