AcuGraph and Digestive Symptoms
Can AcuGraph Differentiate Between Participants With and Without Digestive Symptoms
2 other identifiers
observational
30
1 country
1
Brief Summary
This research is designed to study the reliability of the results of an AcuGraph in college students and faculty members with reported digestive symptoms
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Feb 2009
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2009
CompletedFirst Submitted
Initial submission to the registry
February 12, 2009
CompletedFirst Posted
Study publicly available on registry
February 19, 2009
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2010
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2010
CompletedSeptember 15, 2016
September 1, 2016
1.1 years
February 12, 2009
September 14, 2016
Conditions
Outcome Measures
Primary Outcomes (1)
AcuGraph: computerized device to analyze & document the energetic status of the acupuncture meridians
At examination
Secondary Outcomes (1)
IBS Questionnaire
At examination
Study Arms (2)
1 Asymptomatic
students with conditions being studied
2 Symptomatic
students without conditions being studied
Eligibility Criteria
Logan students currently enrolled
You may qualify if:
- 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.
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Logan University, College of Chiropractic
Chesterfield, Missouri, 63017, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Research Associate
Study Record Dates
First Submitted
February 12, 2009
First Posted
February 19, 2009
Study Start
February 1, 2009
Primary Completion
March 1, 2010
Study Completion
March 1, 2010
Last Updated
September 15, 2016
Record last verified: 2016-09