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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03292328
Other study ID # 17-449
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 18, 2017
Est. completion date September 15, 2020

Study information

Verified date September 2020
Source Memorial Sloan Kettering Cancer Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 51
Est. completion date September 15, 2020
Est. primary completion date September 15, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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/Exclusion Criteria

Inclusion Criteria:

- English speaking

- Age >/= 18 years old

- Survivors with a primary diagnosis of Stage I-III breast, ovarian, uterine, or endometrial cancer

- CIPN symptoms such as numbness, tingling, or pain ratings < 2 on a 0-10 NRS scale

- Have completed neurotoxic chemotherapy, i.e. taxanes (paclitaxel, docetaxel) and platinum (carboplatin) at least 3 months prior to enrollment

- ECOG performance status 0-2

Exclusion Criteria:

- Patients with metastatic disease

- Patients taking anti-neuropathy medication

- Patients who are currently receiving physical therapy or practicing yoga for any reason

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Yoga
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.
Wait List Control
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.

Locations

Country Name City State
United States Memoral Sloan Kettering Westchester Harrison New York
United States Memorial Sloan - Kettering Cancer Center New York New York

Sponsors (1)

Lead Sponsor Collaborator
Memorial Sloan Kettering Cancer Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in treatment related peripheral neuropathy symptoms Treatment related symptoms will be evaluated by using NCI CTCAE v4.0 8 weeks of the participants' most bothersome peripheral neuropathy symptom
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