Yoga for Solid Tumor
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT03728205|
Recruitment Status : Withdrawn (Covid-19)
First Posted : November 2, 2018
Last Update Posted : April 27, 2021
|Condition or disease||Intervention/treatment||Phase|
|Solid Tumor, Adult||Behavioral: Yoga||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||0 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Primary Purpose:||Supportive Care|
|Official Title:||A Pilot Study On The Effect Of Yoga On Fatigue, And Stress Levels In Solid Tumor Cancer Patients Undergoing Active Radiation Therapy|
|Actual Study Start Date :||December 15, 2018|
|Actual Primary Completion Date :||December 31, 2020|
|Actual Study Completion Date :||January 14, 2021|
All 10 pilot subjects will be taking yoga
Twice weekly yoga sessions for 12 weeks
- The feasibility of implementing Eischens yoga interventions for solid tumor cancer patients undergoing radiation therapy. This will be measured by the success rate of recruitment and retention for 10 subjects. [ Time Frame: 12 months ]Feasibility
- Effects on fatigue [ Time Frame: 12 months ]Examine the effect of yoga on cancer and radiation related fatigue during radiation therapy. We will use the BFI results both before, during and after radiation therapy.
- Effects on Stress Level [ Time Frame: 12 Months ]Examine the effect of yoga on cancer and radiation related fatigue during radiation therapy. We will use the NCCN Distress thermometer results both before, during and after radiation therapy.
- Long Term [ Time Frame: 17 months ]Examine the long term effect of yoga to be tested at the 6 months post radiation visit. We will use the BFI and distress thermometer to see if any positive results during yoga are sustained to the 6 month follow up visit.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03728205
|United States, Pennsylvania|
|University of Pennsylvania|
|Philadelphia, Pennsylvania, United States, 19104|