Clinical trial Recruiting at 1 site Interventional Ages 18 to 80 Women only

Video-guided imagined acupuncture for chemotherapy-related nerve pain

Official title: Video-Guided Acupuncture Imagery Treatment in Chemotherapy-induced Peripheral Neuropathy

Run by Massachusetts General Hospital · NCT07177820 · Data updated 2026-11-12

This program will try a video-guided imagined acupuncture (VGAIT) approach to help people with ongoing nerve pain after taxane chemotherapy for early-stage breast cancer.

More Chemotherapy-induced Peripheral Neuropathy trials

Quick facts

Study typeInterventional
Ages18 Years to 80 Years
SexWomen only
Enrollment20 (estimated)
SponsorMassachusetts General Hospital
Academic / other
Drugs / interventionschemotherapy
Locations1 site (Charlestown, Massachusetts)
StatusRecruiting
StartedJanuary 6, 2026
Main results expectedDecember 1, 2026
Study endsDecember 31, 2026
Registry record updatedJuly 22, 2026
Trial IDNCT07177820 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (≥18 years) with histologically confirmed stage I–III breast cancer who completed adjuvant taxane-based chemotherapy, have persistent grade ≥1 CIPN for more than two weeks, and have ECOG performance status 0–1 are ideal candidates.

Probably not a fit

People with metastatic or recurrent disease, preexisting neuropathy prior to chemotherapy, uncontrolled seizure disorder, unstable cardiac disease or recent myocardial infarction, current pregnancy or nursing, concurrent chemotherapy, or recent acupuncture for CIPN are unlikely to benefit or be eligible.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This pilot feasibility intervention will deliver 16 remote sessions of Video-Guided Acupuncture Imagery Treatment (VGAIT) over eight weeks to adults with stage I–III breast cancer who have persistent chemotherapy-induced peripheral neuropathy after taxane-based adjuvant chemotherapy. Sessions are conducted via Zoom and study measures are collected at enrollment, week 4, and week 8. The primary endpoints are retention to treatment, participant satisfaction with the intervention, and completion of study assessments. Findings will inform whether a larger efficacy trial of VGAIT for CIPN is feasible.

Why it matters

Potential benefit: If successful, VGAIT could provide a noninvasive, remotely delivered option to reduce CIPN symptoms and improve quality of life.

How similar studies have gone: Imagery-based acupuncture and other mind–body interventions have shown limited promise in small pain studies, but VGAIT specifically for CIPN is a novel and minimally tested approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
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:

* 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.

Where it's running

  • Massachusetts General Hospital
    Charlestown, Massachusetts, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.