Acute Effect of Motor-Cognitive Training

K

Ke'La H Porter

Status

Completed

Conditions

Injury;Sports

Treatments

Other: Motor-Cognitive Training Program

Study type

Interventional

Funder types

Other

Identifiers

NCT06017154
88851

Details and patient eligibility

About

Participants will complete a functional MRI to evaluate brain activation, functional connectivity, and behavioral performance immediately before and after a training program (approximately 30 minutes). The training program will comprise of integrate neuromuscular (agility, dynamic postural stability, shuffling, rapid acceleration/deceleration, plyometrics, lateral shuffle, and core stability) and cognitive (reaction time, processing speed, task switching, decision-making, and working memory) challenges.

Enrollment

21 patients

Sex

Female

Ages

18 to 25 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Physically active

Exclusion criteria

  • Injury to the muscle or bone (upper extremity, lower extremity, or back) within the past 3 months
  • Had musculoskeletal surgery or fracture (required open reduction internal fixation or within the last 12 months)
  • Had a concussion or mild head injury within the last year
  • Have been diagnosed with any kind of neurological, vestibular, or visual disturbance that impairs mobility
  • Currently taking medications that affect the central nervous system
  • Pregnant or suspicions of being pregnant
  • Have metal fragments, pins, plates, or clips, shrapnel, body piercings that cannot be removed, have surgical implants or orthodontics that cannot be removed
  • Have claustrophobia
  • Have a history of cognitive impairment

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

21 participants in 1 patient group

Physically active females
Experimental group
Description:
Healthy active females between 18 and 25
Treatment:
Other: Motor-Cognitive Training Program

Trial contacts and locations

1

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Central trial contact

Ke'La H Porter, MS; Matthew C Hoch, PhD

Data sourced from clinicaltrials.gov

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