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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04161105
Other study ID # DomMSc
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 16, 2019
Est. completion date November 29, 2019

Study information

Verified date February 2020
Source Institute of Technology, Carlow
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study evaluates the impact of treating myofascial trigger points with a single session of dry needling on maximal isometric strength in the short term. Two groups will receive dry needling in separate muscle groups and a third group will receive no dry needling.


Description:

Dry needling is a effective treatment for myofascial trigger points. It is very common in a sporting environment. Strength is a key aspect of athletic performance. Despite the prevalence of dry needling within a sporting environment, the effects of dry needling on strength remains unknown.

This study will investigate the effects of dry needling on maximal isometric strength with a view to informing clinical practice amongst clinicians working in the elite sport setting.


Recruitment information / eligibility

Status Completed
Enrollment 28
Est. completion date November 29, 2019
Est. primary completion date November 29, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria:

- Must have latent trigger points in their rectus femoris and gluteus maximus

Exclusion Criteria:

- Active trigger points in rectus femoris or gluteus maximus

- Participants with current injuries

- History of fibromyalgia or myofascial pain syndrome

- History of blood disorder which prevents dry needling

- Needle phobia

- History of surgery in the last 6 months

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Dry needling
Dry needling is an invasive procedure involving inserting acupuncture needles directly into trigger points within muscles. The needle is partially withdrawn and re-inserted repeatedly to maximally stimulate the muscle and it's fibers.

Locations

Country Name City State
Ireland Institute of Technology Carlow Carlow Leinster

Sponsors (1)

Lead Sponsor Collaborator
Institute of Technology, Carlow

Country where clinical trial is conducted

Ireland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Isometric peak force during the isometric mid-thigh pull Measured in newtons. It is the amount of force exerted by pulling against an immovable bar. Peak force is measured as vertical ground reaction by force platforms beneath the participants feet. Baseline, 24 hours post intervention, 48 hours post intervention, 72 hours post intervention.
Primary Isometric peak rate of force development during the isometric mid-thigh pull Measured in newtons per second squared. It is the amount of force exerted by pulling against an immovable bar divided by the amount of time it takes to generate the force. It is measured as vertical ground reaction by force platforms beneath the participants feet. Baseline, 24 hours post intervention, 48 hours post intervention, 72 hours post intervention.
Primary Relative isometric peak force during the isometric mid-thigh pull Measured in newtons per kg body weight. It is the amount of force exerted by pulling against an immovable bar divided by two thirds the participants body weight. Peak force is measured as vertical ground reaction by force platforms beneath the participants feet. Baseline, 24 hours post intervention, 48 hours post intervention, 72 hours post intervention.
Primary Relative isometric peak rate of force development during the isometric mid-thigh pull Measured in newtons per second squared per kg. It is the amount of force exerted by pulling against an immovable bar divided by the amount of time it takes to generate the force divided by two thirds the participants body weight. It is measured as vertical ground reaction by force platforms beneath the participants feet. Baseline, 24 hours post intervention, 48 hours post intervention, 72 hours post intervention.
Primary Normalised isometric peak rate of force development during the isometric mid-thigh pull Measured in newtons per second squared and expressed relative to each participant peak force. It is the amount of force exerted by pulling against an immovable bar divided by the amount of time it takes to generate the force divided by the peak vertical ground reaction force produced during the trial. It is measured as vertical ground reaction by force platforms beneath the participants feet. Baseline, 24 hours post intervention, 48 hours post intervention, 72 hours post intervention.
Primary Isometric time interval rate of force development during the isometric mid-thigh pull Measured in newtons per second squared. It is the amount of force exerted by pulling against an immovable bar divided by the amount of time it takes to generate the force. With values expressed in specific time interval windows (0ms to 50ms, 0-100ms, 0-150ms, 0-200ms, 0-250ms) It is measured as vertical ground reaction by force platforms beneath the participants feet. Baseline, 24 hours post intervention, 48 hours post intervention, 72 hours post intervention.
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