ClinicalTrials.gg
Not yet recruitingNCT07802782Updated Nov 3, 2026

Core Strength Training, Anthropometry, and Postural Control in Youth Optimist Sailors

An interventional study of Core Strength Training (CST) and Technical Sailing Training (TST) in Postural Control, Athletic Performance and Physical Fitness, sponsored by University of Foggia. Not yet recruiting at 1 site in Italy. Open to participants aged 8 Years to 15 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-11-03.

Sponsored by University of Foggia · Not applicable, Interventional, and Prevention

Updated Nov 3, 2026Start date movedPrimary completion moved+1 moreGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
8 Years to 15 Years
Sex
All
01

Study summary

Optimist dinghy sailing is a highly demanding youth watersport characterized by prolonged, high-intensity isometric hiking postures and rapid dynamic weight shifts required to preserve boat trim, balance, and sail power output. The core (lumbar-pelvic-hip complex) functions as the central dynamic link in transferring kinetic forces between the lower limbs and trunk during continuous open-water maneuvers. This study is designed as a 12-week randomized controlled interventional trial to evaluate the effects of a periodized, circuit-based Core Strength Training (CST) program integrated into routine Technical Sailing Training (TST) compared to TST alone. Primary endpoints evaluate adaptations in the anthropometric profile (skinfold thickness, circumferences, muscle mass percentage) and postural control parameters (Center of Pressure displacement and sway velocity measured via computerized force platform posturography) in competitive youth Optimist sailors.

Read the detailed description

During upwind sailing ("hiking"), Optimist sailors suspend their torso over the windward gunwale, secured only by foot straps over their feet and ankles. This exertion demands sustained isometric contractions of the anterior core, rectus abdominis, quadriceps, and pelvic stabilisers. Inadequate core muscle endurance and deficient postural control compromise boat handling efficiency, accelerate central and peripheral fatigue, and elevate the risk of chronic lower back disorders in young athletes.

Participants will be randomly assigned (1:1 ratio) to either:

Experimental Group (CST+TST): Participating in a 12-week standardized CST program (3 sessions per week) in addition to regular Technical Sailing Training (TST).

Active Control Group (TST Alone): Participating exclusively in the standardized Technical Sailing Training (TST) program (3-4 hours per session, 3 sessions per week).

The CST program progresses systematically across four 2-week meso-blocks, transitioning from foundational bodyweight stability (Weeks 1-6) to advanced dynamic overload and multi-planar surface instability using small fitness tools (Weeks 7-12), such as fit balls, dumbbells, weight discs, resistance bands, Bosu balance trainers, TRX suspension straps, kettlebells, and ankle/wrist weights.

02

Conditions studied

  • Postural Control
  • Athletic Performance
  • Physical Fitness
  • Core Stability

Keywords

  • optimistic sailing
  • Core Strength Training
  • Anthropometry
  • Youth Athletes
  • Posturography
  • McGill Protocol
03

In context

Lead sponsor

University of Foggia is the lead sponsor of 36 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
8 Years to 15 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Active competitive youth Optimist class dinghy sailors aged between 8 and 15 years.
  • Minimum of 2 consecutive years of continuous competitive sailing experience registered with a recognized national sailing federation or licensed sailing club.
  • Regular participation in a minimum of 3 technical sailing sessions per week.
  • Valid sports medical clearance certificate authorizing participation in competitive athletic training.
  • Signed written provided by parent(s) or legal guardian(s), accompanied by written informed assent from the participant.

Exclusion criteria

Exclusion Criteria:

  • Acute or chronic musculoskeletal injuries affecting the spine, abdominal wall, lower limbs, or upper extremities within the preceding 6 months.
  • Concurrent participation in structured external core or strength training programs outside the trial protocol during the preceding 3 months.
  • Neurological, vestibular, or uncorrected visual impairments affecting balance, posturography, or postural control.
  • Training adherence rate below 85% of total prescribed sessions over the 12-week interventional period.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
40 participants (estimated)

Study arms

  • Experimental
    Experimental Group (CST+TST)

    12-week standardized Core Strength Training (CST) program (3 sessions per week) integrated into routine Technical Sailing Training (TST).

    Behavioral: Core Strength Training (CST) · Behavioral: Technical Sailing Training (TST)

  • Active comparator
    Active Control Group (TST Alone)

    12-week standardized Technical Sailing Training (TST) program alone (3-4 hours per session, 3 sessions per week).

    Behavioral: Technical Sailing Training (TST)

Interventions

  • BehavioralCore Strength Training (CST)

    12-week periodized, circuit-based core training (3 sessions/week, 8 stations, 3 sets, \~30 min/session) progressing from foundational bodyweight stability to dynamic overload and surface instability.

  • BehavioralTechnical Sailing Training (TST)

    Standardized open-water technical sailing training (3-4 hours/session, 3 sessions/week) focusing on hiking postures, boat-handling drills, tactical training, and balance optimization.

