ClinicalTrials.gg
CompletedNCT07886749CoMTUpdated Oct 26, 2026

Corrective Multisport Training

An interventional study of Corrective multisport training and Multisport (CON) Group in Postural Alignment and Posture, sponsored by University of Novi Sad. Completed at 1 site in Serbia. Open to participants aged 4 Years to 11 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-26.

Sponsored by University of Novi Sad · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Registered 5 years 1 month after the study started (first participant enrolled Sep 2021, registered Oct 2026).
Updated Oct 26, 2026Eligibility revisedPrimary outcomes revised+2 moreGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
398
Allocation
Randomized
Ages
4 Years to 11 Years
Sex
All
01

Study summary

Background: Postural deviations of the shoulders, pelvis and spine are common in preschool and school-aged children and may contribute to musculoskeletal imbalance and pain. Corrective exercise and organised sport have each been shown to benefit posture, but the effect of combining them in a single programme has not been examined.

Aim: To determine the effect of a nine-month corrective multisport (CMS) training programme on upper-body posture in healthy preschool and school-aged children.

Methods: In a single-centre, parallel-group randomised controlled trial, 398 healthy children were randomised (1:1, block randomisation stratified by sex) to a corrective multisport (CMS) group or a control (CON) group. The CMS group completed two 60-minute sessions per week for nine months, combining corrective strength and stretching exercises with multisport activities (soccer, basketball, handball, tennis). The CON group continued regular physical education. Upper-body posture was assessed before and after the intervention with the Contemplas three-dimensional (3D) photogrammetric system (Templo software) by assessors blinded to group allocation.

Read the detailed description

Study design: Single-centre, parallel-group, randomised controlled trial conducted between September 2021 and June 2022 at the Faculty of Sport and Physical Education, University of Novi Sad, Serbia. Participants were allocated 1:1 using a computer-generated block randomisation list stratified by sex, prepared by an independent researcher. Allocation was concealed in sealed, opaque, sequentially numbered envelopes opened after baseline testing. Outcome assessors were blinded to group allocation. The study is reported in accordance with the Consolidated Standards of Reporting Trials (CONSORT) statement, was conducted in accordance with the Declaration of Helsinki, and was approved by the Ethics Committee of the Faculty of Sport and Physical Education, University of Novi Sad (Approval Number 46-06-04/2020-1). Written informed consent was obtained from parents or guardians.

Participants: Children were recruited through an open call to local preschools and elementary schools (September-October 2021). Of 540 children screened, 398 (198 boys, 200 girls) were randomised (corrective multisport [CMS] group, n = 199; control [CON] group, n = 199).

Intervention: The CMS programme lasted nine months (two sessions per week, approximately 60 min each) and was delivered by certified physical education teachers under the supervision of exercise scientists. Each session comprised (I) a 15-min warm-up with posture correction, (II) 20 min of progressive corrective strength and stretching exercises targeting the spinal, trunk, neck and shoulder musculature, (III) 20 min of sport activities (soccer, basketball, handball, tennis) and (IV) a 5-min cool-down. Active Comparator - Multisport (CON) Group received the multisport programme. Participants in this group completed a nine-month multisport programme (two sessions per week, approximately 60 minutes each) delivered by certified physical education and sport teachers without additional kinesiotherapy qualifications.

Measurements: Body height and body mass were measured (SECA 225 stadiometer and SECA 770 digital scale), and body mass index (BMI) was calculated. Upper-body posture was assessed with a calibrated Contemplas three-dimensional (3D) Motion Analysis System (Templo 3D Posture Compact protocol), using retro-reflective markers on 10 anatomical landmarks, within two days before and after the intervention.

02

Conditions studied

  • Postural Alignment
  • Posture

Keywords

  • Corrective exercise
  • Multisport training
  • Upper-body posture
  • Children
  • Physical education
  • Photogrammetry
03

In context

Lead sponsor

University of Novi Sad is the lead sponsor of 28 studies on the registry; 7 are open to participants now.

