- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00846794
AcuGraph and Digestive Symptoms
September 14, 2016 updated by: Brian Snyder, DC, Logan College of Chiropractic
Can AcuGraph Differentiate Between Participants With and Without Digestive Symptoms
This research is designed to study the reliability of the results of an AcuGraph in college students and faculty members with reported digestive symptoms
Study Overview
Status
Completed
Detailed Description
The specific aim of the study is to test the reliability of the AcuGraph in subjects with irritable bowel syndrome (IBS).
The hypothesis is that the AcuGraph will be a reliable method to identify disorders in subjects.
Study Type
Observational
Enrollment (Actual)
30
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
-
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Missouri
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Chesterfield, Missouri, United States, 63017
- 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
18 years to 65 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Logan students currently enrolled
Description
Inclusion Criteria:
- Subjects will be required to answer a questionnaire evaluating for a percentage of digestive disorders "disability" based on the subject's answers. If a participant's answers do not qualify as a disability, they will be assigned to the asymptomatic group and will still be examined with an AcuGraph to provide normative data.
Exclusion Criteria:
- heart condition
- kidney disorder
- thyroid disorders
- diabetes
- chronic disease or illness
- neurological diseases
- skin or bleeding disorders
- pregnant
- currently taking drugs or nutritional supplements
- pacemaker and/or
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
Cohorts and Interventions
Group / Cohort |
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1 Asymptomatic
students with conditions being studied
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2 Symptomatic
students without conditions being studied
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
AcuGraph: computerized device to analyze & document the energetic status of the acupuncture meridians
Time Frame: At examination
|
At examination
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
IBS Questionnaire
Time Frame: At examination
|
At examination
|
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
February 1, 2009
Primary Completion (ACTUAL)
March 1, 2010
Study Completion (ACTUAL)
March 1, 2010
Study Registration Dates
First Submitted
February 12, 2009
First Submitted That Met QC Criteria
February 17, 2009
First Posted (ESTIMATE)
February 19, 2009
Study Record Updates
Last Update Posted (ESTIMATE)
September 15, 2016
Last Update Submitted That Met QC Criteria
September 14, 2016
Last Verified
September 1, 2016
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SR1219080169
- 400
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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