Acute Responses of Postural Alignment, Kinematic Synergy, and Intermuscular Coherence to Postural Muscle Facilitation

Sponsor
Radford University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05608850
Collaborator
(none)
15
1
2
6.2
2.4

Study Details

Study Description

Brief Summary

Clinicians frequently assess and intervene on postural alignment. However, research demonstrating the effects of exercise interventions in moving postural alignment toward an evidence-based standard is lacking. Part of the difficulty in establishing such evidence has been a lack of theory-motivated conceptions of what "good" posture is. In other words, the prevailing understanding of postural alignment is based on the negation of what has been observed to associate with bad outcomes. This study will build upon preliminary findings from our laboratory that define good postural alignment on theoretical grounds. The investigators will measure motion capture and muscle activation patterns during simple postural alignment tasks before and after 1) a corrective exercise intervention, or 2) a control intervention based designed to inhibit superficial muscle tension. The corrective exercise intervention is designed to counteract the natural patterns in which the human skeleton tends to collapse from a standing position under the influence of gravity. The control intervention consists of passive, partner-assisted stretching. Regardless of initial assignment, all participants will crossover (i.e. switch interventions) and repeat the study procedures after a 1-week washout period. Behavioral indicators of movement and nervous system coordination will be used to quantify alignment before and after exercise, as well as the consistency of those alignment patterns with theoretically-defined standards. The knowledge gained from this study will contribute to evidence-based definitions of healthy postural alignment and help identify effective interventions by which clinicians can promote good posture.

Condition or Disease Intervention/Treatment Phase
  • Other: Exercise Then Stretch
  • Other: Stretch Then Exercise
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
15 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Acute Responses of Postural Alignment, Kinematic Synergy, and Intermuscular Coherence to Postural Muscle Facilitation
Actual Study Start Date :
Oct 25, 2022
Anticipated Primary Completion Date :
May 1, 2023
Anticipated Study Completion Date :
May 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Other: Exercise Then Stretch

Participants in AB will perform the experimental (exercise) intervention first and the control (stretch) intervention second

Other: Exercise Then Stretch
This arm (sequence) will perform an anti-gravity kinetic chain intervention and then a passive, partner-assisted stretching intervention, separated by a one-week washout period.

Other: Stretch Then Exercise
This arm (sequence) will perform a passive, partner-assisted stretching intervention and then an anti-gravity kinetic chain intervention , separated by a one-week washout period.

Other: Stretch Then Exercise

Participants in BA will perform the experimental (exercise) intervention second and the control (stretch) intervention first

Other: Exercise Then Stretch
This arm (sequence) will perform an anti-gravity kinetic chain intervention and then a passive, partner-assisted stretching intervention, separated by a one-week washout period.

Other: Stretch Then Exercise
This arm (sequence) will perform a passive, partner-assisted stretching intervention and then an anti-gravity kinetic chain intervention , separated by a one-week washout period.

Outcome Measures

Primary Outcome Measures

  1. Euclidean distance from the vector describing subject-specific, simulated gravitational collapse [Immediately before Intervention (Day 1)]

    This outcome is a cumulative descriptor of segment angle distance from the pattern in which an individual's posture would collapse. The reference point for each individual is calculated using both pre and post-intervention data for a given day.

  2. Euclidean distance from the vector describing subject-specific, simulated gravitational collapse [Immediately after Intervention (Day 1)]

    This outcome is a cumulative descriptor of segment angle distance from the pattern in which an individual's posture would collapse. The reference point for each individual is calculated using both pre and post-intervention data for a given day.

  3. Euclidean distance from the vector describing subject-specific, simulated gravitational collapse [Immediately before Intervention (Day 7)]

    This outcome is a cumulative descriptor of segment angle distance from the pattern in which an individual's posture would collapse. The reference point for each individual is calculated using both pre and post-intervention data for a given day.

  4. Euclidean distance from the vector describing subject-specific, simulated gravitational collapse [Immediately after Intervention (Day 7)]

    This outcome is a cumulative descriptor of segment angle distance from the pattern in which an individual's posture would collapse. The reference point for each individual is calculated using both pre and post-intervention data for a given day.

  5. Pooled intermuscular coherence [Immediately before Intervention (Day 1)]

    Weighted average of frequency-domain correlations between muscle pairs belonging to anterior, posterior, and trunk muscle groups.

  6. Pooled intermuscular coherence [Immediately after Intervention (Day 1)]

    Weighted average of frequency-domain correlations between muscle pairs belonging to anterior, posterior, and trunk muscle groups.

  7. Pooled intermuscular coherence [Immediately before Intervention (Day 7)]

    Weighted average of frequency-domain correlations between muscle pairs belonging to anterior, posterior, and trunk muscle groups.

  8. Pooled intermuscular coherence [Immediately after Intervention (Day 7)]

    Weighted average of frequency-domain correlations between muscle pairs belonging to anterior, posterior, and trunk muscle groups.

Secondary Outcome Measures

  1. Top-down kinetic chain continuity [Immediately before Intervention (Day 1)]

    The purpose of this outcome is to quantify the communication of motion from the upper body to the lower body. In a test involving placing hands-on-head and pulling the elbows back as far as possible, the response in the lower body is quantified by posterior rotation of the tibial segment.

  2. Top-down kinetic chain continuity [Immediately after Intervention (Day 1)]

    The purpose of this outcome is to quantify the communication of motion from the upper body to the lower body. In a test involving placing hands-on-head and pulling the elbows back as far as possible, the response in the lower body is quantified by posterior rotation of the tibial segment.

  3. Top-down kinetic chain continuity [Immediately before Intervention (Day 7)]

    The purpose of this outcome is to quantify the communication of motion from the upper body to the lower body. In a test involving placing hands-on-head and pulling the elbows back as far as possible, the response in the lower body is quantified by posterior rotation of the tibial segment.

  4. Top-down kinetic chain continuity [Immediately after Intervention (Day 7)]

    The purpose of this outcome is to quantify the communication of motion from the upper body to the lower body. In a test involving placing hands-on-head and pulling the elbows back as far as possible, the response in the lower body is quantified by posterior rotation of the tibial segment.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 40 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Healthy adult

  • 18 - 40 years of age

Exclusion Criteria:
  • Recent (< 6 months) history of lower extremity injury

  • Recent (< 6 months) history of other musculoskeletal or neurological disorder affecting balance

  • Contraindications to participation in physical activity

Contacts and Locations

Locations

Site City State Country Postal Code
1 Radford University Carilion Roanoke Virginia United States 24013

Sponsors and Collaborators

  • Radford University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Stephen Glass, Assistant Professor, Radford University
ClinicalTrials.gov Identifier:
NCT05608850
Other Study ID Numbers:
  • 2021-288-RUC
First Posted:
Nov 8, 2022
Last Update Posted:
Nov 8, 2022
Last Verified:
Nov 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Stephen Glass, Assistant Professor, Radford University

Study Results

No Results Posted as of Nov 8, 2022