06

What researchers measure

Primary outcomes

  1. Static Postural Control: Center of Pressure (CoP) Total Path Length Measured via Computerized Force Platform

    Total length of the Center of Pressure (CoP) path (expressed in millimeters) recorded during static standing posturography testing under open-eyes and closed-eyes conditions.

    Time frame: Baseline (Week 0) and Post-Intervention (Week 12)

  2. Static Postural Control: Center of Pressure (CoP) Mean Velocity Measured via Computerized Force Platform

    Mean velocity of Center of Pressure (CoP) displacement (expressed in millimeters per second) recorded during static standing posturography under open-eyes and closed-eyes conditions.

    Time frame: Baseline (Week 0) and Post-Intervention (Week 12)

  3. Static Postural Control: Center of Pressure (CoP) 95% Confidence Ellipse Area Measured via Computerized Force Platform

    Surface area of the 95% confidence ellipse of CoP sway (expressed in square millimeters) recorded during static standing posturography.

    Time frame: Baseline (Week 0) and Post-Intervention (Week 12)

  4. Dynamic Postural Control: Center of Pressure (CoP) Sway Velocity Measured via Computerized Force Platform

    Center of Pressure (CoP) mean sway velocity (expressed in millimeters per second) measured during dynamic unstable platform oscillations and unipedal stance.

    Time frame: Baseline (Week 0) and Post-Intervention (Week 12)

  5. Skinfold Thickness Sum Measured via Skinfold Caliper

    Sum of skinfold thickness measurements (expressed in millimeters) taken at four sites: triceps, subscapular, suprailiac, and abdominal.

    Time frame: Baseline (Week 0) and Post-Intervention (Week 12)

  6. Muscle Mass Percentage Measured via Anthropometric Assessment

    Percentage of total body muscle mass (expressed as % of total body mass) calculated from anthropometric equations.

    Time frame: Baseline (Week 0) and Post-Intervention (Week 12)

  7. Body Fat Mass Percentage Measured via Anthropometric Assessment

    Percentage of total body fat mass (expressed as % of total body mass) calculated from skinfold thickness measurements.

    Time frame: Baseline (Week 0) and Post-Intervention (Week 12)

  8. Waist Circumference Measured via Anthropometric Tape

    Trunk abdominal waist circumference (expressed in centimeters) measured with a flexible metric tape.

    Time frame: Baseline (Week 0) and Post-Intervention (Week 12)

Secondary outcomes

  1. Core Muscle Endurance

    McGill Protocol Battery: Flexor Endurance Test, Biering-Sørensen Extensor Test, Right \& Left Side Bridge Tests measured in seconds.

    Time frame: Baseline (Week 0), Mid-Point (Week 6), and Post-Intervention (Week 12)

  2. Dynamic Balance

    Y-Balance Test / Star Excursion Balance Test (SEBT) normalized reach distances (% leg length).

    Time frame: Baseline (Week 0) and Post-Intervention (Week 12)

07

Study locations

1 site
  • Outdoor Open-Water Sailing Facility & High-Performance Athletic Training Center
    Foggia, FG 71122, Italy
08

References and documents

Individual participant data

Plan to share: Yes — De-identified individual participant data (anthropometric and posturographic parameters) will be available upon reasonable request to the corresponding author for research purposes.

Supporting information: Study protocol, Statistical analysis plan, Informed consent form, Clinical study report, Analytic code

Time frame: Data will be available starting 6 months following publication for up to 3 years.

Access criteria: Researchers whose proposed use of the data has been approved by an independent review committee.

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedDate before it movedWhere the date was before it moved

Start is estimated for Dec 2026; primary completion for Apr 2027, 4 months later.

Since we started tracking on Sep 25, 2026, the dates moved once, on Nov 3, 2026: start Sep 2026 → Dec 2026, primary completion Dec 2026 → Apr 2027 and completion Jan 2027 → May 2027.

Earlier changes are on the record history on ClinicalTrials.gov ↗

How these figures are worked out, and which studies are left out of them.

Registered
Aug 27, 2026
First posted
Sep 3, 2026
StartEst.
Dec 2026was Sep 2026
Primary completionEst.
Apr 2027was Dec 2026
CompletionEst.
May 2027was Jan 2027
Last update
Nov 3, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Start date
Sep 2026→Dec 2026
Nov 3, 2026
Primary completion
Dec 2026→Apr 2027
Nov 3, 2026
Study completion
Jan 2027→May 2027
Nov 3, 2026
Show all 1 update
  1. Nov 3, 2026
    Start date Sep 2026→Dec 2026
    Primary completion Dec 2026→Apr 2027
    Study completion Jan 2027→May 2027
    + 1 other change: verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07802782
Lead sponsor
University of Foggia
Responsible party
Anna Antonia Valenzano (Prof., University of Foggia) — Principal investigator
First posted
Sep 3, 2026
Start date
Dec 2026 (estimated)
Primary completion
Apr 2027 (estimated)
Completion
May 2027 (estimated)
Last update
Nov 3, 2026

Study contacts

Anna A. Valenzano, Prof.
Contact
anna.valenzano@unifg.it
+39 347 6401054

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Nov 2026. You cannot join it, but the record below documents what was studied.

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