Influence of Latent Miofascial Trigger Points in the Vertical Jump in Female Voleyball Players (LMTP_Volley)

September 16, 2021 updated by: University of Castilla-La Mancha
To evaluate the effects of dry needling of latent myofascial trigger points on vertical jump height in female volleyball players

Study Overview

Detailed Description

Evaluate a sample of female volleyball players after using dry needling on latent myofascial trigger points and verify if it would have an improvement of the vertical jump

Study Type

Interventional

Enrollment (Anticipated)

50

Phase

  • Not Applicable

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

      • Toledo, Spain, 45007
        • Alberto Sánchez Sierra

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 and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • Healthy female volleyball players
  • No Lower limbs injuries in the last 6 months
  • Presence of latent trigger points in gastrocnemius
  • Familiar with performing CMJ test

Exclusion Criteria:

  • Active trigger points in the lower limbs
  • Any contraindication of usind dry needling
  • Any pathology that prevented the performance of CMJ test

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

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Needly Group
Once the trigger point has been identified, we will use the Hong tecnique looking for a local spasm response
Once the trigger point has been identified, we will use the Hong tecnique looking for a local spasm response
Active Comparator: Control Group
Normal volleyball training
Normal volleyball training

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Vertical Jump
Time Frame: pre-intervention
Vertical jump will be measured CMJ test using the app My Jump 2
pre-intervention
Vertical Jump
Time Frame: Immediately post-intervention
Vertical jump will be measured CMJ test using the app My Jump 2
Immediately post-intervention
Vertical Jump
Time Frame: 72 hours post-intervention
Vertical jump will be measured CMJ test using the app My Jump 2
72 hours post-intervention
Vertical Jump
Time Frame: one week post-intervention
Vertical jump will be measured CMJ test using the app My Jump 2
one week post-intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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 (Anticipated)

October 15, 2021

Primary Completion (Anticipated)

January 15, 2022

Study Completion (Anticipated)

January 15, 2022

Study Registration Dates

First Submitted

September 16, 2021

First Submitted That Met QC Criteria

September 16, 2021

First Posted (Actual)

September 28, 2021

Study Record Updates

Last Update Posted (Actual)

September 28, 2021

Last Update Submitted That Met QC Criteria

September 16, 2021

Last Verified

September 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • Sánchez-Sierra1

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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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