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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT01123226
Other study ID # AECC05052010
Secondary ID
Status Not yet recruiting
Phase Phase 2
First received May 13, 2010
Last updated May 13, 2010
Start date September 2010
Est. completion date June 2011

Study information

Verified date May 2010
Source Anglo-European College of Chiropractic
Contact Hugh A Gemmell, DC, EdD
Phone 44 1202436200
Email hgemmell@aecc.ac.uk
Is FDA regulated No
Health authority United Kingdom: Research Ethics Committee
Study type Interventional

Clinical Trial Summary

There will be no difference between trigger point therapy and spinal manipulation in correcting a spine joint dysfunction in the back


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 60
Est. completion date June 2011
Est. primary completion date June 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 64 Years
Eligibility Inclusion Criteria:

- mechanical thoracic back pain

- age 18-64

- presence of at least one spinal manipulable lesion

- presence of a trigger point associated with the spinal manipulable lesion

- able to lie prone on a treatment table for 15 minutes

Exclusion Criteria:

- absolute contraindications to spinal manipulation

- specific thoracic back pain

- bleeding diathesis, use of anticoagulants, long-term corticosteroid use

- involved in litigation for thoracic back pain

- inability to read or write English fluently

- treatment with manipulation or myofascial therapy within past three days

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
spinal manipulation
A maximum of two high velocity low amplitude spinal manipulations to one dysfunctional spine joint
trigger point therapy
The thumb will apply firm pressure to a trigger point in the paravertebral multifidus and rotatores muscles associated with the spine joint dysfunction using the barrier approach. This will be held until the barrier releases and this will continue until the trigger point is inactivated or 3 minutes has passed.

Locations

Country Name City State
United Kingdom Anglo-European College of Chiropractic Bournemouth Dorset

Sponsors (1)

Lead Sponsor Collaborator
Anglo-European College of Chiropractic

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Correction of spinal manipulable lesion Dichotomous data either lesion is corrected or not. Immediate effect of one treatment No
Secondary Change in pressure pain threshold over the involved spinous process The point at which sensation changes from that of pressure to pain is measured in Kg/cm2 Immediate effect of one treatment No
See also
  Status Clinical Trial Phase
Completed NCT03892759 - Osteopathic Manipulative Treatment for Back Pain N/A