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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RECRUITING
NA
40 participants
INTERVENTIONAL
2025-10-27
2028-10-27
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
PREVENTION
TRIPLE
Study Groups
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Isometric Handgrip Training - Intervention
Participants will perform moderate-intensity handgrip training three days per week for eight weeks using a handheld device.
Handgrip Training
Handgrip training 3 days per week for 8 weeks
Isometric Handgrip Training - Sham
Participants will perform very low-intensity handgrip training three days per week for eight weeks using a handheld device.
Handgrip Training
Handgrip training 3 days per week for 8 weeks
Interventions
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Handgrip Training
Handgrip training 3 days per week for 8 weeks
Eligibility Criteria
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Inclusion Criteria
* Body mass index ≤30 kg/m2 (without obesity)
* Physically inactive (not meeting the current recommendations of ≥150 minutes per week of moderate-to-vigorous aerobic exercise and not ≥2 days per week of resistance training) in last 6 months
* Have a smartphone and are willing to download mobile applications used in this project
Exclusion Criteria
* Being pregnant, planning to become pregnant, or breastfeeding/lactating
* Regular use of nicotine products in the past 6 months
* Recent head injury/trauma or concussion
18 Years
35 Years
ALL
Yes
Sponsors
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Florida State University
OTHER
Responsible Party
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Joseph Watso
Laboratory Director
Locations
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Florida State University
Tallahassee, Florida, United States
Countries
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Facility Contacts
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Other Identifiers
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STUDY00006271
Identifier Type: -
Identifier Source: org_study_id
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