ClinicalTrials.gg
RecruitingNCT06851988Updated Sep 24, 2026

Can Exercise Ameliorate Immunosenescence and Thereby Reduce Relapse in Head and Neck Cancer Patients

An interventional study of HIIT & Record of physical activities at home. and HIIT only in Aging, High-intensity Interval Training and Head and Neck Cancers - Tonsils, sponsored by Chang Gung Memorial Hospital. Recruiting at 1 site in Taiwan. Open to participants aged 20 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-09-24.

Primary conditionHead and Neck NeoplasmsRegistry: Motor ActivityReclassifiedWhy we changed it
Registry
Motor Activity — the first condition term the registry derived for this study.
ClinicalTrials.gg
Head and Neck Neoplasms
Why
  1. Motor Activity is a broad heading, used only when no more specific condition is named.
  2. The study's listed conditions name Head and Neck Neoplasms.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Chang Gung Memorial Hospital · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 9 months after the study started (first participant enrolled May 2023, registered Feb 2024).
  • Started May 2023; still recruiting 3 years 6 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
290
Allocation
Randomized
Ages
20 Years to 80 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 22 studies in Head and Neck Neoplasms by Chang Gung Memorial Hospital — 7 open to participants now, 7 under way, none of them phase 3. Head and Neck Neoplasms · Chang Gung Memorial Hospital.

Started
2023
with 1 other
No phase
7 of 22
5 open now
Registered
17th of 22
by date

Among the 22 studies in Head and Neck Neoplasms by Chang Gung Memorial Hospital, this one is one of 2 that started in 2023, is one of 7 with no phase, and was the 17th registered.

By phase

22 studies; the count open now beside each. This study's row is marked.

Observational13 · 1 open
No phasethis study7 · 5 open
Phase 22 · 1 open

By the year they started

First in 2008; this study’s year is marked. 2 started in 2023.

Size and results

Median enrollment 92 across the 9 interventional studies, 150 across the 13 observational. Of the 9 that completed or were terminated, 0 (0%) have results posted.

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Watch this landscapeDownload CSVWith an account: a weekly mail of what changed among 22 studies in Head and Neck Neoplasms by Chang Gung Memorial Hospital, or all of them as a file.
02

Study summary

Through the implementation of this three-year project, investigators expect to find a safe and effective exercise prescription for patients with oral cancer after surgery. The findings will encourage and promise and add further support to the concept that exercise prescription is worth implementation as part of care for the patients with head and neck cancer.

Read the detailed description

Cancer patients have theoretically returned to a disease-free state after receiving curative anticancer therapy, but even after receiving adjuvant concurrent chemoradiotherapy, it does not ideally prevent all cancer recurrences. For that, several guidelines recommend that cancer survivors participate in regular exercise. Exercise has been thought to be associated with improved outcomes and mortality in healthy individuals as well as in certain cancer populations. However, while the most robust evidence has been demonstrated in patients with prostate, breast and colorectal cancers, the effectiveness of exercise interventions in Head and Neck cancer survivors remains inadequately understood.

Aging of the immune system (so-called immunosenescence) has long been known to increase the risk of infection, cancer, chronic inflammatory diseases and age-related multi-morbidity in humans. In the literature, patients with oral cavity cancer are also believed to have the phenomenon of immune aging (immunosenescence). One of the mechanisms that maintain cellular homeostasis and prevent immunosenescence-related damage is autophagy, a cell-survival mechanism, and it has been proposed as one of the most powerful antiaging therapies. Regular exercise can reestablish autophagy, probably through AMP-activated protein kinase activation, and help in reducing the age-related senescence diseases. At present, many research teams in cancer centers are trying to design large-scale prospective trials to answer whether the intervention of exercise can avoid cancer occurrence, health promotion in survivors, and prevention of recurrence.

