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Muscle Relaxation Therapy With Odorant Cue

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00208910
First Posted: September 21, 2005
Last Update Posted: November 11, 2013
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Emory University
  Purpose
A novel procedure for generalized anxiety disorder where an odorant cue is paired with the state of deep relaxation during training. It is hypothesized that by smelling the odor in an anxiety-provoking situation, the patient will more easily invoke a state of relaxation, providing greater relief from the distressing tension and worry that characterize GAD.

Condition Intervention
Generalized Anxiety Disorder Anxiety Behavioral: Odorant Cue

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: Single
Primary Purpose: Treatment
Official Title: A Study of Enhancement of Progressive Muscle Relaxation Therapy for Generalized Anxiety Disorder Through Use Of An Odorant Cue.

Resource links provided by NLM:


Further study details as provided by Emory University:

Primary Outcome Measures:
  • PSWQ

Secondary Outcome Measures:
  • HAM-A

Estimated Enrollment: 15
Study Start Date: November 2003
Estimated Study Completion Date: May 2005
Detailed Description:
We hypothesize that by presenting a novel odor to a patient in a state of deep relaxation, the odor will serve as a conditioned inhibitory stimulus, or safety signal, in anxiety-provoking situations. With the odor serving as a contextual cue for the state of relaxation.
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 65 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • GAD without a comorbid active major psychiatric disorder.
  • GAD must be the primary active psychiatric disorder.
  • GAD determined via the Mini International Neuropsychiatric Interview (MINI).

Exclusion Criteria:

  • Significant medical illness that might interfere with the relaxation therapy or with training using the odorant.
  • Actively abusing alcohol.
  • Illicit substances.
  • Currently using rapid-acting anxiolytic agents (e.g. benzodiazepines, hydroxyzine).
  • Started an antidepressant, antipsychotic or mood stabilizing agent within three months of screening visit.
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00208910


Locations
United States, Georgia
Emory University School of Medicine
Atlanta, Georgia, United States, 30329
Sponsors and Collaborators
Emory University
Investigators
Principal Investigator: Philip T Ninan, MD Emory University
  More Information

ClinicalTrials.gov Identifier: NCT00208910     History of Changes
Other Study ID Numbers: 0860-2003
First Submitted: September 13, 2005
First Posted: September 21, 2005
Last Update Posted: November 11, 2013
Last Verified: November 2013

Keywords provided by Emory University:
Anxiety
Mental Health

Additional relevant MeSH terms:
Anxiety Disorders
Mental Disorders


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