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NCT00369902 Clinical Trial

The Effect of Acupuncture Treatment on the Perception of Pain and Coping With Pain

Pain Clinical Trial

Official title:
Pilot Study on the Effect of Acupuncture Treatment on Pain Perception and on the Ability to Cope With Pain

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00369902
Other study ID # SHEBA-05-3817-OG-CTIL
Secondary ID
Status Completed
Phase N/A
First received August 29, 2006
Last updated July 19, 2009
Start date May 2006
Est. completion date May 2007

Study information
Verified date July 2009
Source Sheba Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Observational

Clinical Trial Summary

The Purpose of this study is to evaluate whether cognitive and emotional components take part in the positive acupuncture effect on pain.

Description:

The effect of acupuncture on pain intensity has been already investigated and confirmed. Recent publication (Pariente J., et a., 2005) indicated that acupuncture may affect midbrain areas, that are associated with cognitive control of pain.

The Pain Self Regulation Model (Levental, 1980)distinguishes between emotional response pain representations and cognitive pain representations. According to this model, emotional and cognitive pain representations leads to a new (cognitive or emotional) evaluation of the pain, that affects its perception and the ability to cope with it (Levental at al., 2001).

This study will try to assess the hypothesis that acupuncture treatment is involved in this process.

The study is designed as pilot study, limited to 45 patients.

Recruitment information / eligibility
Status Completed
Enrollment 41
Est. completion date May 2007
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- patients suffering from pain,who are reffered for acupuncture treatment,and consented to participate in this study

Exclusion Criteria:

- children under 18 years of age

Study Design

Observational Model: Case-Only, Time Perspective: Prospective

Related Conditions & MeSH terms

Intervention

Procedure:
• acupuncture

Locations
Country Name City State
Israel Sheba Hospital, Ramat Gan

Sponsors (2)
Lead Sponsor Collaborator
Sheba Medical Center Assaf-Harofeh Medical Center

Country where clinical trial is conducted

Israel, 

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