ClinicalTrials.gg
Not yet recruitingNCT07230093Updated Nov 17, 2025

Exercise and Physical Fitness in Children With Specific Learning Disabilities

An interventional study of Combined Exercise Program in Learning Disabilities, sponsored by Bartın Unıversity. Not yet recruiting at 1 site in Turkey (Türkiye). Open to participants aged 7 Years to 14 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-11-17.

Sponsored by Bartın Unıversity · Not applicable, Interventional, and Other

From the registry’s dates

  • Primary completion was expected by Jan 2026, 9 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
18
Allocation
Non-randomized
Ages
7 Years to 14 Years
Sex
All
01

Study summary

Specific learning disabilities (SLD) are characterized by difficulties in reading, comprehension, arithmetic, and written expression, often accompanied by impairments in motor skills, balance, and coordination. However, physical difficulties in children with SLD are often overlooked in educational settings, and parental awareness of these issues remains limited.

This study aims to examine the effect of an 8-week combined exercise program-including balance, strength, and stretching exercises-on the physical fitness of children aged 7-14 years with SLD. Participants will be randomly assigned to either an exercise group or a control group.

The exercise intervention will be conducted three times per week for 45 minutes per session over eight weeks. Physical fitness will be evaluated through standardized field-based measures of balance, strength, flexibility, and endurance before and after the intervention. Data will be analyzed using SPSS 26.0, employing Wilcoxon, Mann-Whitney U, independent t-test, and paired t-test as appropriate.

The study is expected to emphasize the importance of physical activity for children with SLD and promote the inclusion of physiotherapy-based exercise programs in individualized support plans.

Primary Outcome Question: Does an 8-week combined exercise program improve balance, strength, flexibility, and endurance-key components of physical fitness-in children with specific learning disabilities compared to a control group?

Read the detailed description

The term "Learning Disability" refers to difficulties in achieving expected academic performance in specific areas despite normal intelligence. In Turkey, learning disabilities encompass difficulties in one or more cognitive processes necessary for understanding and using language, either written or spoken. These difficulties may manifest in listening, speaking, reading, writing, spelling, attention, or mathematical operations.

Children with Specific Learning Disabilities (SLD) often experience not only academic difficulties but also deficits in motor skills, balance, and coordination. Physical fitness, defined as the ability to perform daily activities efficiently and safely, depends on multiple parameters including flexibility, muscular strength, muscular endurance, balance, coordination, speed, and agility. Regular exercise can improve these parameters, supporting children's physical, social, and cognitive development.

Despite the importance of physical fitness, studies on exercise interventions in SLD children are limited and mostly focus on balance. There is a lack of research investigating comprehensive combined exercise programs addressing multiple fitness components simultaneously.

The aim of this study is to examine the effects of a combined exercise program on physical fitness parameters in children with SLD aged 7-14 years. The primary objectives are:

To improve flexibility, muscular strength, muscular endurance, balance, coordination, speed, and agility.

To prevent deficits in gross and fine motor skills commonly observed in children with SLD.

To increase parental awareness of the importance of physical exercise in children with learning disabilities.

To provide a home-based exercise guide for children and parents to promote sustainable physical activity.

This randomized controlled study will be conducted in Bartın, Turkey, with 18 participants diagnosed with SLD according to official assessments. Participants will be randomly assigned to the exercise group, which will receive the combined exercise program, or to the control group, which will not receive intervention. Physical fitness parameters will be measured before and after the intervention to evaluate changes.

The combined exercise program consists of 8 weeks of progressive training, three times per week, 45 minutes per session, including warm-up, main exercise, and cool-down phases. Exercises target all major muscle groups and incorporate strength, flexibility, balance, coordination, speed, and agility components.

Hypothesis: H0: "Combined exercise training has a significant positive effect on the physical fitness parameters of children with SLD." The novelty of this study lies in addressing physical fitness comprehensively in SLD children, beyond academic interventions, and promoting sustainable exercise habits. Results are expected to contribute to both the scientific literature and practical guidance for education and rehabilitation programs for children with learning disabilities.

02

Conditions studied

  • Learning Disabilities

Browse trials for

Keywords

  • Learning Disability
  • Physical Fitness
  • Combined Exercise
  • Children
  • Exercise Intervention
03

In context

Learning Disabilities

270 studies on the registry are indexed under Learning Disabilities; 62 are open to participants now.

This study's planned enrollment of 18 is below the median of 60 across 181 interventional studies indexed under Learning Disabilities.

Browse Learning Disabilities studies →

Lead sponsor

Bartın Unıversity is the lead sponsor of 47 studies on the registry; 11 are open to participants now.

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

04

Who can participate

Ages eligible
7 Years to 14 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

  • Exercise Group: Children aged 7-14 years diagnosed with Specific Learning Difficulty (SLD), with signed parental consent and child assent form
  • Control Group: Children aged 7-14 years without SLD (healthy), with signed parental consent and child assent form

Exclusion criteria

Exclusion Criteria:

  • Children with physical disabilities preventing participation
  • Children unable to cooperate with the assessments
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
18 participants (estimated)

Study arms

  • Experimental
    Exercise Group

    Participants receive a combined exercise program for 8 weeks, 3 days per week, 45 minutes per session. Physical fitness parameters-including flexibility, muscular strength, muscular endurance, balance, coordination, speed, and agility-are assessed before and after the intervention.

