The Influence of Running and Velocity to Kinematic Parameters

January 3, 2017 updated by: Yu Zhang, Guangzhou General Hospital of Guangzhou Military Command
Some researches have found that gait posture velocity have influence on kinematic parameters. However, how the gait velocity and posture will influence kinematic parameters remain unclear. In addition to walking, running is one of the most daily activities of people. The purpose of this research is to find out the influence of gait velocity and running to kinematic parameters . To do this, it will provide a reference for future prospective studies or investigations and make us fully understand the impact of gait velocity and running to kinematic parameters of gait.

Study Overview

Status

Status

Indicates the current recruitment status or the expanded access status.
Unknown

Conditions

Conditions

The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.

Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.

Study Type

Study Type

Describes the nature of a clinical study. Study types include interventional studies (also called clinical trials), observational studies (including patient registries), and expanded access.
Observational

Enrollment (Anticipated)

Enrollment

The number of participants in a clinical study. The "anticipated" enrollment is the target number of participants that the researchers need for the study.
30

Contacts and Locations

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

Study Contact

Study Contact

The name and contact information for the person who can answer enrollment questions for a clinical study. Each location where the study is being conducted may also have a specific contact, who may be better able to answer those questions.
  • Name: Yu Zhang, PhD
  • Phone Number: +86-20-88654440

Study Contact Backup

  • Name: Limin Ma, PhD

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

Eligibility Criteria

The key requirements that people who want to participate in a clinical study must meet or the characteristics they must have. Eligibility criteria consist of both inclusion criteria (which are required for a person to participate in the study) and exclusion criteria (which prevent a person from participating). Types of eligibility criteria include whether a study accepts healthy volunteers, has age or age group requirements, or is limited by sex.

Ages Eligible for Study

20 years to 30 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

All the participants will be recruited via university advertisement.

Description

Inclusion Criteria:

i) 20< age < 30. ii) Body mass index < 30. iii) No history of major injury or surgery in lower limbs. iv) No symptoms of lower limbs. v) Physical examination to test the lower limbs to be normal. vi) The habit of moderate exercise (e.g. Jogging )at least once a week for at least 30 minutes

Exclusion Criteria:

i)Body mass index >30. ii) Injury or surgery in hip/knee/ankle. iii) History trauma in the lower limbs (e.g. fracture). iv) Neuropathic disease . v) Muscular disease. vi) Lack ability to finish the procedure physically or mentally. vii) Easy to fall. viii) Any other conditions that can influence gait parameters of the lower limbs.

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

Cohorts and Interventions

Group / Cohort

Group / Cohort

A group or subgroup of participants in an observational study that is assessed for biomedical or health outcomes.
Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.
WV 1
The condition of this group will be set as participants walking at 3.5km/h
Procedure: Walk and Run
Once participants are eligible, they will undergo the experimental procedure. Before data collection, they will walk or run on a treadmill in barefoot for ten minutes to adapt the condition. The a gait analysis system will collect the data while they walk or run on the treadmill in barefoot at selected gait speed.
WV 2
The condition of this group will be set as participants walking at 4.0km/h
Procedure: Walk and Run
Once participants are eligible, they will undergo the experimental procedure. Before data collection, they will walk or run on a treadmill in barefoot for ten minutes to adapt the condition. The a gait analysis system will collect the data while they walk or run on the treadmill in barefoot at selected gait speed.
RV 1
The condition of this group will be set as participants running at 3.5km/h
Procedure: Walk and Run
Once participants are eligible, they will undergo the experimental procedure. Before data collection, they will walk or run on a treadmill in barefoot for ten minutes to adapt the condition. The a gait analysis system will collect the data while they walk or run on the treadmill in barefoot at selected gait speed.
RV 2
The condition of this group will be set as participants running at 4.0km/h
Procedure: Walk and Run
Once participants are eligible, they will undergo the experimental procedure. Before data collection, they will walk or run on a treadmill in barefoot for ten minutes to adapt the condition. The a gait analysis system will collect the data while they walk or run on the treadmill in barefoot at selected gait speed.

What is the study measuring?

