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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01351402
Other study ID # 00012002
Secondary ID
Status Completed
Phase N/A
First received May 6, 2011
Last updated May 9, 2011
Start date June 2006
Est. completion date January 2007

Study information

Verified date August 2005
Source Claremont Graduate University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

This study will investigate the effects of 15 minutes of massage compared to 15 minutes of quiet rest on physiological variables. Specifically, the investigators will measure the effects on levels of the social hormone oxytocin, and on other physiological variables that interact with oxytocin or that may be influenced by massage (including ACTH, Beta-endorphin, and IL-1alpha). The investigators will also investigate whether, in the case of hormones changes, these influence social decision making.


Description:

Interested participants will have the experiment explained both verbally and in writing, and asked to give their informed consent in writing. After consent, the participants will be led to a private room for their first 30ml blood draw by a qualified phlebotomist. Participants will then have a second 30ml blood draw.


Recruitment information / eligibility

Status Completed
Enrollment 95
Est. completion date January 2007
Est. primary completion date August 2006
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Anyone English speaking and over the age of 18.

Exclusion Criteria:

- Minors and anyone who has used illicit drugs or alcohol in the last 24 hours.

Study Design

Allocation: Randomized, Masking: Single Blind, Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Procedure:
Massage or Rest
Participants either received 15 minutes of moderate pressure Swedish massage on the upper back, or rested quietly sitting in a chair for 15 minutes.

Locations

Country Name City State
United States Cassel, UCLA Los Angeles California

Sponsors (2)

Lead Sponsor Collaborator
Claremont Graduate University Gruter Institute

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Oxytocin Participants receive a blood draw at baseline and immediately following 15 minutes of massage or rest and oxytocin will be measured from this sample. Within 5 minutes following experimental manipulation of either 15 minutes massage or rest. No
Secondary Adrenocorticotrophic hormone (ACTH) Participants will receive a blood draw at baseline and immediately following 15 minutes of massage or rest, and ACTH will be measured in these blood samples. Within 5 minutes following experimental manipulation of either 15 minutes massage or rest.
Secondary Beta-endorphin Participants will receive a blood draw at baseline and immediately following 15 minutes of massage or rest, and B-endorphin will be measured from these samples. Within 5 minutes following experimental manipulation of either 15 minutes massage or rest.
Secondary Interleukin-1alpha (IL-1a) Participants will receive a blood draw at baseline and immediately following 15 minutes of massage or rest, and IL-1a will be measured from these samples. Within 5 minutes following experimental manipulation of either 15 minutes massage or rest.
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