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Clinical Trial Summary

The primary objective of this study is to determine the immediate efficiency of a six weeks regular stretching protocol on regional and distant pain sensitivity. It is hypothesised that regional and distant pain sensitivity will significantly decrease following six weeks of regular stretching. The secondary objective of the study is to determine the effect after four-week cessation of the stretching protocol on regional and distant pain sensitivity. If regional and distant pain sensitivity decrease following regular stretching, it is hypothesised that the analgesic effect will abate following four-week cessation.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04919681
Study type Interventional
Source University College of Northern Denmark
Contact
Status Completed
Phase N/A
Start date November 4, 2021
Completion date October 20, 2022

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