- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03444285
Effects of Warm up in Athletes With Previous Hamstring Injury
September 27, 2020 updated by: Javier Gutiérrez Coronado, University of Extremadura
Analysis on the Effects of Two Types of Warm up in Athletes With a Previous Hamstring Injury
The objectives of this study is to determine the immediate and 10 minutes follow-up effects of a warm-up based on a continous run on a treadmill or the application of a hot-pack in athletes with previous hamstring injury.
The investigators have as an hypothesis that the subjects, after one of this interventions show statistically significant improvements in the measurements of pain, flexibility, proprioception and postural control
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
62
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
-
-
-
Badajoz, Spain, 06071
- Universidad de Extremadura
-
-
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 to 27 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- To be 18-27 years old
- To do sports as a minimum of 5 hours per week.
- To have done sport in the last 2 years
- Have a hamstring flexibility of ≤80º on Kendall test
- Diagnosed hamstring injury the last year
Exclusion Criteria:
- To take drugs that alter the motor o postural control
- To do a program of stretching of the hamstring
- To have lumbar pain
- Recent abdominal or spinal surgery intervention
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: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Warm Up
|
Run on a treadmill during 10 minutes without fatigue of the participant after this time.
|
|
Active Comparator: Hot Pack
|
20 minutes of hot-pack on both hamstring
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Range of movement
Time Frame: Changes from baseline at immediately after and at 10 minutes after the intervention
|
degrees
|
Changes from baseline at immediately after and at 10 minutes after the intervention
|
|
Pain
Time Frame: Changes from baseline at immediately after and at 10 minutes after the intervention
|
Visual Analogue Scale.
From 0 (not pain) to 10 (maximum pain in the world)
|
Changes from baseline at immediately after and at 10 minutes after the intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pressure pain threshold (PPT)
Time Frame: Changes from baseline at immediately after and at 10 minutes after the intervention
|
Measurement of the pressure (kg/cm2) with an algometer
|
Changes from baseline at immediately after and at 10 minutes after the intervention
|
|
Joint Position Sense
Time Frame: Changes from baseline at immediately after and at 10 minutes after the intervention
|
Degrees
|
Changes from baseline at immediately after and at 10 minutes after the intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Study Director: Javier Gutiérrez Coronado, Physioterapist
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 (Actual)
November 13, 2017
Primary Completion (Actual)
December 4, 2017
Study Completion (Actual)
July 23, 2019
Study Registration Dates
First Submitted
February 2, 2018
First Submitted That Met QC Criteria
February 18, 2018
First Posted (Actual)
February 23, 2018
Study Record Updates
Last Update Posted (Actual)
September 30, 2020
Last Update Submitted That Met QC Criteria
September 27, 2020
Last Verified
September 1, 2020
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 19731973
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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