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Effects of Emotional Stimulation on the Stress Levels of Healthy Persons

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01187797
First Posted: August 24, 2010
Last Update Posted: October 25, 2010
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:
Charite University, Berlin, Germany
  Purpose
The purpose of this study is to evaluate the effects of a short-term emotional stimulation on the mood of healthy persons.

Condition Intervention Phase
Depression Somatization Disorder Anger Anxiety Other: Emotional stimulation Phase 1 Phase 2

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Evaluation of the Effects of a Body-centered Emotional Stimulation in Healthy Persons

Further study details as provided by Charite University, Berlin, Germany:

Primary Outcome Measures:
  • Depression [ Time Frame: After 10 days ]
    Depression scores will be evaluated with the BDI

  • Somatization [ Time Frame: After 10 days ]
    Somatization will be assessed with the SOMS7 questionnaire


Enrollment: 21
Study Start Date: August 2010
Study Completion Date: September 2010
Primary Completion Date: September 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Intervention Other: Emotional stimulation
Increase of the physical correlates of an emotion

Detailed Description:
The trial assesses the effects of a emotion-centered stimulation on the mood of healthy persons. The outcomes will be evaluated with standard questionnaires.
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 45 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Age 18 to 45
  • Ability to speak German

Exclusion Criteria:

  • Physical or psychiatric disorders
  • Consume of drugs or alcohol 24 previous to the test
  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): NCT01187797


Locations
Germany
Charité Universitätsmedizin Berlin
Berlin, Germany, 12200
Sponsors and Collaborators
Charite University, Berlin, Germany
Investigators
Principal Investigator: fernando Dimeo, MD Charite University, Berlin, Germany
  More Information

Responsible Party: Fernando Dimeo, Charie Universitätsmedizin Berlin
ClinicalTrials.gov Identifier: NCT01187797     History of Changes
Other Study ID Numbers: EA408109
First Submitted: August 9, 2010
First Posted: August 24, 2010
Last Update Posted: October 25, 2010
Last Verified: August 2010

Additional relevant MeSH terms:
Somatoform Disorders
Mental Disorders