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Clinical Trials/NCT07376863
NCT07376863CompletedNot Applicable

Effects of Gince Zumba and Square Stepping Exercises on Motor and Cognitive Functions in Children With Attention-Deficit/Hyperactivity Disorder

Cukurova University1 site in 1 country51 target enrollmentStarted: February 12, 2024Last updated:
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
51
Locations
1
Primary Endpoint
Stroop Color Test Completion Time

Study Overview

Brief Summary

The purpose of this study is to investigate the effects of structured exercise interventions (Gince Zumba and Square Stepping) on cognitive, motor and behavioral functions of children diagnosed with Attention Deficit Hyperactivity Disorder (ADHD). Specifically, this study aims to:

  • compare the effects of Gince Zumba and Square Stepping on motor perfoemance, including coordination and reaction time.
  • examine changes in cognitive functions, particularly attention and memory functions following each exercise intervention.
  • evaluate the impact of both exercise programs on behavioral symptoms and social adaptation as reported by parents
  • determine whether rhytm-based exercise (Gince Zumba) or cognitively demanding stepping exercise (Square Stepping) is more effective in imroving functional outcomes in children with ADHD.

Based on these aims, the study was conducted as follows:

  • Eligible participants were randomly assigned to one of the three intervention groups ( square stepping group, gince zumba group, control group)
  • All participants underwent baseline assessments prior to the interventions
  • Participants in the intervention groups performed assigned activities for eight weeks, while the control group did not engage in regular physical activity during the same period.
  • Following the completion of the interventions, all participants underwent post-intervention assessments

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
Single (Outcomes Assessor)

Masking Description

This was a single-blind study in which outcome assessors were blinded to group allocation

Eligibility Criteria

Ages
8 Years to 12 Years (Child)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Ability to read and understand Turkish language
  • Use of psychostimulant medication for at least 2 months prior to enrollment

Exclusion Criteria

  • Diagnosis of intellectual disability
  • Comorbidity of medical or psychiatric
  • Inability to participate in physical activity

Arms & Interventions

Gince Zumba Group

Experimental

Participants in this arm received the Gince Zumba exercise program conducted two times per week for eight weeks

Intervention: Gince Zumba Exercise (Other)

Square Stepping Group

Experimental

Participants in this arm received the Square Stepping exercise program conducted two times per week for eight weeks

Intervention: Square Stepping Exercise (Other)

Control Group

No Intervention

Participants in this arm received no regular physical activity for eight weeks

Outcomes

Primary Outcomes

Stroop Color Test Completion Time

Time Frame: Baseline and at the end of the 8-week intervention

The Stroop Color Test is a neuropsychological assessment used to evaluate selective attention, cognitive flexibility, and inhibitory control. In this study, the primary outcome is the total time required to complete the interference condition of the Stroop task, measured in seconds. Shorter completion time indicates better attentional control and executive functioning. Measurements will be obtained before and after the 8-week exercise intervention.

Visual-Auditory Digit Span Test Total Score

Time Frame: Baseline and after 8 weeks

The Visual-Auditory Digit Span Test (VADST) is a neuropsychological assessment used to evaluate short-term memory and working memory through auditory and visual digit recall tasks. The primary outcome measure is the total test score, expressed in points, obtained from correct responses across all subtests. Higher total scores indicate better memory performance and cognitive processing capacity. The assessment will be administered at baseline and after the 8-week intervention period.

Secondary Outcomes

  • Blaze Pod Reaction Time Score(Baseline and after 8 weeks)
  • Blaze Pod Number of Hits(Baseline and after 8 weeks)
  • Blaze Pod Total Number of Errors(Baseline and after 8 weeks)
  • Conners Parent Rating Scale Total Score(Baseline and after 8 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Ceylan Ekerer

Principal Investigator

Cukurova University

Study Sites (1)

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