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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00163124
Other study ID # PCC2005-003
Secondary ID
Status Completed
Phase N/A
First received September 9, 2005
Last updated September 12, 2005
Start date March 2005
Est. completion date August 2005

Study information

Verified date September 2005
Source Parker College of Chiropractic
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

There are a variety of treatment approaches used by the chiropractic profession. Some of these require forceful joint manipulation and some do not. This study is designed to compare outcomes of two such techniques that are common to chiropractic practice. The hypothesis is that there is no difference between forceful and non-forceful approaches to treatment.


Description:

The comparison will permit a one month treatment period for both techniques and a three week follow-up. Patients will be assessed at baseline (intake), and at specified intervals and at three weeks following the termination of care.


Recruitment information / eligibility

Status Completed
Enrollment 155
Est. completion date August 2005
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

chronic musculoskeletal pain ability to communicate in English

Exclusion Criteria:

pregnancy contraindications to manipulation pending litigation chiropractic care within the last month

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Single Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
spinal manipulation & patient education/nutrition


Locations

Country Name City State
United States Parker College of Chiropractic Dallas Texas

Sponsors (1)

Lead Sponsor Collaborator
Parker College of Chiropractic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain Disability Index (PDI)
Secondary Beck Depression Inventory
Secondary Patient Expectation
Secondary Evaluation of Clinic Services
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