NCT07230093

Brief 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?

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
18

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Nov 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 27, 2025

Completed
2 months until next milestone

First Posted

Study publicly available on registry

November 17, 2025

Completed
8 days until next milestone

Study Start

First participant enrolled

November 25, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 30, 2026

Completed
16 days until next milestone

Study Completion

Last participant's last visit for all outcomes

February 15, 2026

Completed
Last Updated

November 17, 2025

Status Verified

November 1, 2025

Enrollment Period

2 months

First QC Date

September 27, 2025

Last Update Submit

November 13, 2025

Conditions

Keywords

Learning DisabilityPhysical FitnessCombined ExerciseChildrenExercise Intervention

Outcome Measures

Primary Outcomes (9)

  • 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.

    Pre- and post-intervention (8 weeks)

  • 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.

    Before and after intervention (8 weeks)

  • 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.

    Before and after intervention (8 weeks)

  • 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.

    Before and after intervention (8 weeks)

  • 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.

    Before and after intervention (8 weeks)

  • 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.

    Before and after intervention (8 weeks)

  • Age

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

    Baseline (Pre-intervention)

  • 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)

    Baseline (Pre-intervention)

  • 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)

    Baseline (Pre-intervention)

Study Arms (2)

Exercise Group

EXPERIMENTAL

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

Control Group

NO INTERVENTION

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

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.

Exercise Group

Eligibility Criteria

Age7 Years - 14 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17)

You may qualify if:

  • 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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Bartın University, Vocational School of Health Services

Bartın, Bartın, 74100, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Learning Disabilities

Condition Hierarchy (Ancestors)

Communication DisordersNeurobehavioral ManifestationsNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and SymptomsNeurodevelopmental DisordersMental Disorders

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Masking Details
No masking is applied in this study; participants, caregivers, and investigators are aware of group assignments.
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: Participants are assigned to one of two groups: the exercise group receives a combined exercise program for 8 weeks, 3 days per week, 45 minutes per session. The control group does not receive any intervention. Assessments of physical fitness parameters-including flexibility, muscular strength, muscular endurance, balance, coordination, speed, and agility-are performed before and after the intervention to evaluate changes.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PT, PhD, Lecturer, Department of Physiotherapy

Study Record Dates

First Submitted

September 27, 2025

First Posted

November 17, 2025

Study Start

November 25, 2025

Primary Completion

January 30, 2026

Study Completion

February 15, 2026

Last Updated

November 17, 2025

Record last verified: 2025-11

Data Sharing

IPD Sharing
Will not share

Locations