ClinConnect ClinConnect Logo
Search / Trial NCT05121558

The Effect of Yoga on Nerve Pain Caused by Chemotherapy (Chemotherapy-Induced Peripheral Neuropathy)

Launched by DANA-FARBER CANCER INSTITUTE · Nov 4, 2021

Trial Information

Current as of July 22, 2025

Recruiting

Keywords

Yoga Chemotherapy Induced Peripheral Neuropathy Neuropathic Pain Pain Management Dana Farber Cancer Institute Memorial Sloan Kettering Cancer Center Cancer Survivor Cipn

ClinConnect Summary

This clinical trial is studying whether yoga can help reduce nerve pain caused by chemotherapy, a condition known as chemotherapy-induced peripheral neuropathy (CIPN). Participants in the study will be divided into three groups: one group will attend yoga classes, another will receive educational sessions about CIPN and how yoga might help, and the last group will receive standard care with medications for nerve pain. The researchers want to see how these different approaches impact balance, the risk of falling, and overall quality of life, as well as how yoga affects the feeling in the hands and feet.

To be eligible for this trial, participants must be at least 18 years old, speak English, and have experienced moderate to severe nerve pain from chemotherapy. They should have completed chemotherapy at least three months before joining the study and must not have received any physical therapy or practiced yoga for CIPN in the past three months. If you decide to participate, you can expect to be randomly assigned to one of the three groups and will need to follow certain guidelines, like not starting new pain medications during the first 12 weeks. This trial is currently recruiting participants, and it aims to find out if yoga can be a beneficial treatment option for those suffering from CIPN.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • English-proficient men and women aged ≥18 years
  • Free of oncologic disease or or stable disease by clinical examination and history
  • Completed neurotoxic chemotherapy such as platinum agents, taxanes, vinca alkaloids, and bortezomib at least three months prior to enrollment
  • Diagnosis of CIPN based on symptom history, loss of deep tendon reflexes, or the presence of symmetrical stocking-glove pain, numbness, or paresthesia Grade ≥1 sensory pain based on the NCI Common Terminology Criteria for Adverse Events (CTCAE) version 5.0
  • Self-reported moderate to severe CIPN pain, as defined by a score of 4 or greater on the BPI-SF average pain item over the past week
  • On a stable regimen (no change in three months) if taking anti-neuropathy or other pain medications and not taking acetyl-L-carnitine 77
  • Willing to adhere to requirement that no new pain medication be taken throughout the first 12 weeks of the study period
  • Willing to adhere to all study-related procedures, including randomization to one of the three arms
  • Patient answers "Yes" to at least one factor in the question: "Do you think your balance, gait, posture, alignment, or flexibility has been affected by your experience of CIPN?"
  • Exclusion Criteria:
  • Patients who have received physical therapy or practiced yoga for CIPN in the past 3 months. As patients who have received physical therapy or practiced yoga in this time period may already be experiencing its benefits, we will exclude such patients.

About Dana Farber Cancer Institute

The Dana-Farber Cancer Institute is a premier cancer research and treatment institution located in Boston, Massachusetts. Renowned for its commitment to advancing cancer care through innovative research, the institute integrates cutting-edge clinical trials with a multidisciplinary approach to patient care. With a focus on translating scientific discoveries into effective therapies, Dana-Farber collaborates with a network of leading researchers and healthcare professionals to improve outcomes for patients with cancer. The institute’s dedication to education, advocacy, and community engagement further underscores its mission to eradicate cancer and enhance the quality of life for those affected by the disease.

Locations

New York, New York, United States

Boston, Massachusetts, United States

Basking Ridge, New Jersey, United States

Middletown, New Jersey, United States

Montvale, New Jersey, United States

Harrison, New York, United States

Basking Ridge, New Jersey, United States

Rockville Centre, New York, United States

Commack, New York, United States

Patients applied

0 patients applied

Trial Officials

Ting Bao, MD

Principal Investigator

Dana-Farber Cancer Institute

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Similar Trials