Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03443050
Other study ID # UNSTABLE_UV
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 1, 2018
Est. completion date April 4, 2018

Study information

Verified date March 2019
Source University of Valencia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective of this study is to determine the effects on balance and postural control produced by the implementation of a training program that includes work with unstable surfaces in its methods. It also seeks to quantify to what extent the benefits exceed those achieved with a training of similar characteristics, but implemented on a stable surface. An intensive program is proposed, whose target population is young adults.


Recruitment information / eligibility

Status Completed
Enrollment 48
Est. completion date April 4, 2018
Est. primary completion date April 4, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria:

- Healthy young adults aged between 18 and 30

Exclusion Criteria:

- Professional athlete

- Musculoskeletal injury in the last 12 months (i.e. sprain, bone fracture)

- Known balance disorders including vertigo, central or vestibular limitations

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Unstable
This group will train over unstable surfaces to enhance balance abilities
Stable
This group will train over stable surface to enhance balance abilities

Locations

Country Name City State
Spain University of Valencia. Facultat de Fisioterapia Valencia

Sponsors (1)

Lead Sponsor Collaborator
University of Valencia

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Other Jumping sideways test Test of agility. Evaluates motor coordination under the pressure of time of implementation. The jumps in 15 seconds are recorded change from baseline to end of intervention (4weeks)
Other T-agility test Evaluation of the performance of the change of direction, as well as the speed and power of the lower extremities change from baseline to end of intervention (4weeks)
Primary Y-balance test Dynamic balance. The maximum length in cm achieved for each leg in the anterior, posterior-lateral and medial-lateral positions will be recorded. change from baseline to end of intervention (4weeks)
Secondary Posturography (1) A force T-plate platform will be used to assess posture in terms of sway area (mm2) change from baseline to end of intervention (4weeks)
Secondary Posturography (2) A force T-plate platform will be used to assess posture in terms of mean velocity (m/s) change from baseline to end of intervention (4weeks)
Secondary Emery test Static balance and proprioception as measured with the eyes closed to keep balance with one leg over an Airex(R) balance pad. The time in seconds will be recorded. change from baseline to end of intervention (4weeks)
Secondary Functional reach Test of stability, measured as the distance reached when leaning forward without falling (cm) change from baseline to end of intervention (4weeks)
See also
  Status Clinical Trial Phase
Recruiting NCT06052553 - A Study of TopSpin360 Training Device N/A
Completed NCT05511077 - Biomarkers of Oat Product Intake: The BiOAT Marker Study N/A
Recruiting NCT04632485 - Early Detection of Vascular Dysfunction Using Biomarkers From Lagrangian Carotid Strain Imaging
Completed NCT05931237 - Cranberry Flavan-3-ols Consumption and Gut Microbiota in Healthy Adults N/A
Completed NCT04527718 - Study of the Safety, Tolerability and Pharmacokinetics of 611 in Adult Healthy Volunteers Phase 1
Terminated NCT04556032 - Effects of Ergothioneine on Cognition, Mood, and Sleep in Healthy Adult Men and Women N/A
Completed NCT04065295 - A Study to Test How Well Healthy Men Tolerate Different Doses of BI 1356225 Phase 1
Completed NCT04998695 - Health Effects of Consuming Olive Pomace Oil N/A
Completed NCT04107441 - AX-8 Drug Safety, Tolerability and Plasma Levels in Healthy Subjects Phase 1
Completed NCT01442831 - Evaluate the Absorption, Metabolism, And Excretion Of Orally Administered [14C] TR 701 In Healthy Adult Male Subjects Phase 1
Terminated NCT05934942 - A Study in Healthy Women to Test Whether BI 1358894 Influences the Amount of a Contraceptive in the Blood Phase 1
Recruiting NCT05525845 - Studying the Hedonic and Homeostatic Regulation of Food Intake Using Functional MRI N/A
Completed NCT05515328 - A Study in Healthy Men to Test How BI 685509 is Processed in the Body Phase 1
Completed NCT05030857 - Drug-drug Interaction and Food-effect Study With GLPG4716 and Midazolam in Healthy Subjects Phase 1
Completed NCT04967157 - Cognitive Effects of Citicoline on Attention in Healthy Men and Women N/A
Recruiting NCT04494269 - A Study to Evaluate Pharmacokinetics and Safety of Tegoprazan in Subjects With Hepatic Impairment and Healthy Controls Phase 1
Recruiting NCT04714294 - Evaluate the Safety, Tolerability and Pharmacokinetics Characteristics of HPP737 in Healthy Volunteers Phase 1
Completed NCT04539756 - Writing Activities and Emotions N/A
Recruiting NCT04098510 - Concentration of MitoQ in Human Skeletal Muscle N/A
Completed NCT03308110 - Bioavailability and Food Effect Study of Two Formulations of PF-06650833 Phase 1