Skip to main content
Clinical Trials/NCT04600830
NCT04600830
Completed
N/A

Evaluation of the Effectiveness of Dry Needling Against Foam Roller in the Short Term, Healthy Athletes With Reduced Mobility of the Ankle Joint

Fundación Universidad Católica de Valencia San Vicente Mártir1 site in 1 country45 target enrollmentMay 1, 2020

Overview

Phase
N/A
Intervention
Not specified
Conditions
Myofascial Pain Syndromes
Sponsor
Fundación Universidad Católica de Valencia San Vicente Mártir
Enrollment
45
Locations
1
Primary Endpoint
Range of motion (ROM)
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

To compare the effects of dry needling and Foam roller in myofascial trigger points. Needling has been shown to decrease pain in the short term; however, its effects on muscle force production are unclear. There are differences between dry needling and foam roller after treatment?

Detailed Description

Background: It has been shown that the decrease of the range of motion in the ankle, due to the presence of latent trigger points in the gastro-sole complex, can affect performance, as well as being a predisposing factor to injury. Objective: To compare the effects of Dry Needling and Foam roller in healthy athletes with limited dorsal ankle flexion by the presence of latent trigger points. Material and methods: This is a clinical trial, single-blind experimental study. The sample will have a total of 44 students, volunteers, healthy of the degree of physiotherapy of the the investigator's university (UCV). Participants who meet the inclusion criteria will be randomly assigned in two groups: Group 1 or Dry Needling (N = 22) and Group 2 or Foam Roller (N = 22). The range of motion of ankle will be assessed through the Leg Motion system (Check Your Motion®, Albacete, Spain). Assessed thought Ankle Test (post-intervention and 24 hours later). The reference values to consider the decreased ankle ROM will be \<11.5 cm, \<35º measured with Easy Angle® digital goniometer (Meloq AB, Sweden) and/or if it has a difference of 1.5 cm between both extremities. Thus, the effect on previous activity performance will be assessed thought the Counter Movement Jump. Data analysis: Once the distribution of the sample is determined, a descriptive analysis of the data will be carried out and an ANOVA of repeated measures. Will be used to compare the data found in the two groups that make up the study taking into account a 95% CI and an error less than 0.05.

Registry
clinicaltrials.gov
Start Date
May 1, 2020
End Date
May 10, 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Fundación Universidad Católica de Valencia San Vicente Mártir
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Students of physiotherapy degree of the university
  • All participants who present restriction on active ankle dorsiflexion (\<35º).
  • They must be diagnosed through manual therapy of latent PG in the gastro-soleus complex.

Exclusion Criteria

  • Subjects suffering from belonephobia
  • Pathology of connective tissue
  • Coagulation problems
  • Lymphatic disorders
  • Surgical history in the lower limb (last 12 months)
  • Prior treatment with dry needling (last 6 months)

Outcomes

Primary Outcomes

Range of motion (ROM)

Time Frame: 48 hours

Range of motion (ROM) is a key measurement to help in detecting and diagnosing musculoskeletal deficits, monitoring treatment progression, and guiding the treatment plan. Measurement of ROM is a relevant point and an important item of the joint evaluation process when using any ankle scoring system as part of the ankle and ankle joint evaluation. ROM of ankle joint in load PRE, POST treatment and POST 24 hours after of intervention.

Secondary Outcomes

  • Lunge / Ankle Test Test(48 hours)
  • Counter Movement Jump (CMJ)(48 hours)

Study Sites (1)

Loading locations...

Similar Trials