- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03889665
Effects of Suspension Training on the Balance of Healthy Young Adults
November 28, 2022 updated by: Jose María Blasco Igual, University of Valencia
Influencia Del Entrenamiento en suspensión en el Equilibrio de Adultos jóvenes Sanos
Non-specific training through the use of devices in which the subject can be suspended is a technique that has aroused a growing interest in recent years.
One of its advantages may be to enhance the balance, since it induces a high level of neuromuscular stimulation.
Indeed, a suspension training suppose a high demand of the core musculature, require a high degree of postural control, precise response strategies , anticipatory capacity and muscular conditioning.
However, current literature targeting healthy young adults and appraising the specifics effects of suspension training on balance is scarce or non-existent to the best of our knowledge.
For this reason this interventional study will primarily assess the effects of suspension training on different balance components.
Study Overview
Study Type
Interventional
Enrollment (Actual)
39
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
-
-
Valencia
-
València, Valencia, Spain, 46010
- Universitat de Valencia
-
-
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 30 years (ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Healthy young adults aged between 18 and 30
Exclusion Criteria:
- Professional athlete
- Musculoskeletal injury in the last 6 months (i.e. sprain, bone fracture)
- Known balance disorders including vertigo, central or vestibular limitations
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: NA
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: Suspension training group
|
Nine sessions of suspension training The suspension device will be TRX (R) The intervention will be administered in work:rest intervals (2:1) A global training approach will seek to train lower limbs, upper body and core musculature
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Y-Balance test
Time Frame: Change from baseline to four weeks
|
Measure of dynamic balance
|
Change from baseline to four weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Emery test
Time Frame: Change from baseline to four weeks
|
A timed test for static-dynamic balance assessment, the participant stands on one leg over a foam with closed eyes
|
Change from baseline to four weeks
|
Posturography measures
Time Frame: Change from baseline to four weeks
|
Using a T-Plate pedometer
|
Change from baseline to four weeks
|
Jumping sideways test
Time Frame: Change from baseline to four weeks
|
A measure to assess motor coordination under time pressure
|
Change from baseline to four weeks
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Five times sit-to-stand test
Time Frame: Change from baseline to four weeks
|
This is generally used to assess the functional strength of the lower extremities, the transition movements, the balance and the risk of falls are evaluated
|
Change from baseline to four weeks
|
Stabilizer pressure biofeedback
Time Frame: Change from baseline to four weeks
|
This is used to assess core strength
|
Change from baseline to four weeks
|
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 (ACTUAL)
April 1, 2019
Primary Completion (ACTUAL)
May 1, 2019
Study Completion (ACTUAL)
May 31, 2019
Study Registration Dates
First Submitted
March 22, 2019
First Submitted That Met QC Criteria
March 22, 2019
First Posted (ACTUAL)
March 26, 2019
Study Record Updates
Last Update Posted (ACTUAL)
November 29, 2022
Last Update Submitted That Met QC Criteria
November 28, 2022
Last Verified
November 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- TRX-Balance
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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