Primary Outcome Measures

Primary Outcome Measures

In a clinical study's protocol, the planned outcome measure that is the most important for evaluating the effect of an intervention/treatment. Most clinical studies have one primary outcome measure, but some have more than one.
Outcome Measure
Measure Description
Time Frame
Kinematic characteristics of the the six-degree-of-motion (6DOF) of the gait at initial contact.
Time Frame: 1 Day
The 6DOF include flexion/extension, internal/external rotation, varus/valgus, anterior/posterior translation, medial/ lateral translation, proximal/distal translation.
1 Day
Kinematic characteristics of the the six-degree-of-motion (6DOF) of the gait at loading response.
Time Frame: 1 Day
The 6DOF include flexion/extension, internal/external rotation, varus/valgus, anterior/posterior translation, medial/ lateral translation, proximal/distal translation.
1 Day
Kinematic characteristics of the the six-degree-of-motion (6DOF) of the gait at mid-stance.
Time Frame: 1 Day
The 6DOF include flexion/extension, internal/external rotation, varus/valgus, anterior/posterior translation, medial/ lateral translation, proximal/distal translation.
1 Day
Kinematic characteristics of the the six-degree-of-motion (6DOF) of the gait at terminal stance.
Time Frame: 1 Day
The 6DOF include flexion/extension, internal/external rotation, varus/valgus, anterior/posterior translation, medial/ lateral translation, proximal/distal translation.
1 Day
Kinematic characteristics of the the six-degree-of-motion (6DOF) of the gait at initial swing.
Time Frame: 1 Day
The 6DOF include flexion/extension, internal/external rotation, varus/valgus, anterior/posterior translation, medial/ lateral translation, proximal/distal translation.
1 Day
Kinematic characteristics of the the six-degree-of-motion (6DOF) of the gait at mid-swing.
Time Frame: 1 Day
The 6DOF include flexion/extension, internal/external rotation, varus/valgus, anterior/posterior translation, medial/ lateral translation, proximal/distal translation.
1 Day
Kinematic characteristics of the the six-degree-of-motion (6DOF) of the gait at terminal swing.
Time Frame: 1 Day
The 6DOF include flexion/extension, internal/external rotation, varus/valgus, anterior/posterior translation, medial/ lateral translation, proximal/distal translation.
1 Day
The ranges of motion in the the six-degree-of-motion (6DOF) of the gait.
Time Frame: 1 Day
The 6DOF include flexion/extension, internal/external rotation, varus/valgus, anterior/posterior translation, medial/ lateral translation, proximal/distal translation.
1 Day

Collaborators and Investigators

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

Sponsor

Sponsor

The organization or person who initiates the study and who has authority and control over the study.
Guangzhou General Hospital of Guangzhou Military Command

Collaborators

Collaborators

An organization other than the sponsor that provides support for a clinical study. This support may include activities related to funding, design, implementation, data analysis, or reporting.
The First Affiliated Hospital of Guangzhou Medical University
Medical Center of Assessment, Prevention and Treatment of Bone & Joint Diseases, Guangdong, China

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

Study Start

The actual date on which the first participant was enrolled in a clinical study. The "anticipated" study start date is the date that the researchers think will be the study start date.
January 1, 2017

Primary Completion (Anticipated)

Primary Completion

The date on which the last participant in a clinical study was examined or received an intervention to collect final data for the primary outcome measure. Whether the clinical study ended according to the protocol or was terminated does not affect this date. For clinical studies with more than one primary outcome measure with different completion dates, this term refers to the date on which data collection is completed for all the primary outcome measures. The "anticipated" primary completion date is the date that the researchers think will be the primary completion date for the study.
February 1, 2017

Study Completion (Anticipated)

Study Completion

The date on which the last participant in a clinical study was examined or received an intervention/treatment to collect final data for the primary outcome measures, secondary outcome measures, and adverse events (that is, the last participant's last visit). The "anticipated" study completion date is the date that the researchers think will be the study completion date.
February 1, 2017

Study Registration Dates

First Submitted

First Submitted

The date on which the study sponsor or investigator first submitted a study record to ClinicalTrials.gov. There is typically a delay of a few days between the first submitted date and the record's availability on ClinicalTrials.gov (the first posted date).
January 3, 2017

First Submitted That Met QC Criteria

First Submitted That Met QC Criteria

The date on which the study sponsor or investigator first submits a study record that is consistent with National Library of Medicine (NLM) quality control (QC) review criteria. The sponsor or investigator may need to revise and submit a study record one or more times before NLM's QC review criteria are met. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
January 3, 2017

First Posted (Estimate)

First Posted

The date on which the study record was first available on ClinicalTrials.gov after National Library of Medicine (NLM) quality control (QC) review has concluded. There is typically a delay of a few days between the date the study sponsor or investigator submitted the study record and the first posted date.
January 5, 2017

Study Record Updates

Last Update Posted (Estimate)

Last Update Posted

The most recent date on which changes to a study record were made available on ClinicalTrials.gov. There may be a delay between when the changes were submitted to ClinicalTrials.gov by the study's sponsor or investigator (the last update submitted date) and the last update posted date.
January 5, 2017

Last Update Submitted That Met QC Criteria

Last Update Submitted That Met QC Criteria

The most recent date on which the study sponsor or investigator submitted changes to a study record that are consistent with National Library of Medicine (NLM) quality control (QC) review criteria. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
January 3, 2017

Last Verified

Last Verified

The most recent date on which the study sponsor or investigator confirmed the information about a clinical study on ClinicalTrials.gov as accurate and current. If a study with a recruitment status of recruiting; not yet recruiting; or active, not recruiting has not been confirmed within the past 2 years, the study's recruitment status is shown as unknown.
January 1, 2017

More Information

Terms related to this study

Keywords

Other Study ID Numbers

Other Study ID Numbers

Identifiers or ID numbers other than the NCT number that are assigned to a clinical study by the study's sponsor, funders, or others. These numbers may include unique identifiers from other trial registries and National Institutes of Health grant numbers.
  • GuangzhouGH005

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

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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