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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03262831
Other study ID # 201708076
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 10, 2018
Est. completion date June 26, 2019

Study information

Verified date August 2019
Source Washington University School of Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators hypothesize that a personalized yoga program with mindful movement implemented during breast cancer therapy will benefit women in multiple ways. The investigators predict that women participating in the program will experience less weight gain and fatigue and will have an improved quality of life compared to women not participating in the program. The investigators predict that this will be associated with decreased markers of inflammation. The investigators will also evaluate whether there is improved pathologic response rate compared to historical controls. This study will provide pilot data for a larger randomized controlled trial assessing whether program can provide long-term improvement in quality of life, weight maintenance, and the serum and tumor changes correlating with a reduced risk of recurrence and mortality.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date June 26, 2019
Est. primary completion date June 26, 2019
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Eligibility Critera:

- Age = 18.

- Female.

- Newly diagnosed with Stage I-III breast cancer.

- Scheduled to undergo neoadjuvant or adjuvant chemotherapy or neoadjuvant endocrine therapy.

- Not currently regularly practicing yoga (defined as at least once a month).

- Able to read and understand English

- Able to understand and willing to sign an IRB-approved written informed consent document

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Yoga
The yoga practice, Gentle Hatha and Restorative Yoga, will be based on protocols that have been found to decease fatigue and weight gain by helping the participant gain insight in recognizing stress responses and ways to relax
Procedure:
Blood draw
Baseline and end of treatment To evaluate change in inflammatory markers (CRP, IL-6, and TNF)
Behavioral:
FACT-G questionnaire
7 statements that other people with breast cancer have said are important, the patient is to circle or mark one number per line to indicate the response as it applies in the last 7 days Answers range from 0=not at all to 4=very much
Procedure:
Weight measurement
-Weight will be taken at baseline, on day 1 of each cycle, and the end of treatment
Behavioral:
Recent Physical Activity Questionnaire
-To assess physical activity, the RPAQ will be completed at baseline and at the end of treatment.
NHANES Food Questionnaire
-To assess diet, the NHANES Food Questionnaire will be completed at baseline and at the end of treatment.

Locations

Country Name City State
United States Washington University School of Medicine Saint Louis Missouri

Sponsors (2)

Lead Sponsor Collaborator
Washington University School of Medicine BJH Foundation

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Feasibility of enrolling patients to larger randomized controlled trial using yoga and mindful movement as measured the number of eligible patients enrolled -Feasibility is defined as the ability to enroll 60% of eligible patients Completion of study enrollment (estimated to be 6 months)
Primary Feasibility of conducting a larger randomized trial using yoga and mindful movement -Feasibility is defined as the ability to have an 80% completion rate of the intervention Completion of study enrollment (estimated to be 6 months)
Primary Efficacy of yoga exercise as measured by weight change from baseline to completion Completion of treatment (estimated to be 6 months)
Secondary Effect of yoga exercise as measured by rate of pathologic response (partial and complete) (neoadjuvant subset only) Completion of treatment (estimated to be 6 months)
Secondary Effect of yoga exercise as measured by inflammatory markers Completion of treatment (estimated to be 6 months)
Secondary Effect of yoga exercise as measured by fatigue index -Fatigue index will be measured by FACT-G questionnaire Completion of treatment (estimated to be 6 months)
Secondary Effect of yoga exercise as measured by quality of life -Quality of life will be measured by FACT-G questionnaire Completion of treatment (estimated to be 6 months)
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