This trial studies how well meditative slow breathing or Isha Kriya meditation works in improving cancer-related symptoms in hospitalized participants with cancer. Meditative slow breathing or Isha Kriya meditation may help to decrease perceived stress and enhance well-being in hospitalized cancer participants.
PRIMARY OBJECTIVES: I. Test the feasibility of the meditation practice. SECONDARY OBJECTIVES: I. Explore the acceptability of meditation in cancer patients through modified Global Symptom Evaluation (GSE) and on day 7 +/- 1 day and day 28 +/- 3 days. II. Explore the effect of meditative practices in cancer patients through Edmonton Symptom Assessment Scale (ESAS) on the day of enrolment and a weekly basis until the end of study at four weeks. OUTLINE: Participants are randomized to 1 of 3 groups. GROUP I (MSB): Participants are instructed on the meditative slow breathing (MSB) technique and then perform MSB over 15 minutes twice daily (BID) for 28 days. GROUP II (IK MEDITATION): Participants are instructed on the 3 steps of Isha Kriya (IK) meditation and then perform IK meditation over 15 minutes BID for 28 days. GROUP III (WAITLIST): Participants are placed on a waitlist and receive standard supportive care for 28 days. After 28 days, participants may crossover to Group II.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Enrollment
41
Receive standard supportive care
Perform MSB
Perform IK meditation
M D Anderson Cancer Center
Houston, Texas, United States
Feasibility of the Meditation Practice defined by Recruitment Rate
Time frame: Day 7
Feasibility of the Meditation Practice defined by Adherence Rate
Time frame: Day 7
Acceptability of Meditation in Cancer Patients Assessed by Modified Global Symptom Evaluation (GSE)
Time frame: Day 7 and Day 28
Effect of Meditative Practices in Cancer Patients Assessed by Edmonton Symptom Assessment Scale (ESAS)
Scale is from 0 to 10 with 0 being no symptoms to 10 being worse symptoms. Proportions of participants who consider that the study makes their symptoms better estimated along with a 90% confidence interval for each of the intervention groups. The Linear mixed model used to examine the differential changes over time for ESAS scores among the three groups.
Time frame: Enrollment and a weekly basis until the end of study at four weeks.
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