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

04

Who can participate

The criteria were revised on the registry on Oct 26, 2026. See what changed

Ages eligible
4 Years to 11 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

  • Healthy preschool or primary-school children aged 4-11 years
  • No injuries within the past six months
  • No current acute illness, including Coronavirus Disease 2019 (COVID-19)
  • No scheduled structured physical activity in the previous three months
  • Written from parents/guardians

Exclusion criteria

Exclusion Criteria:

  • History of neurological or musculoskeletal disorders
  • Clinical conditions that could affect balance, such as motor disorders
  • Respiratory disorders (e.g., asthma)
  • Developmental disorders
  • Heart disease, vision problems, or disorders of nerves or blood vessels
  • Clinically diagnosed postural deformities
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

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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
None (open label)
Enrollment
398 participants (actual)

Study arms

  • Experimental
    Corrective multisport (CMS) group

    Corrective multisport training

    Other: Corrective multisport training

  • Active comparator
    Multisport (CON) Group

    Children in this arm received the multisport programme.

    Other: Multisport (CON) Group

Interventions

  • OtherCorrective multisport training

    Nine months, 2 × 60 minutes/week, delivered by certified physical education teachers. Each session: warm-up with posture correction (15 minutes); progressive corrective strength and stretching exercises for the spinal, trunk, neck and shoulder muscles (20 minutes; e.g., cat-cow stretch, wall angels, superman, bird dog, bridge, chin tuck); sport activities: soccer, basketball, handball, tennis (20 minutes); cool-down (5 minutes).

    Also known as: Corrective exercise; Multisport programme

  • OtherMultisport (CON) Group

    Participants in this group completed a nine-month multisport programme (two sessions per week, approximately 60 minutes each) delivered by certified physical education and sport teachers without additional kinesiotherapy qualifications. Weekly content targeted one of three gross motor skill categories: stability (including trunk strengthening), locomotor (e.g., running, hopping, skipping) or manipulative (ball skills). Children were also introduced to basic elements of team and individual sports. Sessions were delivered mainly as circuit and station training using gymnastic apparatus, obstacles and elementary games. Each session comprised a 15-minute warm-up (movements at varying speeds, stretching, and general corrective and preventive exercises for posture and flat feet), a 40-minute main part (practice of previously learned skills, learning of new skills, competitive practice and conditioning) and a 5-minute cool-down.

06

What researchers measure

Primary outcomes

  1. Shoulder displacement

    Displacement of the shoulders in the frontal plane, measured with the Contemplas 3D photogrammetric system (Templo software). Unit of measure: cm.

    Time frame: Baseline and post-intervention (9 months)

  2. Shoulder rotation

    Rotation of the left and right shoulders in the longitudinal axis (transverse plane), Contemplas 3D. Unit of measure: degrees.

    Time frame: Baseline and post-intervention (9 months)

  3. Pelvic rotation

    Rotation of the pelvis in the longitudinal axis (transverse plane), Contemplas 3D. Unit of measure: degrees.

    Time frame: Baseline and post-intervention (9 months)

  4. Pelvic displacement

    Displacement of the pelvis in the frontal plane, Contemplas 3D. Unit of measure: cm.

    Time frame: Baseline and post-intervention (9 months)

  5. Sagittal distance cervical spine-sacrum

    Distance of the most protruded cervical vertebra relative to the vertical projection of the sacrum in the sagittal plane, Contemplas 3D. Unit of measure: cm.

    Time frame: Baseline and post-intervention (9 months)

  6. Sagittal distance thoracic spine-sacrum

    Distance of the thoracic spine relative to the vertical projection of the sacrum in the sagittal plane, Contemplas 3D. Unit of measure: cm.

    Time frame: Baseline and post-intervention (9 months)

  7. Sagittal distance lumbar spine-sacrum

    Distance of the lumbar spine relative to the vertical projection of the sacrum in the sagittal plane, Contemplas 3D. Unit of measure: cm.

    Time frame: Baseline and post-intervention (9 months)

  8. Frontal cervical spine

    Distance of the cervical spine relative to the vertical projection of the sacrum in the frontal plane, Contemplas 3D. Unit of measure: cm.

    Time frame: Baseline and post-intervention (9 months)

  9. Frontal thoracic spine

    Distance of the thoracic spine relative to the vertical projection of the sacrum in the frontal plane, Contemplas 3D. Unit of measure: cm.

    Time frame: Baseline and post-intervention (9 months)

  10. Frontal lumbar spine

    Distance of the lumbar spine relative to the vertical projection of the sacrum in the frontal plane, Contemplas 3D. Unit of measure: cm.

    Time frame: Baseline and post-intervention (9 months)

Secondary outcomes

  1. Body height

    Measured barefoot body height with a SECA 225 stadiometer. Units: centimeters.

