Lumbosacral Muscle Sensitivity & Pressure Pain Threshold After Kettlebell Swings

Sponsor
University of Central Florida (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05607212
Collaborator
(none)
90
1
3
13.1
6.9

Study Details

Study Description

Brief Summary

The primary purpose of the study is to assess the muscle contractility and sensitivity of lumbar erector spinae, biceps femoris, and gluteus maximus short-term response to Tabata kettlebell swing protocol.

Condition or Disease Intervention/Treatment Phase
  • Other: Kettlebell Swing
  • Other: Isometric Hold
  • Other: Control
N/A

Detailed Description

While there are many studies that combine resistance exercise with TMG, there are no studies that combine TMG or pressure algometry with an isometric hold of a kettlebell. This will be the first study that will observe the relationship between these specific variable

It has also been noted that kettlebell swings have an acute effect on muscle sensitivity. A study conducted by Hanney et al. (2017) demonstrated that there was an increase in the mean lumbosacral muscle pain pressure threshold across three locations measured.

Research by Hanney et al. is also the only article that has combined kettlebell swings and pressure algometry. As mentioned earlier, these researchers measured the effects of kettlebell swings on pressure pain threshold in the quadratus lumborum, paravertebral muscles, and the piriformis after an acute bout of 2 handed kettle-bell swings. Compared to a control group, the kettlebell swing group had significantly higher pressure pain thresholds for all three of the testing sites.

Researchers believe this may be due to an increased hyperemia-state post exercise, where the increased blood flow and vasodilation flushes out muscle metabolites. Clearing of these metabolites which normally activate chemo-nociceptive free nerve endings, are theorized to decrease pain sensitivity. This post-exercise hyperemia, leading to decreased pressure pain thresholds, may be directly related to the changes in contractility of the muscle after resistive exercise.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
90 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Tensiomyography and Pressure Algometry: Assessing the Effects of an Acute Bout of Kettlebell Swings on Muscle Sensitivity and Pressure Pain Threshold.
Anticipated Study Start Date :
Nov 14, 2022
Anticipated Primary Completion Date :
Nov 14, 2023
Anticipated Study Completion Date :
Dec 18, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Kettlebell Swing Group

Participants will perform two-handed kettlebell swings

Other: Kettlebell Swing
Participants will perform two-handed kettlebell swings using the interval training protocol outlined in the study carried out by Jay et. al. (2011). The protocol calls for 30 seconds of work, followed by 30-60 seconds of rest for a total of 10 intervals. The mechanics of the kettlebell swing will follow those outlined in the study carried out by McGill et. al. (2012). All male participants will perform the intervention with a 16kg kettlebell and all female participants will perform the intervention with a 12kg kettlebell to assure reliability. The weight is higher than previous and similar study by Brandon et al to ensure measurable differences between experimental and comparison groups.

Active Comparator: Active Comparator Group

Participants will perform an isometric hold of a kettlebell for 30 seconds followed by 30 seconds of rest for a total of 10 intervals.

Other: Isometric Hold
Participants will perform an isometric hold of a kettlebell for 30 seconds followed by 30 seconds of rest for a total of 10 intervals. Participants will mimic initial kettlebell swing position by standing shoulder width apart with their back straight, and hips and knees flexed. Participants will be cued to squeeze their glutes and look straight ahead while they hold the weight for the 30 second interval. All male participants will perform the intervention with a 16kg kettlebell and all female participants will perform the intervention with a 12kg kettlebell to assure reliability.

Other: Control group

participants will be educated on the benefit of a kettlebell swing.

Other: Control
Control group: participants will be educated on the benefit of a kettlebell swing.

Outcome Measures

Primary Outcome Measures

  1. Tensiomyography [immediately after the intervention]

    Electrical stimulator (TMG-S1) for lumbar erector spinae, biceps femoris, and gluteus

  2. Pressure Algometry [immediately after the intervention]

    Document pressure change from comfortable pressure to a little unpleasant pain. The measurement will then be collected at the quadratus lumborum, paravertebral muscles, and piriformis.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 35 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Participant is a male or female between the ages of 18 and 35 years old

  • Participant is asymptomatic for low back pain

Exclusion Criteria:
  • Participant is unable to participate in physical activity, as determined by the PAR-Q+

  • Have any injuries or other chronic pain that would prevent them from performing a high intensity kettlebell swing protocol

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Central Florida Orlando Florida United States 32816

Sponsors and Collaborators

  • University of Central Florida

Investigators

  • Principal Investigator: William J. Hanney, University of Central Florida

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Central Florida
ClinicalTrials.gov Identifier:
NCT05607212
Other Study ID Numbers:
  • STUDY00004622
First Posted:
Nov 7, 2022
Last Update Posted:
Nov 7, 2022
Last Verified:
Oct 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 University of Central Florida
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 7, 2022