Changes in Trunk Stability Indicators Following Two Types of Exhausting Physical Activities
NCT ID: NCT03529734
Last Updated: 2018-05-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
110 participants
INTERVENTIONAL
2018-06-01
2018-10-30
Brief Summary
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In these study 100 subjects will be studied, divided into two groups. First group will perform an exhaustive running protocol and the second group a localized trunk muscle strengthening protocol until exhaustion. The effect of intervention will be studied by observing the changes in trunk muscle reflex responses following sudden arm loading and changes in anticipated trunk muscle activation during a quick arm raising task. Activation latencies and electromyographic (EMG) amplitude, and center of foot pressure excursion will be used to quantify trunk stability. In addition, center of pressure movement during a sitting balance task will be studied as to gather information of local trunk stabilization functions. Finally, changes in joint position sense will be assessed in order to account for the possible changes in kinesthesia.
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Detailed Description
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It is of most relevance for sports trainers and health care community dealing with athletes to be familiar with the effects of exhaustive running and localized trunk muscle fatigue on trunk and spinal stability in order to be better suited in preventing low back pain. This understanding will enable preparation of more suited training plans, periodization and individualization approaches.
This study will recruit volunteers form local university. Each participant will receive his own identification code that will be known only to the principal investigator. In order to account for the possible bias of the investigators, these will not be allowed to participate in assessing subject, which they are familiar with. Six investigators will participate, all trained in performing the measurement and fatiguing protocols.
All participants will be familiarized with the measurement tasks to overcome possible misunderstandings during the study and to ensure most fluent execution of the measurement protocol. The familiarization will account for as much time as needed for the participants to become proficient in each assessment task. Each participant will sigh an informed consent form that will be prepared in accordance with declaration of Helsinki.
Prior to starting the measurements, each subject will perform a worm-up. The measurement will follow in a predefined order, starting with the EMG electrode placement. First subjects will (ii) perform measurements of trunk muscles reflex responses during a sudden hand loading, followed by (iii) measurements of anticipatory postural adjustments during a quick arm rising test, (iv) body sway during a sitting balance tasks, (v) joint position test and (vi) measurements of maximal voluntary contraction for trunk extension and flexion in a neutral upright stance. Next, subjects will perform a fatiguing protocol. One group of subjects will perform a twelve-minute running test (Coopers test) with the goal to cower as much distance as possible. Subjects in the second group will perform dynamic strengthening exercises (curl-up, right lateral trunk flexion, trunk extension and left lateral trunk flexion), each session performed until exhaustion. All together subjects in a dynamic strengthening group will perform three sets with minimal rest in between. Immediately after finishing the fatiguing protocol, the above measurement protocol will be repeated in the same order.
The measurement data will be saved to a personal computers encoded with the subject's identification code. During data acquisition, processing, statistical analysis and data presentation only identification codes will be used. No individual data will be presented. All data will be gathered in a common data sheet for further statistical analysis.
Prior to performing the study, the sample size will be calculated based on the effect size of data gathered during a pilot study using 10 subjects. For main results, fallowing statistics will be calculated:
* Descriptive statistics.
* For parameters not normally distributed, appropriate corrections will be made.
* Intra-group differences prior to fatiguing protocol will be identified using the T-test for independent samples.
* For parameters, where no baseline differences between the two groups were observed, a Two-way repeated measures ANOVA model will be used to observe the possible changes after fatiguing protocols and possible interaction effects for the two groups. Observed differences will be additionally studied with post-hock tests.
* In cases where the baseline status between the two groups will be different, ANCOVA model will be used.
* Correlations between the parameters will be studied using Pearson correlation coefficient.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
NONE
Study Groups
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12 min running group
This group will perform a 12 min high intensity running with the goal to cover maximal possible distance.
12 min running
This was already explained in the description of arm
Local strengthening exercise group
This group will perform local strengthening exercises (curl-ups, left side trunk flexion, trunk extension, right side trunk flexion). Each participant will have to perform three sets of each exercise with the maximal possible number of repetitions with a slow tempo (1s concentric phase and 2 s eccentric phase). Between sets, minimal rest (15 s) will be administered.
Local strengthening exercises
This was already explained in the description of arm
Interventions
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12 min running
This was already explained in the description of arm
Local strengthening exercises
This was already explained in the description of arm
Eligibility Criteria
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Inclusion Criteria
* Age between 20 and 30 years
Exclusion Criteria
* Acute injury of the loco-motor system in the last 1.5 years
* Neurological disease or injury
* Balance related pathology
* Vision pathology or untreated vision deficits
20 Years
30 Years
ALL
Yes
Sponsors
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S2P, Science to Practice, Ltd.
OTHER
Motus Melior
UNKNOWN
University of Primorska
OTHER
Responsible Party
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Nejc Sarabon
Assoc. Prof. Dr. Sc.
Locations
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University of Primorska
Izola, , Slovenia
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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UP-FVZ-Fatigue&TrunkStability
Identifier Type: -
Identifier Source: org_study_id
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