- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05873985
The Acute Effect of Dynamic Taping on Upper Body Posture.
May 22, 2023 updated by: Fuat YÜKSEL, Gazi University
The Acute Effect Of Dynamic Taping Applied To The Neck And Back Region On Upper Body Posture In Asymptomatic Male Individuals
The aim of this study was to evaluate the acute effect of Dynamic tape on cervical and thoracic region posture in asymptomatic male individuals.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Fifty-one asymptomatic individuals between the ages of 18 and 32 years were included in the study.
The participants in this study were randomised into two groups, named "Dynamic Taping" (mean age± sd: 23.28±3.41
yrs, n=25) and "Sham Taping" (mean age± sd: 25.15±4.13
yrs, n=26).
In the Dynamic taping group, tapes were applied with optimal stretching, while in the Sham taping group, tapes were applied without any stretch.
All measurements were done before taping and 30 minutes after taping.
Craniovertebral, cranio-horizontal and sagittal shoulder angles were calculated with photographic posture analysis, while thoracic kyphosis was evaluated with a digital inclinometer (JTech IQ Pro™, ABD).
Study Type
Interventional
Enrollment (Actual)
51
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
-
-
-
Ankara, Turkey
- Gazi University
-
-
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
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- between the ages of 18-40 years,
- male gender,
- not having any injuries to the neck and back region in the last 3 months
Exclusion Criteria:
- Individuals who were allergic to taping,
- had neurological or rheumatological disorders
- felt discomfort after starting the study
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: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Dynamic tape on experimental group
As a result of randomization, dynamic tape was applied to 25 people with a special technique.
|
The dynamic taping application was carried out in 2 stages.
Three "I"-shaped tapes were cut.
In the first stage, the person was asked to perform scapular retraction, and in this position, the tape was placed by applying medium tension to the anterior part of the other deltoid muscle, passing from the anterior part of the deltoid muscle to the upper thoracic region.
In the second stage, the participant was asked to do scapular retraction and depression, and while maintaining this position, medium tension was applied to the lower thoracic vertebra starting from the anterior part of the deltoid muscle and the acromion and tape was applied.
Afterward, this process was applied on the other side
|
|
Placebo Comparator: Sham tape on placebo group
As a result of randomization, dynamic tape was applied to 26people with a sham technique.
|
Sham taping was performed in 2 stages.
Three "I"-shaped tapes were cut.
Participants were asked to stand in the comfortable position they used during the day.
The first tape was adhered from the starting point of the spine of the scapula with the acromion to the junction of the spine of the scapula and the acromion on the other side without any tension.
The other two tapes, starting from the beginning and ending points of the first tape, were adhered to the lower thoracic region without any tension
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Photographic Posture Assessment
Time Frame: 5 minutes before tape
|
To take pictures of the participants, the camera (Logitech, Switzerland) was placed on a tripod with a height of 115 cm and at a distance of 1.5 m (33).
In order to maintain the same distance between the camera and the participants, a spot on the ground was marked for the subjects to stand, and the tripod was fixed to the ground.
The photos were taken of the left side of the subjects in standing position.
Before photographing, reflective markers were placed on the lateral canthus, tragus, 7th cervical vertebra, and acromion.
During the photography, the subjects were asked to stand in a comfortable position as in daily life.
|
5 minutes before tape
|
|
Photographic Posture Assessment
Time Frame: 15 minutes after tape
|
o take pictures of the participants, the camera (Logitech, Switzerland) was placed on a tripod with a height of 115 cm and at a distance of 1.5 m (33).
In order to maintain the same distance between the camera and the participants, a spot on the ground was marked for the subjects to stand, and the tripod was fixed to the ground.
The photos were taken of the left side of the subjects in standing position.
Before photographing, reflective markers were placed on the lateral canthus, tragus, 7th cervical vertebra, and acromion.
