Acute Effects of Dynamic Stretching, Plyometrics, and Loading on Achilles Tendon Properties and Performance Outcomes

December 4, 2023 updated by: Matt Dewald, University of South Dakota
The study will be looking at acute changes in Achilles tendon properties and changes in a vertical single leg hop following an exercise intervention. The three exercise interventions will be randomized and take place on separate days 1 week apart. The three exercise interventions are AAROM, slow load, and plyometrics.

Study Overview

Status

Completed

Conditions

Detailed Description

The purpose of the study is to determine if there are acute changes in Achilles tendon properties and changes in performance based on what tendon exercise intervention is being used. About 70 people will take part in this research.

Study Type

Interventional

Enrollment (Actual)

5

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • South Dakota
      • Vermillion, South Dakota, United States, 57069
        • Sanford Coyote Sport Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

14 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • College student

Exclusion Criteria:

  • Unable to complete interventions

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Group 1
Randomized AAROM, Slow Load, or Plyometric intervention
AAROM with knee to wall exercise, 3x30 reps
Single leg heel raise, 3x10 reps
Double leg 5 inch wall hops, 3x10 sec
Experimental: Group 2
Randomized AAROM, Slow Load, or Plyometric intervention
AAROM with knee to wall exercise, 3x30 reps
Single leg heel raise, 3x10 reps
Double leg 5 inch wall hops, 3x10 sec
Experimental: Group 3
Randomized AAROM, Slow Load, or Plyometric intervention
AAROM with knee to wall exercise, 3x30 reps
Single leg heel raise, 3x10 reps
Double leg 5 inch wall hops, 3x10 sec

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Achilles Tendon Stiffness
Time Frame: immediately
A myotonometer will measure the stiffness in N/m.
immediately
Achilles Tendon Natural Oscillation
Time Frame: immediately
A myotonometer will measure the natural oscillation frequency in Hz.
immediately
Achilles Tendon Logarithmic Decrement
Time Frame: immediately
A myotonometer will measure logarithmic decrement, which is a measure of elasticity.
immediately
Achilles Tendon Mechanical Stress Relaxation Time
Time Frame: immediately
A myotonometer will measure mechanical stress relaxation time in ms.
immediately
Achilles Tendon Creep
Time Frame: immediately
A myotonometer will measure creep in De.
immediately

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Single-leg drop jump vertical
Time Frame: immediately
Single-leg vertical drop jump from 4-inch box with knee locked in extension will be measured in cm. A higher jump is considered better.
immediately
Reactive Strength Index
Time Frame: immediately
Reactive Strength Index will be measured as an AU, the higher the better.
immediately
Flight Time
Time Frame: immediately
Flight time will be measured in ms, the higher the better.
immediately
Contact Time
Time Frame: immediately
Contact time will be measured in ms, the lower the better.
immediately
Limb Stiffness
Time Frame: immediately
Limb stiffness will be measured in kN/m, generally the higher the better.
immediately

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 18, 2023

Primary Completion (Actual)

October 3, 2023

Study Completion (Actual)

October 3, 2023

Study Registration Dates

First Submitted

September 1, 2022

First Submitted That Met QC Criteria

September 1, 2022

First Posted (Actual)

September 6, 2022

Study Record Updates

Last Update Posted (Estimated)

December 11, 2023

Last Update Submitted That Met QC Criteria

December 4, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 22-211

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

Data will be available upon request

IPD Sharing Time Frame

If required with the publication, a link to de-identified data will be provided.

IPD Sharing Access Criteria

IPD will be available upon request

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • ANALYTIC_CODE
  • CSR

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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