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NCT01869140 Clinical Trial

the Hypoalgesic Effect of Spinal Manual Therapy

Back Pain Clinical Trial

Official title:
the Hypoalgesic Effect of Spinal Manual Therapy on an Healthy Population: a Randomized Clinical Trial

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT01869140
Other study ID # IFEC-001
Secondary ID
Status Not yet recruiting
Phase N/A
First received May 17, 2013
Last updated October 4, 2013
Start date November 2013
Est. completion date May 2014

Study information
Verified date October 2013
Source Institut Franco Europeen de Chiropratique
Contact n/a
Is FDA regulated No
Health authority France: Ministère de l'Enseignement supérieur et de la Recherche
Study type Interventional

Clinical Trial Summary

To study the immediate effect of spinal manual therapy on pain perception in normal subjects

Description:

Is this effect only local or is it also noticed away from the stimulated area? How long does it last? Is there a dose/response phenomenon?

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 90
Est. completion date May 2014
Est. primary completion date May 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

Healthy Students who volunteer from Murdoch University

Exclusion Criteria:

- contraindication to spinal manual therapy

Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Basic Science

Related Conditions & MeSH terms

Intervention

Device:
• spinal manual therapy
spinal manipulation either manual or instrumental (activator)

Locations
Country Name City State
Australia Murdoch University Perth Western Australia

Sponsors (1)
Lead Sponsor Collaborator
Institut Franco Europeen de Chiropratique

Country where clinical trial is conducted

Australia, 

Outcome
Type Measure Description Time frame Safety issue
Primary the Pressure pain threshold in KPa/Cm2 will be measure with an Algometer (SOMEDIC) the pressure pain threshold will be measure immediately after intervention and every 15 minutes during 1 hour No
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