I-THINC: Neuromuscular Cognitive Training

Sponsor
Ke'La H Porter (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05459363
Collaborator
(none)
25
1
9.4

Study Details

Study Description

Brief Summary

This project will utilize a quasi-experimental, multiple baseline pretest-posttest design where participants will complete postural stability assessments, physical performance assessments, and questionnaires to evaluate perceptions toward injury prevention before and after completing a 6-week neuromuscular-cognitive prevention program.

Condition or Disease Intervention/Treatment Phase
  • Other: I-THINC
N/A

Detailed Description

The I-THINC program will address aspects of cognition (i.e., reaction time/processing speed, working memory, cognitive flexibility, inhibitory control, attention, and dual-tasking) while completing common movement patterns utilized in tennis (i.e., lateral shuffle, rapid acceleration/deceleration, and postural stability). The proposed program will take place in the participants training facility. The program will be implemented twice per week for six weeks (12 sessions) with each session lasting 20 minutes. To add variety, there will be two complementary programs (A and B) comprising of four exercises increasing in complexity every two weeks. Each week participants will complete Program A during the first session and Program B during the second session.Exercises will progressively challenge cognitive and physical demand. Exercises were designed to address the most common injuries in tennis.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
25 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Improved Training Happens With Integrated Neuromuscular and Cognitive Challenge
Anticipated Study Start Date :
Aug 1, 2022
Anticipated Primary Completion Date :
May 15, 2023
Anticipated Study Completion Date :
May 15, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Varsity Athletes

Healthy adults recruited from the University of Kentucky varsity tennis programs.

Other: I-THINC
Improved Training Happens with Integrated Neuromuscular and Cognitive Challenge (I-THINC) is an injury prevention program. It will be used to integrate cognitive tasks with traditional sports injury prevention approaches that focus on balance, agility, and neuromuscular control.

Outcome Measures

Primary Outcome Measures

  1. Change in single task static postural stability [6 weeks (baseline, one week after baseline, and immediately following the 6 week intervention)]

    Single task static postural stability will be assessed with an Accusway Plus force plate.

  2. Change in dual task postural stability [6 weeks (baseline, one week after baseline, and immediately following the 6 week intervention)]

    Dual task static postural stability will be assessed with an Accusway Plus force plate while completeing an upper extremity reaction time on the Dynavision D2.

  3. Change in dynamic postural control [6 weeks (baseline, one week after baseline, and immediately following the 6 week intervention)]

    Dynamic postural control will be assessed with the single leg hop.

  4. Change in dual task dynamic postural control [6 weeks (baseline, one week after baseline, and immediately following the 6 week intervention)]

    Dynamic postural control will be assessed with the single leg hop. An additional cognitive task - responding to LED color cues - will be added.

  5. Change in speed, power and agility (single measure) [6 weeks (baseline, one week after baseline, and immediately following the 6 week intervention)]

    Speed, power and agility will be measured using the Run Decide Test.

  6. Change in reactive agility [6 weeks (baseline, one week after baseline, and immediately following the 6 week intervention)]

    Reactive agility will be assessed with the 4x4 box drill.

  7. Change in lower extremity reaction time [6 weeks (baseline, one week after baseline, and immediately following the 6 week intervention)]

    Lower extremity reaction time will be assessed with the lower extremity reaction test, deactivating sensors as quickly as possible with their foot.

  8. Change in HBMS [6 weeks (baseline, one week after baseline, and immediately following the 6 week intervention)]

    Health Belief Model Scale (HBMS) is used to assess behavioral determinants of exercise related injury prevention programs and is comprised of six subscales: susceptibility, severity, benefits, barriers, cues to action, and self-efficacy. Participants rate how strongly they agree or disagree with the statements on a Likert scale ranging from 3 to -3, with a 3 indicating strongly agree and -3 indicating strongly disagree. Positive responses indicate a positive perception towards injury prevention programs, except the barrier subscale where positive responses indicate a negative perception towards injury prevention programs.

  9. Participant engagement [at 6 weeks]

    The participant engagement survey will contain Likert Scale (1-5) questions to provide a quantitative analysis of satisfaction with the program. A 1 indicates strongly disagree and a 5 indicates strongly agree. The range is 7-35, and higher scores indicate increased engagement.

  10. Compliance [6 weeks]

    Compliance will be based on the percentage of sessions attended by participants.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 30 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • healthy adults from the University of Kentucky varsity tennis programs
Exclusion Criteria:
  • not medically cleared for participation

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Ke'La H Porter

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ke'La H Porter, Research Assistant, University of Kentucky
ClinicalTrials.gov Identifier:
NCT05459363
Other Study ID Numbers:
  • 76666
First Posted:
Jul 15, 2022
Last Update Posted:
Jul 15, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Ke'La H Porter, Research Assistant, University of Kentucky
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 15, 2022