    Time frame: Baseline and post-intervention (9 months)

  2. Body mass

    Measured body mass with a SECA 770 digital scale. Units: kilograms.

    Time frame: Baseline and post-intervention (9 months)

07

Study locations

1 site
  • University of Novi Sad, Faculty of Sport and Physical Education
    Novi Sad, 21000, Serbia
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

2 registry updates since Sep 25, 2026
Eligibility
Maximum age 12 Years→11 Years; 1 inclusion criterion edited
What changed in the criteria
Inclusion criteria
  • EditedNo other medical conditionscurrent acute illness, including Coronavirus Disease 2019 (COVID-19)
Oct 26, 2026
Interventions
Added Multisport (CON) Group. Arm changed Control (CON) group→Multisport (CON) Group
Oct 26, 2026
Primary outcomes
10 edited
What changed in the outcomes
  • EditedShoulder displacement (ShD)Time frame: Baseline and post-intervention (9 months)
  • EditedShoulder rotation (ShR)Time frame: Baseline and post-intervention (9 months)
  • EditedPelvic rotation (PeR)Time frame: Baseline and post-intervention (9 months)
  • EditedPelvic displacement (PeD)Time frame: Baseline and post-intervention (9 months)
  • EditedSagittal distance cervical spine-sacrum (Dcess)Time frame: Baseline and post-intervention (9 months)
  • EditedSagittal distance thoracic spine-sacrum (Dthsc)Time frame: Baseline and post-intervention (9 months)
  • EditedSagittal distance lumbar spine-sacrum (Dluss)Time frame: Baseline and post-intervention (9 months)
  • EditedFrontal cervical spine (CeS)Time frame: Baseline and post-intervention (9 months)
  • EditedFrontal thoracic spine (ThS)Time frame: Baseline and post-intervention (9 months)
  • EditedFrontal lumbar spine (LuS)Time frame: Baseline and post-intervention (9 months)
Oct 26, 2026
Secondary outcomes
2 description edited
What changed in the outcomes
  • DescriptionBody height: how it is measured was reworded
  • DescriptionBody mass: how it is measured was reworded
Oct 26, 2026
Registered
First appeared on the registry
Oct 21, 2026
Show all 2 updates
  1. Oct 26, 2026
    Eligibility Maximum age 12 Years→11 Years; 1 inclusion criterion edited
    What changed in the criteria
    Inclusion criteria
    • EditedNo other medical conditionscurrent acute illness, including Coronavirus Disease 2019 (COVID-19)
    Primary outcomes 10 edited
    What changed in the outcomes
    • EditedShoulder displacement (ShD)Time frame: Baseline and post-intervention (9 months)
    • EditedShoulder rotation (ShR)Time frame: Baseline and post-intervention (9 months)
    • EditedPelvic rotation (PeR)Time frame: Baseline and post-intervention (9 months)
    • EditedPelvic displacement (PeD)Time frame: Baseline and post-intervention (9 months)
    • EditedSagittal distance cervical spine-sacrum (Dcess)Time frame: Baseline and post-intervention (9 months)
    • EditedSagittal distance thoracic spine-sacrum (Dthsc)Time frame: Baseline and post-intervention (9 months)
    • EditedSagittal distance lumbar spine-sacrum (Dluss)Time frame: Baseline and post-intervention (9 months)
    • EditedFrontal cervical spine (CeS)Time frame: Baseline and post-intervention (9 months)
    • EditedFrontal thoracic spine (ThS)Time frame: Baseline and post-intervention (9 months)
    • EditedFrontal lumbar spine (LuS)Time frame: Baseline and post-intervention (9 months)
    Secondary outcomes 2 description edited
    What changed in the outcomes
    • DescriptionBody height: how it is measured was reworded
    • DescriptionBody mass: how it is measured was reworded
    Interventions Added Multisport (CON) Group. Arm changed Control (CON) group→Multisport (CON) Group
    + 3 other changes: index terms, description and conditions
  2. Oct 21, 2026
    First appeared on the registry

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
NCT07886749
Lead sponsor
University of Novi Sad
Responsible party
Dragan Marinkovic (Lead Investigator, University of Novi Sad) — Principal investigator
First posted
Oct 21, 2026
Start date
Sep 1, 2021
Primary completion
Jun 4, 2022
Completion
Jun 4, 2022
Last update
Oct 26, 2026

Oversight

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

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