Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
114 participants
INTERVENTIONAL
2020-11-19
2024-03-19
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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Intervention Group
Subjects will participate in a 15 minute postural intervention program 2-3 times per week
Postural Intervention Program
Dynamic warmup program designed to target several areas of physical and mental wellbeing.
Control Group
Subjects will NOT participate in any postural intervention.
No interventions assigned to this group
Interventions
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Postural Intervention Program
Dynamic warmup program designed to target several areas of physical and mental wellbeing.
Eligibility Criteria
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Inclusion Criteria
* Participants also must have a normal (18.5-24.9kg/m2) or overweight BMI (25-29.9kg/m2).
* Participants must be able to speak, listen, read, and understand sentences written in English.
Exclusion Criteria
* History of falls, osteoporosis, osteoarthritis, or orthopedic or neurological conditions (i.e., stroke)
* Medications that cause dizziness or slow movement
* Smoke
* Body mass to height squared ratio greater than 30kg/m2 or less than 18.4kg/m2, blood pressure greater than 140/90 mmHg, or a history of heart conditions.
* Individuals with progressive cognitive, neurologic disorders, cancer treatment, chronic heart failure, or unstable medical conditions
12 Years
ALL
Yes
Sponsors
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Mayo Clinic
OTHER
Responsible Party
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Benjamin (Ben) D. Holmes
Principal Investigator
Principal Investigators
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Benjamin Holmes, DC, PhD
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Locations
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Mayo Clinic in Rochester
Rochester, Minnesota, United States
Countries
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Related Links
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Mayo Clinic Clinical Trials
Other Identifiers
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20-004586
Identifier Type: -
Identifier Source: org_study_id
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