    Behavioral: Combined Exercise Program

  • No intervention
    Control Group

    Participants do not receive any intervention. Physical fitness parameters-including flexibility, muscular strength, muscular endurance, balance, coordination, speed, and agility-are assessed at the same time points as the exercise group.

Interventions

  • BehavioralCombined Exercise Program

    Participants perform a combined exercise program for 8 weeks, 3 days per week, 45 minutes per session. Physical fitness parameters-including flexibility, muscular strength, muscular endurance, balance, coordination, speed, and agility-are assessed before and after the intervention. This program aims to improve gross and fine motor skills, balance, coordination, and overall physical fitness in children with specific learning difficulties.

06

What researchers measure

Primary outcomes

  1. Balance Performance (Flamingo Balance Test)

    Description: Static balance will be assessed using the Flamingo Balance Test from the Eurofit Test Battery. Participants will stand on one leg on a narrow beam, and the number of falls within 1 minute will be recorded. Time Frame: Baseline and 8 weeks Unit of Measure: Number of falls (count) Interpretation: Lower scores indicate better balance.

    Time frame: Pre- and post-intervention (8 weeks)

  2. Coordination Speed (Plate Tapping Test)

    Description: Coordination and movement speed will be assessed using the Plate Tapping Test from the Eurofit Test Battery. The time required to complete 25 cycles of alternating taps will be recorded. Time Frame: Baseline and 8 weeks Unit of Measure: Seconds Interpretation: Lower scores indicate better performance.

    Time frame: Before and after intervention (8 weeks)

  3. Flexibility (Sit-and-Reach Test)

    Description: Flexibility will be measured using the Sit and Reach Test, which assesses hamstring and lower back flexibility. Time Frame: Baseline and 8 weeks Unit of Measure: Centimeters Interpretation: Higher scores indicate greater flexibility.

    Time frame: Before and after intervention (8 weeks)

  4. Abdominal Muscle Endurance (Sit-Ups Test)

    Description: Abdominal muscle endurance will be assessed using the Sit-Ups Test, recording the number of repetitions completed in 30 seconds. Time Frame: Baseline and 8 weeks Unit of Measure: Number of sit-ups (count) Interpretation: Higher scores indicate better endurance.

    Time frame: Before and after intervention (8 weeks)

  5. Lower Limb Power (Standing Long Jump Test)

    Description: Explosive leg power will be evaluated using the Standing Long Jump Test. The best distance achieved in three trials will be recorded. Time Frame: Baseline and 8 weeks Unit of Measure: Centimeters Interpretation: Higher scores indicate better performance.

    Time frame: Before and after intervention (8 weeks)

  6. Cardiorespiratory Endurance (20 m Shuttle Run Test)

    Description: Aerobic endurance will be assessed using the 20-meter Shuttle Run Test (Eurofit). The number of completed stages will be recorded. Time Frame: Baseline and 8 weeks Unit of Measure: Number of completed stages Interpretation: Higher scores indicate better endurance.

    Time frame: Before and after intervention (8 weeks)

  7. Age

    Measurement: Years Description: Chronological age of the participant will be recorded. Time Frame: Baseline (Pre-intervention)

    Time frame: Baseline (Pre-intervention)

  8. Sex

    Measurement: Male / Female (categorical variable) Description: Biological sex will be recorded to explore potential differences in physical fitness outcomes. Time Frame: Baseline (Pre-intervention)

    Time frame: Baseline (Pre-intervention)

  9. Body Mass Index (BMI)

    Measurement: kg/m² Description: BMI will be calculated using measured body weight and height (BMI = weight \[kg\] / height² \[m²\]). It will be used as a descriptive and covariate variable in analysis. Interpretation: Higher or lower BMI values will be examined in relation to physical fitness outcomes. Time Frame: Baseline (Pre-intervention)

    Time frame: Baseline (Pre-intervention)

07

Study locations

1 site
  • Bartın University, Vocational School of Health Services
    Bartın, Bartın 74100, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Nov 2025; primary completion for Jan 2026, 2 months later.

Of 96 non-industry interventional studies with no phase under Learning Disabilities, half reached primary completion within 30 months of starting (the median), counting those still running; a quarter within 9 and three quarters within 53. This study's planned 2 months is below that.

Counting every sponsor, half of 99 studies reached it within 29 months; a quarter within 9 and three quarters within 51.

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

Registered
Sep 27, 2025
First posted
Nov 17, 2025
StartEst.
Nov 25, 2025
Primary completionEst.
Jan 30, 2026
CompletionEst.
Feb 15, 2026
Last update
Nov 17, 2025
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.
No changes since tracking began. The registry record was last updated on Nov 17, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07230093
Lead sponsor
Bartın Unıversity
Responsible party
Meryem Sevim (PT, PhD, Lecturer, Department of Physiotherapy, Bartın Unıversity) — Principal investigator
First posted
Nov 17, 2025
Start date
Nov 25, 2025 (estimated)
Primary completion
Jan 30, 2026 (estimated)
Completion
Feb 15, 2026 (estimated)
Last update
Nov 17, 2025

Study contacts

Meryem Sevim, PhD
Contact
fzt.meryemsevim@outlook.com
+905536104510

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 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion