- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00740350
Logan Basic During Pregnancy on Labor and Childbirth
August 22, 2008 updated by: Logan College of Chiropractic
Does the Logan Basic Protocol for Chiropractic Care During Pregnancy Reduce Labor Time and Increase the Ease of Labor and Childbirth?
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.
Study Overview
Detailed 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.
Study Type
Interventional
Enrollment (Anticipated)
50
Phase
- Phase 2
- Phase 1
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Missouri
-
Chesterfield, Missouri, United States, 63017
- Recruiting
- Logan University, College of Chiropractic
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
14 years to 46 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental
Logan Basic chiropractic adjustments during pregnancy.
|
Logan Basic chiropractic adjustments during pregnancy.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Post delivery interview/questionnaire
Time Frame: 2 weeks post delivery
|
2 weeks post delivery
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2007
Primary Completion (Anticipated)
February 1, 2009
Study Completion (Anticipated)
February 1, 2009
Study Registration Dates
First Submitted
August 21, 2008
First Submitted That Met QC Criteria
August 22, 2008
First Posted (Estimate)
August 25, 2008
Study Record Updates
Last Update Posted (Estimate)
August 25, 2008
Last Update Submitted That Met QC Criteria
August 22, 2008
Last Verified
August 1, 2008
More Information
Terms related to this study
Other Study ID Numbers
- SR0627080139
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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