This project focuses on the integration of the basic and clinical research. The multidisciplinary research team consists of members from the Department of Hematology and Oncology and Department of Rehabilitation of the New Taipei City Tucheng Hospital and Linkou Chang Gung Memorial Hospital. The main purpose of this three-year project is to investigate whether high-intensity interval training (HIIT) along with resistance exercise intervention, which could reduce the recurrence rate by ameliorating immunosenescence on patients with head and neck cancer. The main tasks order by year of this project are as the following: (1) investigating the differences of immunosenescence indicators in blood with before and after conducting eight weeks of HIIT along with resistance exercise training for patients with head and neck cancer (1st year plan); (2) recruiting new subjects, gathering the physical activity at home and the cancer recurrence rate for first-year subjects, investigating the differences of immunosenescence indicators and immune indicators in the peripheral blood, and examining the clinical effectiveness of exercise training (2nd year plan); (3) Tracking the clinical data and research materials for subjects recruited during the first and second years (3rd year plan). Through the implementation of this three-year project, investigators expect to find a safe and effective exercise prescription for patients with oral cancer after surgery. The findings will provide promising evidence and add further support to the concept that exercise prescription is worth implementation as part of care for the patients with head and neck cancer.

03

Conditions studied

  • Aging
  • High-intensity Interval Training
  • Head and Neck Cancers - Tonsils

Browse trials for

Keywords

  • Exercise
  • Immunosenescence
  • Recurrence-free survival
  • Head and Neck Cancer
04

In context

Head and Neck Neoplasms Reclassified

2,710 studies on the registry are indexed under Head and Neck Neoplasms; 594 are open to participants now.

This study's planned enrollment of 290 is above the median of 46 across 2,032 interventional studies indexed under Head and Neck Neoplasms.

Browse Head and Neck Neoplasms studies →

Lead sponsor

Chang Gung Memorial Hospital is the lead sponsor of 1,096 studies on the registry; 239 are open to participants now.

Compared within Head and Neck Neoplasms, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Motor Activity. The counts are of registry records indexed under each term, refreshed daily. How we classify →

05

Who can participate

Ages eligible
20 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Age ≥20
  2. Pathology:Squamous cell carcinoma
  3. Need CCRT treatment
  4. PS\<2
  5. Agree with blood drawing, excise training, questionnaire

Exclusion criteria

Exclusion Criteria:

  1. PS≥2
  2. Unable to tolerate basic exercise, or CCRT treatment
  3. Mental illness or any medical illness or concurrent illness that may be aggravated by exercise training or unmanageable
  4. Any medical condition that unsuitable for exercise
  5. Disagree to trial procedures: exercise, blood draws, questionnaire
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

ECOG performance status

A scale of how much an illness limits everyday activity. For people being assessed to join a study, scores run from 0 (fully active) to 4; lower is more active.

0
Fully active, no restrictions.
1
Limited in strenuous activity, but walking and able to do light work, such as housework or office work.
2
Walking and able to look after yourself, but unable to work; up and about more than half of waking hours.
3
Able to look after yourself only in part; in bed or a chair more than half of waking hours.
4
Unable to look after yourself at all; in bed or a chair all day.

Studies most often ask for 0–1 or 0–2. Your doctor gives the score; the WHO scale uses the same steps. The full scale also has 5, which records death.

06

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
290 participants (estimated)

Study arms

  • Experimental
    Head and Neck patient after CCRT treatment with HIIT training-Experimental group

    After CCRT treatment 4-5 week arrange HIIT training for patient. Two to three times a week ,total 24-36 times. keep follow the PFS and OS

    Other: HIIT & Record of physical activities at home. · Other: HIIT only

  • No intervention
    Head and Neck patient after CCRT treatment-Experimental group

    keep follow the PFS and OS

  • Experimental
    Head and Neck patient after CCRT treatment with HIIT training-Validation group

    After CCRT treatment 4-5 week arrange HIIT training for patient. Two to three times a week ,total 24-36 times. keep follow the PFS and OS

    Other: HIIT & Record of physical activities at home. · Other: HIIT only

  • No intervention
    Head and Neck patient after CCRT treatment-Validation group

    keep follow the PFS and OS

Interventions

  • OtherHIIT & Record of physical activities at home.

    After CCRT treatment 4-5 week arrange HIIT excise for patient two to three times a week 24-36 times. And record of physical activities at home. According to the record set goal to acheive.

  • OtherHIIT only

    After CCRT treatment 4-5 week arrange HIIT excise for patient two to three times a week 24-36 times.

07

What researchers measure

Primary outcomes

  1. percent of participants with phenoage and age

    To evaluate the phenoage acceleration by calculating differencehe of patients with phenoage and age.