During the photography, the subjects were asked to stand in a comfortable position as in daily life.
|
15 minutes after tape
|
|
Cranio-horizontal angle (Before)
Time Frame: 5 minutes before tape
|
Photographs were analysed using the "ImageJ" program and CH angle were calculated and data were recorded.
This procedure was performed by a researcher blinded to the study.
This is the angle between the horizontal line drawn from the tragus and the line drawn from the tragus to the lateral canthus of the eye.
It provides information about the position of the head above the neck and the location of the upper cervical spine.
|
5 minutes before tape
|
|
Cranio-horizontal angle (after)
Time Frame: 15 minutes after tape
|
Photographs were analysed using the "ImageJ" program and CH angle were calculated and data were recorded.
This procedure was performed by a researcher blinded to the study.
This is the angle between the horizontal line drawn from the tragus and the line drawn from the tragus to the lateral canthus of the eye.
It provides information about the position of the head above the neck and the location of the upper cervical spine.
|
15 minutes after tape
|
|
Craniovertebral angle (before)
Time Frame: 5 minutes before tape
|
Photographs were analysed using the "ImageJ" program and CV angle were calculated and data were recorded.
This procedure was performed by a researcher blinded to the study.This is the angle between the horizontal line drawn from the 7th cervical vertebra and the line drawn from the 7th cervical vertebra to the tragus .
The CV angle provides information about the position of the lower cervical region and is used in the objective evaluation of FHP.
|
5 minutes before tape
|
|
Craniovertebral angle (after)
Time Frame: 15 minutes after tape
|
Photographs were analysed using the "ImageJ" program and CV angle were calculated and data were recorded.
This procedure was performed by a researcher blinded to the study.This is the angle between the horizontal line drawn from the 7th cervical vertebra and the line drawn from the 7th cervical vertebra to the tragus .
The CV angle provides information about the position of the lower cervical region and is used in the objective evaluation of FHP.
|
15 minutes after tape
|
|
Sagittal shoulder posture angle ( Before)
Time Frame: 5 minutes before tape
|
Photographs were analysed using the "ImageJ" program and SSP angle were calculated and data were recorded.
This procedure was performed by a researcher blinded to the study.This is the angle between the horizontal line drawn from the acromion and the line connecting the acromion to the 7th cervical vertebra.
This assessment provides information about the position of the shoulder
|
5 minutes before tape
|
|
Sagittal shoulder posture angle (after)
Time Frame: 15 minutes after tape
|
Photographs were analysed using the "ImageJ" program and SSP angle were calculated and data were recorded.
This procedure was performed by a researcher blinded to the study.This is the angle between the horizontal line drawn from the acromion and the line connecting the acromion to the 7th cervical vertebra.
This assessment provides information about the position of the shoulder
|
15 minutes after tape
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Thoracic kyphosis angle (Before)
Time Frame: 5 minutes before tape
|
TK angle was measured with a dual digital inclinometer (JTech IQ Pro™, USA).
Participants were asked to stand in a relaxed position.
The dual inclinometer device was placed over the spinous processes of the 1st thoracic vertebra and the 12th thoracic vertebra.
The measured angle was recorded as the TK angle.
|
5 minutes before tape
|
|
Thoracic kyphosis angle (after)
Time Frame: 15 minutes after tape
|
TK angle was measured with a dual digital inclinometer (JTech IQ Pro™, USA).
Participants were asked to stand in a relaxed position.
The dual inclinometer device was placed over the spinous processes of the 1st thoracic vertebra and the 12th thoracic vertebra.
The measured angle was recorded as the TK angle.
|
15 minutes after tape
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 1, 2022
Primary Completion (Actual)
April 1, 2022
Study Completion (Actual)
May 1, 2022
Study Registration Dates
First Submitted
May 3, 2023
First Submitted That Met QC Criteria
May 22, 2023
First Posted (Actual)
May 24, 2023
Study Record Updates
Last Update Posted (Actual)
May 24, 2023
Last Update Submitted That Met QC Criteria
May 22, 2023
Last Verified
May 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- Efe1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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