MedPath

Breathing Techniques and Meditation for Health Care Workers During COVID-19 Pandemic

Phase 1
Active, not recruiting
Conditions
COVID-19 Infection
Interventions
Other: Media Intervention
Procedure: Meditation Therapy
Other: Quality-of-Life Assessment
Other: Questionnaire Administration
Procedure: Yoga
Registration Number
NCT04482647
Lead Sponsor
M.D. Anderson Cancer Center
Brief Summary

This phase I trial investigates breathing techniques and meditation for health care workers during COVID-19 pandemic. Breathing techniques and medication may help manage stress and improve lung health. The goal of this trial is to learn if breathing techniques and meditation may help to reduce stress and improve lung health in health care workers during the COVID-19 pandemic.

Detailed Description

PRIMARY OBJECTIVE:

I. To demonstrate the feasibility of a short pranayama or breathing techniques and meditation during Covid-19 pandemic.

SECONDARY OBJECTIVES:

I. To determine the adherence to the practice assessed as at least 50% of participants implement the intervention for 3 or more times in a week by the end of week 1/day 7 (+ 3 days).

II. To determine the change in resilience, perceived stress and psychological impact from day 0 today 28 as measured by the Brief Resilient Coping Scale (BRCS), Perceived Stress Scale (PSS4), and COVID-19 Stress among health care workers questionnaire.

III. To determine the changes in breath holding time measured weekly for 4 weeks.

IV. To determine the differences in breath holding time between those who are adherent and those who are not adherent to the practice.

OUTLINE:

Patients view an instructional video on breathing techniques and meditation. Patients then perform breathing techniques over 3 minutes and meditation over 2 minutes twice daily (BID) for 28 days.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
100
Inclusion Criteria
  • Participants must be able to read and understand English
  • Must be employed at MD Anderson Cancer Center
Read More
Exclusion Criteria
  • Epilepsy
  • Brain tumor
  • Brain aneurysm
  • Pregnant or trying to get pregnant
  • Brain bleeding in the past 1 year
  • Recent abdominal surgery and not cleared to exercise
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Supportive Care (video, breathing techniques, meditation)Quality-of-Life AssessmentPatients view an instructional video on breathing techniques and meditation. Patients then perform breathing techniques over 3 minutes and meditation over 2 minutes BID for 28 days.
Supportive Care (video, breathing techniques, meditation)Media InterventionPatients view an instructional video on breathing techniques and meditation. Patients then perform breathing techniques over 3 minutes and meditation over 2 minutes BID for 28 days.
Supportive Care (video, breathing techniques, meditation)Meditation TherapyPatients view an instructional video on breathing techniques and meditation. Patients then perform breathing techniques over 3 minutes and meditation over 2 minutes BID for 28 days.
Supportive Care (video, breathing techniques, meditation)Questionnaire AdministrationPatients view an instructional video on breathing techniques and meditation. Patients then perform breathing techniques over 3 minutes and meditation over 2 minutes BID for 28 days.
Supportive Care (video, breathing techniques, meditation)YogaPatients view an instructional video on breathing techniques and meditation. Patients then perform breathing techniques over 3 minutes and meditation over 2 minutes BID for 28 days.
Primary Outcome Measures
NameTimeMethod
Number of Participants Recruited to the Study (Feasibility)Within 2 months

To demonstrate the feasibility of a short pranayama or breathing techniques and meditation during Covid-19 pandemic. Feasibility will be defined as recruitment of 50 participants to the study within 2 months.

Number of Participants Who Perceived the Intervention as UsefulWeek 1 and Week 4

Defined as more than 50% of participants perceive the intervention as useful. Meditation perception questions were asked such as usefulness, feeling at peace, hopeful, or relaxed, and responses were recorded as strongly agree, agree, neutral, disagree, and strongly disagree at weeks 1 and 4.

Secondary Outcome Measures
NameTimeMethod
Change in Resilience4 weeks

Measured by the Brief Resilient Coping Scale among health care workers questionnaire.

Perceive Stress and Psychological Impact4 weeks

Measured by the Perceived Stress Scale and COVID-19 Stress among health care workers questionnaire.

Breath Holding Time4 weeks

Will determine the differences in breath holding time between those who are adherent and those who are not adherent to the practice.

Adherence to the Practice4 weeks

Will determine the adherence to the practice assessed as at least 50% of participants implement the intervention for 3 or more times in a week by the end of week 1/day 7 (+ 3 days).

Trial Locations

Locations (1)

M D Anderson Cancer Center

🇺🇸

Houston, Texas, United States

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