Molecular Processes of the Relaxation Response in Older Adults
NCT ID: NCT00179569
Last Updated: 2007-11-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE2
40 participants
INTERVENTIONAL
2005-08-31
2007-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
SINGLE_GROUP
TREATMENT
NONE
Interventions
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Relaxation response
8 weeks of relaxation response training
Eligibility Criteria
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Inclusion Criteria
* healthy individuals
* willing and able to attend treatment sessions
* willing to learn how to do and practice the relaxation-response
* access to a working telephone
* read and write English
Exclusion Criteria
* asthma or seasonal allergies (resulting in nitric oxide levels \>60 ppb)
* smoking
* previous relaxation-response practice
* current use of the following medications:systemic corticosteroids, anti-convulsants/psychotics, immunosuppressants, cytotoxic therapy, anabolic steroids, antidepressants (other than SSRIs), dicyclomine, bile acid binding resins, or sympathomimetic medication
60 Years
80 Years
ALL
Yes
Sponsors
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Centers for Disease Control and Prevention
FED
Beth Israel Deaconess Medical Center
OTHER
Principal Investigators
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Jeffery A Dusek, PhD
Role: PRINCIPAL_INVESTIGATOR
Beth Israel Deaconess Medical Center
Locations
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BIDMC
Boston, Massachusetts, United States
Countries
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Other Identifiers
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H75-CCH-123424
Identifier Type: -
Identifier Source: secondary_id
H75-CCH-119124
Identifier Type: -
Identifier Source: secondary_id
2004P-000418
Identifier Type: -
Identifier Source: org_study_id