- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02749266
The Impact of Chiropractic Activator Adjustments on Mental Rotation and Line Judgment Reaction Time
The Impact of Chiropractic Activator Adjustments on Mental Rotation and Line Judgment Reaction Time: A Pilot Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This study seeks to assess the impact of chiropractic on cognition. Participants must be between 18 and 35 years of age. Within the past six months individuals may not participate if they have had any broken bones, accidents, or surgeries to their spine. Additionally, participants cannot have any mental disabilities, be pregnant, or have other conditions of the spine such as bone mineral loss.
Patients will receive a chiropractic exam and will be randomized to a sham (simulated chiropractic adjustment) or chiropractic adjustment intervention group. Prior to receiving either the sham or chiropractic adjustment, the participants will sit in front of a computer screen and will be asked to follow instructions and press a button on a keypad. There will be three different types of computer assessments that will take approximately fifteen minutes total. After the computer assessments the participant will receive either the sham or chiropractic adjustment. The chiropractic adjustment and the sham will both utilize a handheld instrument called an Activator. After the adjustment or sham the participant will take the computer assessments again. The total time this may take is ninety minutes.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Georgia
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Marietta, Georgia, United States, 30060
- Life University
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Age 18 to 35
- In good health
Exclusion Criteria:
- pregnant
- medically diagnosed cognitive deficits
- medically diagnosed learning disabilities
- fractures, traumas, or surgeries to the spine within the past six months
- diagnosed osteoporosis, articular instability
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Chiropractic Activator Adjustment
Participant will receive a chiropractic adjustment utilizing a handheld chiropractic instrument called an Activator.
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Participant will receive a chiropractic adjustment utilizing a handheld chiropractic instrument called an Activator.
Other Names:
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Sham Comparator: Chiropractic sham adjustment
Participant will receive a sham (simulated) chiropractic adjustment utilizing a handheld chiropractic instrument called an Activator.
|
Participants will receive a simulated chiropractic adjustment with a handheld adjusting instrument called an Activator.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Reaction time
Time Frame: Pre and Post intervention (average of 90 minutes)
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Reaction time assessment of keyboard responses to computerized stimulus presentations
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Pre and Post intervention (average of 90 minutes)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Response correctness
Time Frame: Pre and post intervention (average of 90 minutes)
|
Correct response to computerized stimulus presentations
|
Pre and post intervention (average of 90 minutes)
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Stephanie Sullivan, D.C., Life University
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- I-0011
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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