MedPath

Psychological and Physiological Effects of Different Objects of Breath Meditation

Not Applicable
Completed
Conditions
Physiological Stress
Emotions
Psychological Stress
Interventions
Behavioral: Nostril focus followed by belly focus
Behavioral: Belly focus followed by nostril focus
Registration Number
NCT06051500
Lead Sponsor
University of Wisconsin, Madison
Brief Summary

The goal of this research is to test whether certain areas of focus in breath meditation are connected with certain mental health outcomes. The main question to be addressed is whether attention placed on the breath in the belly versus the nostrils during meditation results in differences in subjective experience, respiration and heart rate.

Participants will:

* complete surveys

* have heart rate and respiration measured

* practice focused breathing

Participants can expect the study visit to last for one hour.

Detailed Description

An online prescreen will determine eligibility. Participants that 1) are under 18, 2) are not students currently enrolled at UW-Madison 3) have previous mediation experience 4) obtain a high PROMIS depression or anxiety score, or 5) have been diagnosed with one or more psychiatric disorders by a healthcare professional that will be listed in the pre-screen survey will be excluded.

Participants deemed eligible following prescreen will schedule a lab visit. At the beginning of the lab visit, participants will be provided a consent document and time to ask questions. After signing the consent form, researchers will place ECG leads and a respiration belt on participants, and then complete the baseline survey battery. Participants will then sit at rest for 5 minutes of baseline heart rate and respiration data collection. Next, participants will be randomly assigned in a counterbalanced order to nostril focus first or belly focus first and asked to follow a brief (\~5 minute) guided practice. After the practice, participants will complete a second battery of self-reports and then have a 10-minute period of rest/recovery. They will then complete the second practice (\~5 minutes) followed by a final survey. The entire session will take about an hour.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
96
Inclusion Criteria
  • at least 18 years of age
  • student at UW Madison
  • no major history of meditation practice
Exclusion Criteria
  • under 18 years of age
  • not currently enrolled at UW Madison
  • have previous meditation experience
  • Self-reports a mental health diagnosis

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Nostril focus followed by belly focusNostril focus followed by belly focusParticipants will be randomly assigned to concentrate on the nostrils first, then the belly second following a period of rest.
Belly focus followed by nostril focusBelly focus followed by nostril focusParticipants will be randomly assigned to concentrate on the belly first, then the nostrils second following a period of rest.
Primary Outcome Measures
NameTimeMethod
Change in Positive and Negative Affect Schedule (PANAS-SF)At baseline; after meditation 1 (5 minutes); and, after meditation 2 (15 minutes)

PANAS-SF is a 20-item questionnaire to assess positive versus negative affect. 10 of the items indicate positive affect, 10 indicate negative. Scores can range between 10-50 for positive affect, with higher scores representing higher levels of positive affect. Scores can range between 10-50 for negative affect, with lower scores representing lower levels of negative affect.

Change in Heart RateBaseline to practice 1 epoch (10 minutes); baseline 2 to practice 2 epoch (25minutes)

Using ECG electrodes and a BIOPAC system, heart rate will be monitored. Paired with respiration rate, this will give us further insight into the physiological responses to the participant's experience of the two variations of breath meditation.

Change in RespirationBaseline to practice 1 epoch (10 minutes); baseline 2 to practice 2 epoch (25minutes)

Using respiration belts, rate of respiration will be collected. Paired with heart rate, this will give us further insight into the physiological responses to the participant's experience of the two variations of breath meditation.

Secondary Outcome Measures
NameTimeMethod
Perseverative Thinking (PTQ)Baseline only

The PTQ is a 15-item questionnaire asking how participants typically think about negative experiences or problems. Scores can range from 0-60, with higher scores representing higher levels of perseverative thinking.

Change in RelaxationAt baseline; after meditation 1 (5 minutes); and, after meditation 2 (15 minutes)

A research assistant or I will ask each participant to respond to the following statement: "In this moment I feel relaxed." Participants will select one of the following responses: strongly disagree, slightly disagree, neither agree nor disagree, slightly agree, strongly agree.

Change in FocusAt baseline; after meditation 1 (5 minutes); and, after meditation 2 (15 minutes)

A research assistant or I will ask each participant to respond to the following statement: "In this moment I feel focused." Participants will select one of the following responses: strongly disagree, slightly disagree, neither agree nor disagree, slightly agree, strongly agree.

Change in Interoceptive AwarenessAt baseline; after meditation 1 (5 minutes); and, after meditation 2 (15 minutes)

The Multidimensional Assessment of Interoceptive Awareness (MAIA) is a 37-item questionnaire that measures multiple dimensions of self-awareness. The Noticing, Attention Regulation and Self-regulation scales will be used. Scores range between from 0-20, 0-35 and 0-20, respectively, with higher scores represent higher interoceptive awareness.

Change in MindfulnessAt baseline; after meditation 1 (5 minutes); and, after meditation 2 (15 minutes)

The Five Facet Mindfulness Questionnaire (FFMQ) is a 39-item questionnaire. The Non-react to inner experience and Act with awareness subscales will be used. Scores can range from 7-35 and 8-40, respectively; higher scores represent higher levels of mindfulness facet.

Trial Locations

Locations (1)

University of Wisconsin

🇺🇸

Madison, Wisconsin, United States

© Copyright 2025. All Rights Reserved by MedPath