NCT04204460

Brief Summary

Previous studies have generally investigated patellar tendon stiffness, cross-sectional area of patellar tendon, patellar tendon length, patellar force and patellafemoral forces during decline squat. However, there is just a few study about electromyographic (EMG) activity during the eccentric squating, which is about rectus femoris (RF) recruitment. In the present study the investigators primarly aimed to quantify the activation of RF, vastus lateralis (VL), and vastus medialis obliqus (VMO) during eccentric squat on different decline angle (0, 5°, 10°, 15°, 20°). An additional purpose of our study was to compare the changes in muscle activation at various arc of knee flexion motion (degrees of 0-30, 30-60, 60-90, 0-60, 30-90, 0-90).The investigators hypothesised that the recruitment of RF, VL, and VMO during eccentric squat would differ according to decline angle and arc of motion.

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
20

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Dec 2019

Geographic Reach
1 country

1 active site

Status
unknown

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

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 6, 2019

Completed
9 days until next milestone

Study Start

First participant enrolled

December 15, 2019

Completed
4 days until next milestone

First Posted

Study publicly available on registry

December 19, 2019

Completed
2 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 21, 2019

Completed
1 day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 22, 2019

Completed
Last Updated

December 19, 2019

Status Verified

December 1, 2019

Enrollment Period

6 days

First QC Date

December 6, 2019

Last Update Submit

December 16, 2019

Conditions

Keywords

eccentric squattingelectromyografic activationexercisepatellar tendinopathy

Outcome Measures

Primary Outcomes (3)

  • Electromyographic measurement of muscle activation

    Surface electromyographic (EMG) system (Noraxon Telemyo DTS System, Scottsdale, USA) will be use to measure the muscle activation ratios of RF, VL, and VMO. Electrodes will be placed according to Surface EMG for noninvasive assessment of muscles (SENIAM) recommendations on the dominant leg. The muscle activation during eccentric phase of the decline squat for RF, VL, and VMO will be determined. The decline squat will be performed under different conditions (various decline angle: 0, 5, 10,15, 20 degree) The muscle activation will also be investigated within various arc of motion of knee flexion (0-30, 30-60, 60-90, 0-60, 0-90, 30-90) which is determined using the motion analysis system (Noraxon, MYOmotion Scottsdale, USA).

    50 minutes

  • Maximal voluntary isometric contractions (MVICs)

    MVICs for the RF, VL, and VMO at their manual muscle test positions will be assessed within 3 trials, which lasts 5 seconds. The muscle test position will be standardized 90 degrees hip flexion and 60 degrees knee flexion. One minute a rest period will be between each trial. The peak EMG amplitude will be used for the normalization.

    5 minutes

  • Normalized EMG values

    The amount of muscle activation in each condition will be proportioned to MVICs value for normalization using a calculator. The value will be represented in percentile (%).

    5 minutes

Secondary Outcomes (2)

  • Weight

    1 minute

  • Height

    1 minute

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Asymptomathic older than 18 years, voluntary subjects who are students in a high school of physical education and sports.

You may qualify if:

  • had exercised regularly (\>3 days in a week) for at least six months.
  • older than 18 years old.

You may not qualify if:

  • had patellofemoral pain, knee pain otherwise unrelated to the knee extensor mechanism and other injuries that would restrict performance of the tasks (e.g. ankle pathology).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Sevim ACARÖZ CANDAN

Ordu, Altinordu, 52100, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Motor Activity

Condition Hierarchy (Ancestors)

Behavior

Study Officials

  • Sevim Acaröz Candan, PhD

    Ordu University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Sevim Acaröz Candan, PhD

CONTACT

Study Design

Study Type
observational
Observational Model
CASE CROSSOVER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Head of Department of Physiotherapy and Rehabilitation

Study Record Dates

First Submitted

December 6, 2019

First Posted

December 19, 2019

Study Start

December 15, 2019

Primary Completion

December 21, 2019

Study Completion

December 22, 2019

Last Updated

December 19, 2019

Record last verified: 2019-12

Data Sharing

IPD Sharing
Will not share

Locations