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NCT00740350 Clinical Trial

Logan Basic During Pregnancy on Labor and Childbirth

Pregnancy Clinical Trial

Official title:
Does the Logan Basic Protocol for Chiropractic Care During Pregnancy Reduce Labor Time and Increase the Ease of Labor and Childbirth?

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT00740350
Other study ID # SR0627080139
Secondary ID
Status Recruiting
Phase Phase 1/Phase 2
First received August 21, 2008
Last updated August 22, 2008
Start date March 2007
Est. completion date February 2009

Study information
Verified date August 2008
Source Logan College of Chiropractic
Contact Patrick Montgomery, DC
Phone 636-230-2100
Email patrick.montgomery@logan.edu
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine if women who have chiropractic care, according to the Logan Basic Protocol for adjusting, during pregnancy have an easier, shorter labor and delivery as compared to women who haven't had chiropractic care during pregnancy.

Description:

This study will be designed to test if the Logan Basic Technique system of adjusting pregnant women can reduce labor time and increase the ease of labor and delivery as compared to the labor times reported by Kilpatrick and Laros in the obstetric literature. It is proposed that women who have regular chiropractic care throughout pregnancy or at least for the third trimester will have an easier labor and delivery as well as a shorter labor time than is reported in the literature.

Recruitment information / eligibility
Status Recruiting
Enrollment 50
Est. completion date February 2009
Est. primary completion date February 2009
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- 20-24 weeks pregnant

- enrolled in a separate pre-natal care protocol with an outside provider

- a Logan College Student or member of the family of a Logan Student ("family" as defined by CCE designation)

Exclusion Criteria:

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Intervention

Procedure:
• Logan Basic
Logan Basic chiropractic adjustments during pregnancy.

Locations
Country Name City State
United States Logan University, College of Chiropractic Chesterfield Missouri

Sponsors (1)
Lead Sponsor Collaborator
Logan College of Chiropractic

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Post delivery interview/questionnaire 2 weeks post delivery No
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