    Time frame: baseline before CCRT

  2. percent of participants with phenoage and age

    To evaluate the phenoage acceleration by calculating differencehe of patients with phenoage and age.

    Time frame: 1 months after the completion of CCRT

  3. percent of participants with phenoage and age

    To evaluate the phenoage acceleration by calculating differencehe of patients with phenoage and age.

    Time frame: 6 months after the completion of CCRT

  4. percent of participants with phenoage and age

    To evaluate the phenoage acceleration by calculating differencehe of patients with phenoage and age.

    Time frame: 9 months after the completion of CCRT

  5. Peak VO2 (ml/min/kg) of participants

    To record the Peak VO2 (ml/min/kg) of participants and to evulate the effectiveness of exercise training

    Time frame: baseline before CCRT

  6. Peak VO2 (ml/min/kg) of participants

    To record the Peak VO2 (ml/min/kg) of participants and to evulate the effectiveness of exercise training.The higher scores mean a better outcome.

    Time frame: 1 months after the completion of CCRT

  7. Peak VO2 (ml/min/kg) of participants

    To record the Peak VO2 (ml/min/kg) of participants and to evulate the effectiveness of exercise training.The higher scores mean a better outcome.

    Time frame: 6 months after the completion of CCRT

  8. Peak VO2 (ml/min/kg) of participants

    To record the Peak VO2 (ml/min/kg) of participants and to evulate the effectiveness of exercise training. The higher scores mean a better outcome.

    Time frame: 9 months after the completion of CCRT

  9. Questionnaire of European Organisation for Research and Treatment of Cancer Quality of Life Head and Neck Module (EORTC QLQ-HN43)

    To assese the quality of life at the Head and Neck participants and evulate the effectiveness of exercise training.The minimum value is 43 and the maximum value is 172. The higher scores mean a worse outcome.

    Time frame: baseline before CCRT

  10. Questionnaire of European Organisation for Research and Treatment of Cancer Quality of Life Head and Neck Module (EORTC QLQ-HN43)

    To assese the quality of life at the Head and Neck participants and evulate the effectiveness of exercise training.The minimum value is 43 and the maximum value is 172. The higher scores mean a worse outcome.

    Time frame: 1 month after the completion of CCRT

  11. Questionnaire of European Organisation for Research and Treatment of Cancer Quality of Life Head and Neck Module (EORTC QLQ-HN43)

    To assese the quality of life at the Head and Neck participants and evulate the effectiveness of exercise training.The minimum value is 43 and the maximum value is 172. The higher scores mean a worse outcome.

    Time frame: 6 month after the completion of CCRT

  12. Questionnaire of European Organisation for Research and Treatment of Cancer Quality of Life Head and Neck Module (EORTC QLQ-HN43)

    To assese the quality of life at the Head and Neck participants and evulate the effectiveness of exercise training.The minimum value is 43 and the maximum value is 172. The higher scores mean a worse outcome.

    Time frame: 9 month after the completion of CCRT

08

Study locations

1 of 1 sites recruiting
09

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

10

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started May 2023 (actual). Primary completion is estimated for Oct 2026, 41 months after the start.

Of 437 non-industry interventional studies with no phase under Head and Neck Neoplasms, half reached primary completion within 33 months of starting (the median), counting those still running; a quarter within 18 and three quarters within 71. This study's planned 41 months is above that.

Counting every sponsor, half of 455 studies reached it within 32 months; a quarter within 18 and three quarters within 70.

How these figures are worked out, and which studies are left out of them.

Registered
Feb 21, 2024
First posted
Feb 28, 2025
StartActual
May 3, 2023
Primary completionEst.
Oct 30, 2026
CompletionEst.
Oct 30, 2026
Last update
Sep 24, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 24, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT06851988
Responsible party
Jason Chia-Hsun Hsieh (Professor, Chang Gung Memorial Hospital) — Principal investigator
First posted
Feb 28, 2025
Start date
May 3, 2023
Primary completion
Oct 30, 2026 (estimated)
Completion
Oct 30, 2026 (estimated)
Last update
Sep 24, 2026

Study contacts

Wan-Chin Kuo
Contact
troublefup6@cgmh.org.tw
03-3196200 ext. 3708
Kuo
Contact
Chia-Hsun Hsieh
study chair · New Tipei City Tucheng Hospital

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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