The Effect of a Posture Shirt on Muscle Activity During Functional Tasks
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| ClinicalTrials.gov Identifier: NCT03855124 |
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Recruitment Status : Unknown
Verified February 2019 by University College of Northern Denmark.
Recruitment status was: Recruiting
First Posted : February 26, 2019
Last Update Posted : March 25, 2019
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| Condition or disease | Intervention/treatment |
|---|---|
| Healthy | Device: Posture shirt |
| Study Type : | Observational |
| Estimated Enrollment : | 30 participants |
| Observational Model: | Other |
| Time Perspective: | Cross-Sectional |
| Official Title: | The Effect of a Posture Shirt on Muscle Activity During Functional Tasks |
| Actual Study Start Date : | March 21, 2019 |
| Estimated Primary Completion Date : | December 31, 2019 |
| Estimated Study Completion Date : | December 31, 2019 |
| Group/Cohort | Intervention/treatment |
|---|---|
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healthy participants
Participants will be ask to perform a repetitive upper limb task while posture and muscle activity is being monitored.This will be done while wearing a posture shirt or without a shirt
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Device: Posture shirt
Posture shirts are designed, and marketed to the general public and health service providers to improve posture and consequently alter muscle actitity, reduce musculoskeletal pain and discomfort. |
- Electromyography (EMG) [ Time Frame: During the test session ]EMG acitivty of axioscapular and trunk muscles will be recorded during upper limb tasks
- Pain intensity: scale [ Time Frame: During the test session ]Participants are to rate any perceived pain on a scale from 0-10 (0=no pain, 10= worst imaginable pain)
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| Ages Eligible for Study: | 18 Years to 50 Years (Adult) |
| Sexes Eligible for Study: | Male |
| Gender Based Eligibility: | Yes |
| Gender Eligibility Description: | Male participants |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- Pain free healthy participants
- Able to speak, read and understand Danish
Exclusion Criteria:
- Pain from the back, neck or shoulder area during the past 6 months
- Experience of delayed onset muscle soreness (DOMS) on the day of testing
- Current or previous chronic or recurrent pain condition
- Regular use of analgesics
- Previous neurologic, musculoskeletal or mental illnesses that may influence the results
- Lack of ability to cooperate
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03855124
| Contact: Steffan W Christensen, PhD | +45 72691009 | sec@ucn.dk |
| Denmark | |
| Department of Physiotherapy, University College of Northern Denmark | Recruiting |
| Aalborg, Denmark, 9220 | |
| Contact: Steffan W Christensen, PhD +45 72691009 sec@ucn.dk | |
| Principal Investigator: | Steffan W Christensen, PhD | Department of Physiotherapy, University College of Northern Denmark |
| Responsible Party: | University College of Northern Denmark |
| ClinicalTrials.gov Identifier: | NCT03855124 |
| Other Study ID Numbers: |
FOU-UU-2018-12_Sub-project2 |
| First Posted: | February 26, 2019 Key Record Dates |
| Last Update Posted: | March 25, 2019 |
| Last Verified: | February 2019 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | Undecided |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Electromyography Musculoskeletal |

