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RecruitingNCT07177820Updated Jul 22, 2026

VGAIT for Chemotherapy-induced Peripheral Neuropathy

An interventional study of Video-Guided Acupuncture Imagery Treatment (VGAIT) in Chemotherapy-induced Peripheral Neuropathy, sponsored by Massachusetts General Hospital. Recruiting at 1 site in United States. Open to female participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-07-22.

Sponsored by Massachusetts General Hospital · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Started Jan 2026; still recruiting 9 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Not applicable
Ages
18 Years to 80 Years
Sex
Female
01

Study summary

Perform a feasibility study on imagined acupuncture treatment of Chemotherapy-induced peripheral neuropathy (CIPN)

Read the detailed description

We will perform a pilot study to assess the feasibility of Video-Guided Acupuncture Imagery Treatment (VGAIT) on CIPN symptoms in patients with stage I-III breast cancer with persistent CIPN after adjuvant chemotherapy. Participants will receive 16 sessions of VGAIT over 8 weeks remotely through the zoom. Study measures will be collected at the time of study enrollment, week 4, and week 8. The primary endpoints of the study will be 1) retention to treatment; 2) satisfaction for the intervention and 3) completion of study assessments.

02

Conditions studied

  • Chemotherapy-induced Peripheral Neuropathy
03

In context

Lead sponsor

Massachusetts General Hospital is the lead sponsor of 2,536 studies on the registry; 446 are open to participants now.

Of its 214 completed or terminated interventional studies of FDA-regulated products, 161 (75%) have results posted.

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

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  • at least 18 years of age
  • have histologically confirmed stage I-III breast cancer,
  • have completed adjuvant taxane-based chemotherapy (alone or in combination), ,
  • have an Eastern Cooperative Oncology Group performance status of 0 or 1, and reported grade 1 or greater CIPN symptoms for more than 2 weeks as defined by the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE), version 4.03.

Exclusion criteria

Exclusion Criteria:

  • concurrent chemotherapy (there were no limitations on time from the last paclitaxel administration),
  • having metastatic or recurrent disease,
  • history of preexisting peripheral neuropathy prior to chemotherapy,
  • uncontrolled seizure disorder,
  • unstable cardiac disease or myocardial infarction within 6 months prior to study entry, being pregnant or nursing, or having used acupuncture for CIPN within 6 months prior to study entry.
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
20 participants (estimated)

Study arms

  • Experimental
    VGAIT

    Other: Video-Guided Acupuncture Imagery Treatment (VGAIT)

Interventions

  • OtherVideo-Guided Acupuncture Imagery Treatment (VGAIT)

    Participants watch a video of acupuncture being applied to the body while simultaneously imagining that it is being administered to them

06

What researchers measure

Primary outcomes

  1. Feasibility related outcomes

    Completion, satisfaction

    Time frame: 8 week

Secondary outcomes

  1. Patient Neurotoxicity Questionnaire (PNQ)

    A tool designed to assess neurotoxic effects in patients who have undergone treatments such as chemotherapy

    Time frame: baseline, 8 week

  2. Functional Assessment of Cancer Therapy-Neurotoxicity subscale (FACT-NTX)

    a widely used, validated instrument that assesses the impact of neuropathy on health-related quality of life

    Time frame: baseline, 8 week

  3. Brief Pain Inventory-short form (BPI-SF)

    An instrument used to evaluate the severity of pain, including neuropathic pain, and the impact on the patient's daily functioning.

    Time frame: baseline, 8 week

  4. European Organisation for Research and Treatment of Cancer Quality-of-Life Questionnaire Core 30 (QLQ-C30) instrument

    an instrument developed to assess the quality of life in cancer patients

    Time frame: baseline, 8 week

  5. MGH Acupuncture Sensation Scale (MASS)

    scale includes 12 descriptors of sensations frequently described during acupuncture treatment

    Time frame: after each intervention

  6. Pain Catastrophizing Scale (PCS)

    a 13-item self-report scale which measures pain-related rumination, magnification, and helplessness

    Time frame: baseline, 8 week

07

Study locations

1 of 1 sites recruiting
  • Massachusetts General Hospital
    Charlestown, Massachusetts 02129, United States
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 22, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07177820
Lead sponsor
Massachusetts General Hospital
Responsible party
Jian Kong (Professor, Massachusetts General Hospital) — Principal investigator
First posted
Sep 17, 2025
Start date
Jan 6, 2026
Primary completion
Dec 1, 2026 (estimated)
Completion
Dec 31, 2026 (estimated)
Last update
Jul 22, 2026

Study contacts

Sierra Hodges
Contact
sahodges@mgb.org
6177265004
Jian Kong
Contact
jkong2@mgh.harvard.edu
16179620978

Oversight

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

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