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Does the Relaxation Response Inhibit Acute Stress?

Does the Relaxation Response Inhibit Acute Stress?

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00179595
Enrollment
140
Registered
2005-09-16
Start date
2002-05-31
Completion date
2011-10-31
Last updated
2017-02-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Keywords

nitric oxide, volumetric oxygen consumption

Brief summary

The purposes of this study are: 1. To examine molecular and biochemical changes, associated with the relaxation response (RR) that can counteract the effects of stress in healthy adults. 2. To compare genomic, molecular and biochemical parameters between healthy adults with a long term meditative practice and those with no experience in meditation. Since stress is a factor in the development of many health conditions, a further understanding of the mechanisms of the RR should be developed. The project is designed to determine how the RR can improve the quality of life that has been adversely affected by stress.

Detailed description

The purposes of this study are: 1. To examine molecular and biochemical changes, associated with the relaxation response (RR) that can counteract the effects of stress in healthy adults. 2. To compare genomic, molecular and biochemical parameters between healthy adults with a long term meditative practice and those with no experience in meditation. Since stress is a factor in the development of many health conditions, a further understanding of the mechanisms of the RR should be developed. The project is designed to determine how the RR can improve the quality of life that has been adversely affected by stress.

Interventions

BEHAVIORALrelaxation response- meditation

Sponsors

Centers for Disease Control and Prevention
CollaboratorFED
Beth Israel Deaconess Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to 49 Years
Healthy volunteers
Yes

Inclusion criteria

* healthy individual * age:18-49 years * able to read and understand English * able to attend al study visits * access to a telephone (to schedule visits)

Exclusion criteria

* current smoking * asthma * current use of any prescription or psychoactive medications or supplements * either: 1. no prior experience with RR eliciting techniques 2. at least 3 years of regular RR elicitation (at least 20 min/day) * BMI \>30 * exhaled nitric oxide levels \>60 ppb * abnormal lab values (Hct \<32,creatinine \>1.3, glucose \>200 * pregnancy

Design outcomes

Primary

MeasureTime frame
To examine molecular and biochemical changes, associated with the relaxation response (RR) that can counteract the effects of stress in healthy adults.

Secondary

MeasureTime frame
To compare genomic, molecular and biochemical parameters between healthy adults with a long term meditative practice and those with no experience in meditation.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026