- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05058625
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
Status
Not yet recruiting
Conditions
Intervention / Treatment
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.
Sponsor
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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