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Not yet recruitingNCT06949618Updated May 18, 2025

Repetitive Transcranial Magnetic Stimulation in Cancer Pain Management

An interventional study of Repetitive transcranial magnetic stimulation (rTMS) in Pain and Cancer, sponsored by Taipei Medical University Hospital. Not yet recruiting at 1 site in Taiwan. Open to participants aged 20 Years to 70 Years. Per ClinicalTrials.gov, last updated 2025-05-18.

Sponsored by Taipei Medical University Hospital · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
20 Years to 70 Years
Sex
All
01

Study summary

Over half of cancer patients experience cancer-related pain. Despite advances in pain management with opioids, many patients continue to suffer from chronic cancer pain. The underlying mechanisms of cancer-related pain remain poorly understood, but they may be linked to brain neuroplasticity. As a result, some researchers suggest that targeting the motor cortex in cancer patients could improve pain management. However, few studies have investigated the effectiveness of remodeling neuroplasticity with repetitive transcranial magnetic stimulation (rTMS) to reduce cancer-related pain. To validate the use of rTMS in cancer-related pain, we plan to conduct a randomized controlled trial involving 30 cancer pain patients. Participants will be randomly assigned to receive either rTMS or sham rTMS treatment. Functional magnetic resonance imaging (fMRI) and pain index assessments will be conducted before and after the treatment to evaluate the outcomes.

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Conditions studied

  • Pain
  • Cancer
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In context

Pain

10,054 studies on the registry are indexed under Pain; 1,649 are open to participants now.

This study's planned enrollment of 30 is below the median of 66 across 8,493 interventional studies indexed under Pain.

Browse Pain studies →

Lead sponsor

Taipei Medical University Hospital is the lead sponsor of 64 studies on the registry; 12 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 70 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. Patients have cancer pain symptoms, confirmed by a physician as cancer pain or neuropathic cancer pain
  2. Experienced the worst pain NRS score ≥ 4
  3. The patient demonstrate good cognition and is able to cooperate with the assessment of pain severity.
  4. The estimated survival time exceeds 3 months.
  5. Pre-existing bisphosphonate, chemotherapy, and hormonal therapy regimens remained unchanged throughout the study.

Exclusion criteria

Exclusion Criteria:

  1. Individuals who have undergone head surgery or have metal implants in the head.
  2. Individuals with implanted cardiac pacemakers or cochlear prostheses.
  3. Have a history of epilepsy.
  4. Patients diagnosed with primary brain tumors or brain lesions.
  5. Present with additional neurological, psychiatric, or severe medical disorders.
  6. Individuals with metallic implants located in the cranial or cervical regions.
  7. Women who are pregnant.
  8. Presence of acute pain in any body region attributable to other medical conditions. -
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.

Metastases

Cancer that has spread from where it began to other parts of the body. “Metastatic” cancer is cancer that has spread this way.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
30 participants (estimated)

Study arms

  • Experimental
    Repetitive transcranial magnetic stimulation

    Device: Repetitive transcranial magnetic stimulation (rTMS)

  • Sham comparator
    Sham Repetitive transcranial magnetic stimulation

    Device: Repetitive transcranial magnetic stimulation (rTMS)

Interventions

  • DeviceRepetitive transcranial magnetic stimulation (rTMS)

    Repetitive transcranial magnetic stimulation toward for cancer pain (real and sham control)

06

What researchers measure

Primary outcomes

  1. Brief Pain Inventory, BPI

    BPI is to assess the severity of pain and the impact of pain on daily functions, including Severity of pain, impact of pain on daily function, location of pain, pain medications and amount of pain relief in the past 24 hours.

    Time frame: Assess the BPI outcome before the intervention, after 1 week and 2 weeks of intervention, as well as 1 week and 4 weeks after the intervention is completed.

  2. McGill Pain Questionnaire

    The McGill Pain Questionnaire (MPQ) is a self-report measure used by patients with various diagnoses to assess pain. It consists of 78 words, from which respondents select those that best describe their pain experience. The words are categorized as follows: Dimensions 1 to 10 (pain descriptors): 3 words Dimensions 11 to 15 (affective components of pain): 3 words Dimension 16 (evaluation of pain): 1 word Dimensions 17 to 20 (miscellaneous): 1 word. Scores are calculated by summing the values associated with each selected word, with scores ranging from 0 (no pain) to 78 (severe pain). Qualitative differences in pain are reflected in the respondent's word choices.

    Time frame: Assess MPQ scores before the intervention, after 1 week and 2 weeks of intervention, as well as 1 week and 4 weeks after the intervention is completed.

Secondary outcomes

  1. Numerical Rating Scale, NRS

    The Numeric Rating Scale (NRS) is commonly used to measure pain intensity and is well validated. It is scored from 0 to 10, with 0 representing no pain and 10 representing the worst pain imaginable

    Time frame: Assess the NRS scale before the intervention, after 1 week and 2 weeks of intervention, as well as 1 week and 4 weeks after the intervention is completed.

  2. Visual Analogue Scale , VAS

    The Visual Analog Scale (VAS) is a validated, subjective measure of both acute and chronic pain. Scores are recorded by making a handwritten mark on a 10-cm line that represents a continuum from 'no pain' to 'worst pain.'

    Time frame: Assess the VAS scale before the intervention, after 1 week and 2 weeks of intervention, as well as 1 week and 4 weeks after the intervention is completed.

  3. Resting-state functional imaging, rsfMRI

    In fMRI, by adding each pixel, the time course of a pixel is related to the average time course of the corresponding region of interest (ROI). In this context, the cross-correlation coefficient map for each seed ROI will be generated. This cross-correlation coefficient map will then undergo Fisher's z-transformation to approximate a normal distribution.

    Time frame: Assess the fMRI results before the intervention and after 2 weeks of interventions.

  4. Beck Depression Inventory, BDI

    BDI is a 21-item, self-report rating inventory that measures characteristic attitudes and symptoms of depression. Each answer is being scored on a scale value of 0 to 3. Higher total scores indicate more severe depressive symptoms.

    Time frame: Assess the BDI scale before the intervention, after 1 week and 2 weeks of intervention, as well as 1 week and 4 weeks after the intervention is completed.

  5. The 36-Item Short Form Survey quality of life

    The 36-Item Short Form Survey (It comprises 36 questions that cover eight domains of health) is an outcome measure instrument that is often used, well-researched, self-reported measure of health. It comprises 36 questions that cover eight domains of health.

    Time frame: Assess the The SF-36 outcome before the intervention, after 1 week and 2 weeks of intervention, as well as 1 week and 4 weeks after the intervention is completed.

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Study locations

1 site
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 18, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06949618
Lead sponsor
Taipei Medical University Hospital
Responsible party
Sponsor
First posted
Apr 29, 2025
Start date
May 20, 2025 (estimated)
Primary completion
Dec 16, 2026 (estimated)
Completion
Dec 30, 2026 (estimated)
Last update
May 18, 2025

Study contacts

Chien-Hung Lai, MD, PhD
Contact
chlai@tmu.edu.tw
+886227372181 ext. 3242

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Mar 2025. You cannot join it, but the record below documents what was studied.

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