NCT06069271

Brief Summary

The purpose of this randomized control trial is to determine the extent of muscle fatigue in the lumbar erector spinae musculature secondary to a high-intensity interval kettlebell swing protocol utilizing TMG previously published by Jay et. al in 2011.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
41

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Mar 2020

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 4, 2020

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 8, 2022

Completed
10 months until next milestone

Study Completion

Last participant's last visit for all outcomes

January 15, 2023

Completed
8 months until next milestone

First Submitted

Initial submission to the registry

September 25, 2023

Completed
10 days until next milestone

First Posted

Study publicly available on registry

October 5, 2023

Completed
Last Updated

October 5, 2023

Status Verified

September 1, 2023

Enrollment Period

2 years

First QC Date

September 25, 2023

Last Update Submit

September 29, 2023

Conditions

Outcome Measures

Primary Outcomes (1)

  • Tensiomyography

    Research has progressed to support the test-retest and inter-rater reliability using TMG for measurement of muscle contraction. TMG demonstrates good to excellent relative reliability(0.80-0.99) and inter-rater ICC between 0.77-0.97 Across all five TMG parameters.4-7

    Baseline, immediate after exercise, 24 hours after exercise

Study Arms (2)

Rest

NO INTERVENTION

Subjects in the control group were instructed to complete the general warm up followed by a 10-minute rest period.

Exercise

EXPERIMENTAL

The intervention group completed two-handed Russian KBSs using an interval training protocol outlined by Jay et al.10 involving 30 seconds of work followed by 30 seconds of rest for 10 total intervals. Prior to completing the intervention, participants completed a general warmup consisting of 10 non-weighted squats, 10 non-weighted dead-lifts, and 10 dowel rod shoulder flexion repetitions. Participants were instructed to perform all warm-up activities at an intensity of 70% of maximal effort using a Rate of Perceived Exertion scale(RPE).

Other: Kettlebell swing

Interventions

The intervention group completed two-handed Russian KBSs using an interval training protocol outlined by Jay et al.10 involving 30 seconds of work followed by 30 seconds of rest for 10 total intervals. Prior to completing the intervention, participants completed a general warmup consisting of 10 non-weighted squats, 10 non-weighted dead-lifts, and 10 dowel rod shoulder flexion repetitions. Participants were instructed to perform all warm-up activities at an intensity of 70% of maximal effort using a Rate of Perceived Exertion scale(RPE).

Exercise

Eligibility Criteria

Age18 Years - 45 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Ages of 18 and 45 years of age.
  • Clear PAR-Q

You may not qualify if:

  • history of low back pain
  • pre-existing injuries
  • If "YES" was the response to any of the seven questions in the PAR-Q, the participant was deemed to be unable to exercise safely.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Central Florida

Orlando, Florida, 32816, United States

Location

Related Publications (1)

  • Hanney WJ, Perez A, Collado G, Palmer AC, Wilson AT, Richardson RM, Kolber MJ. The Immediate Effects of a Standardized Kettlebell Swing Protocol on Lumbar Paraspinal Muscle Function: A Randomized Controlled Trial. J Strength Cond Res. 2024 Nov 1;38(11):1854-1859. doi: 10.1519/JSC.0000000000004892. Epub 2024 Aug 14.

Study Officials

  • William J Hanney, PhD

    University of Central Florida

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
Assessor was blinded to group assignment
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Randomized Control Trial
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Clinical Assistant Professor

Study Record Dates

First Submitted

September 25, 2023

First Posted

October 5, 2023

Study Start

March 4, 2020

Primary Completion

March 8, 2022

Study Completion

January 15, 2023

Last Updated

October 5, 2023

Record last verified: 2023-09

Data Sharing

IPD Sharing
Will not share

Locations