NCT07376863

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

Trial Health

87
On Track

Trial Health Score

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

Enrollment
51

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Feb 2024

Geographic Reach
1 country

1 active site

Status
completed

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

Study Start

First participant enrolled

February 12, 2024

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 15, 2025

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

May 29, 2025

Completed
7 months until next milestone

First Submitted

Initial submission to the registry

January 2, 2026

Completed
27 days until next milestone

First Posted

Study publicly available on registry

January 29, 2026

Completed
Last Updated

January 29, 2026

Status Verified

January 1, 2026

Enrollment Period

1.1 years

First QC Date

January 2, 2026

Last Update Submit

January 26, 2026

Conditions

Outcome Measures

Primary Outcomes (2)

  • Stroop Color Test Completion Time

    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.

    Baseline and at the end of the 8-week intervention

  • Visual-Auditory Digit Span Test Total Score

    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.

    Baseline and after 8 weeks

Secondary Outcomes (4)

  • 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

Study Arms (3)

Gince Zumba Group

EXPERIMENTAL

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

Other: Gince Zumba Exercise

Square Stepping Group

EXPERIMENTAL

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

Other: Square Stepping Exercise

Control Group

NO INTERVENTION

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

Interventions

The Gince Zumba interventions consisted of rhythm-based aerobic exercises , requiring cognitive engagement through attention, coordination, and sequencing of movements, and aiming to support cognitive functions."

Also known as: Gince Zumba Exercises
Gince Zumba Group

The Square Stepping Exercise intervention consisted of step patterns performed on a gridded mat in group sessions,, requiring cognitive engagement through visuospatial processing, attention, working memory, and sequencing of movement patterns, and aiming to support cognitive functions."

Square Stepping Group

Eligibility Criteria

Age8 Years - 12 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17)

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Cukurova University, Faculty of Medicine

Adana, 01170, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Attention Deficit Disorder with Hyperactivity

Condition Hierarchy (Ancestors)

Attention Deficit and Disruptive Behavior DisordersNeurodevelopmental DisordersMental Disorders

Study Officials

  • Gonca İnce, Prof.

    Cukurova University

    STUDY CHAIR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
This was a single-blind study in which outcome assessors were blinded to group allocation
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Model Details: There are 3 groups involved in the study. Each of two of the groups joined two different kinds of exercise interventions, and the control group didnt involve any regular physical activity.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

January 2, 2026

First Posted

January 29, 2026

Study Start

February 12, 2024

Primary Completion

March 15, 2025

Study Completion

May 29, 2025

Last Updated

January 29, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will share

De-identified individual participant data underlying the results reported in publications will be made available upon reasonable request to the corresponding author, subject to ethical approval and a data use agreement

Shared Documents
STUDY PROTOCOL
Time Frame
Beginning after publication of the primary results
Access Criteria
Data access will be provided upon reasonable request, subject to ethical approval and a data use agreement
More information

Locations