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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01428674
Other study ID # IRB00015699
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 2011
Est. completion date June 2011

Study information

Verified date August 2018
Source Wake Forest University Health Sciences
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to describe the onset, duration and dose-response of interpersonal mindful compassion on respiratory rate and heart rate variability in healthy adults in order to prepare for research evaluating the impact of this intervention in patient populations and to prepare for basic research investigating the CNS mechanisms for observed effects.

Previous research has found that mindfulness meditation, including mindful compassion, results in autonomic changes in the practitioner. Emerging neuroscience of dyadic interactions suggests that through the effects of mirror neuron isopraxis, one person's physiologic state may be mirrored by another. However, no research has directly evaluated the impact of one person's mindful compassion on another person's autonomic activity. This study paves the way for an entirely new avenue of research inquiry.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date June 2011
Est. primary completion date June 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- Healthy subjects age 18 - 40

Exclusion Criteria:

- Taking beta blocker medication

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Interpersonal Mindful Compassion with Touch
A practitioner lightly touches the participant on the hands, arms, shoulders, lower legs and feet while extending loving kindness to the participant.
Reading while extending loving kindness
The practitioner sits in a room with the participant, pretending to read, while extending loving kindness to the participant.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Wake Forest University

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Heart Rate Variability from pre-intervention period to intervention period continuous monitoring for 10 min before intervention and during 10 or 20 minute intervention
Primary Change in Respiratory Rate from pre-intervention period to intervention period continuous monitoring for 10 minutes before intervention and during 10 or 20 minute intervention
Secondary Perceived Stress, Relaxation, Peacefulness baseline, after a 10 minute rest period, before 10 or 20 minute intervention, immediately after intervention, 20 minutes after intervention
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