- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03855839
The Effect of Posture Shirts on Posture During Functional Tasks
March 4, 2019 updated by: University College of Northern Denmark
The Effect of Posture Shirts on Posture During Functional Tasks in Healthy Participants.
This study investigates the effect of a posture shirt on posture during functional tasks such as office work.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Poor posture have historically been blamed for pain and disability in the general population.
A treatment-strategy that have gain popularity in recent years is the use of a posture shirt which is a compressive shirt designed and marketed to the general public and health service providers as a way to improve posture and consequently alter muscle activity, reduce musculoskeletal pain and discomfort.
This study will investigate the effect of posture shirts on posture.
Study Type
Observational
Enrollment (Actual)
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 Locations
-
-
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Aalborg, Denmark, 9220
- Department of Physiotherapy, University College of Northern Denmark
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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
18 years to 50 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Sampling Method
Non-Probability Sample
Study Population
Healthy male participants
Description
Inclusion Criteria: - Healthy participants
- Pain free healthy participants
- Able to speak, read and understand Danish Exclusion Criteria: - Healthy participants
- Pain from the back, neck or shoulder area during the past 3 months
- Any discomfort in relation to computer use
- Lack of ability to cooperate
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
- Observational Models: Other
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Healthy participants
Participants will be ask to perform a repetitive upper limb task while posture is being monitored.This will be done while wearing a posture shirt, compression shirt or no shirt.
|
Posture shirts are designed, and marketed to the general public and health service providers to improve posture and consequently alter muscle activity, reduce musculoskeletal pain and discomfort.
Compression shirts are designed for recreational sport activities and can be bought in any local sports store
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Posture
Time Frame: Within session (2hr)
|
Posture will be determined by measuring head and shoulder angles during a functional task
|
Within session (2hr)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Experienced pain
Time Frame: Within session (2hr)
|
Any potential pain during the functional tasks will be monitored using a 0-11 numeric rating scale (NRS) with 0 being no pain and 10 being worst imaginable pain.
|
Within session (2hr)
|
|
Concentration during task
Time Frame: Within session (2hr)
|
Two questions regarding concentration during task was asked: (Q1: I had to concentrate to do the task, Q2: My concentration was constant throughout the task) were scores using a 5 point Likert scale (1: Strongly disagree; 2: Disagree; 3: Neither agree nor disagree; 4: Agree; 5: Strongly agree).
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Within session (2hr)
|
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Consciousness of posture during task
Time Frame: Within session (2hr)
|
Two questions regarding consciousness of posture during task was asked (Q1: I was conscious about how I was sitting in the beginning of the task , Q2: I was conscious about how I was sitting at the end of the task) was scored using a 5 point Likert scale (1: Strongly disagree; 2: Disagree; 3: Neither agree nor disagree; 4: Agree; 5: Strongly agree).
|
Within session (2hr)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Steffan W Christensen, PhD, Department of Physiotherapy, University College of Northern Denmark
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)
April 26, 2018
Primary Completion (Actual)
May 8, 2018
Study Completion (Actual)
May 8, 2018
Study Registration Dates
First Submitted
February 13, 2019
First Submitted That Met QC Criteria
February 24, 2019
First Posted (Actual)
February 27, 2019
Study Record Updates
Last Update Posted (Actual)
March 5, 2019
Last Update Submitted That Met QC Criteria
March 4, 2019
Last Verified
February 1, 2019
More Information
Terms related to this study
Other Study ID Numbers
- FOU-UU-2018-12_Sub-project1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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