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Yoga for Symptoms of Nerve Damage Caused by Chemotherapy

Yoga for Chemotherapy-Induced Peripheral Neuropathy in Breast and GYN Cancer Survivors: A Pilot Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03292328
Enrollment
51
Registered
2017-09-25
Start date
2017-09-18
Completion date
2020-09-15
Last updated
2025-05-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer, Peripheral Neuropathy, Gynecologic Cancer

Keywords

breast cancer, neuropathy, peripheral neuropathy, yoga, 17-449

Brief summary

Some types of chemotherapy used to treat breast cancer can cause damage to nerves with symptoms like tingling, numbness, muscle weakness, and pain in the hands and feet that can last and can affect functioning. The purpose of this study is to find out the effects of yoga on reducing symptoms caused by such nerve damage.

Interventions

OTHERYoga

Participants in the Yoga group will meet twice weekly for 8 weeks of classes taught by MSK yoga instructors. Each class will last for sixty minutes. In addition to these group classes, participants will utilize a home-based program on the days group classes are not held. The daily home practice will continue for four weeks after the group classes are finished.

Participants in the WLC group will continue usual care for twelve weeks before participating in Yoga classes for eight weeks. At the end of the twelve week follow-up, these subjects will receive eight weeks of group Yoga classes and the home Yoga practice recording. At week 20, they will complete a final follow-up visit.

Sponsors

Memorial Sloan Kettering Cancer Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* English-speaking * Age \>/= 18 years old * Survivors with a primary diagnosis of stage I-III breast, ovarian uterine, or endometrial cancer * Moderate to severe chemotherapy induced peripheral neuropathy, defined by symptoms such as numbness, tingling, or pain ratings of 4 or greater on a 0-10 numeric rating scale * Have completed neurotoxic chemotherapy, i.e. taxanes (paclitaxel, docetaxel) and platinum (carboplatin) at least 3 months prior to enrollment * If taking anti-neuropathy medications, they are on a stable regiment (no change in 3 months) * ECOG performance status 0-2

Exclusion criteria

* Participants with metastatic disease * Participants who are currently receiving physical therapy or practicing yoga for any reason Control Group - Inclusion/

Design outcomes

Primary

MeasureTime frameDescription
Change in treatment related peripheral neuropathy symptoms8 weeks of the participants' most bothersome peripheral neuropathy symptomTreatment related symptoms will be evaluated by using NCI CTCAE v4.0

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026