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Animation-Based Breathing Therapy for School-Age Children

I

Istanbul University - Cerrahpasa

Status

Invitation-only

Conditions

Children
Breathing Patterns
School Health
Stress

Treatments

Other: Animation-based breathing therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT06988254
17052025

Details and patient eligibility

About

This randomized controlled trial aims to investigate the efficacy of animation-based breathing therapy on the physical (cough strength, chest expansion, and walking speed) and psychological health (perceived stress level, well-being, and attention) of school-age children.

Full description

One hundred thirty school-age children, aged between 8 and 12, will be randomly assigned to one of two groups: an animation-based breathing therapy group or a control group. The intervention group will receive animation-based breathing therapy for six weeks (two sessions per day, five days per week). Assessments will be conducted at baseline and at the end of the six-week period. Cough strength will be measured using a peak expiratory flow meter. Chest expansion will be assessed with a measuring tape at the axillary, epigastric, and subcostal levels. Walking speed will be evaluated using the 10-Meter Walk Test. Perceived stress will be assessed using the Perceived Stress Scale for Children, well-being will be measured using the WHO-5 Child Wellbeing Index, and attention will be assessed using the Bourdon Attention Test.

Enrollment

130 estimated patients

Sex

All

Ages

8 to 12 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

-- Children aged between 8 and 12 years,

  • Attending school and formal education regularly,
  • Volunteers whose parents and themselves agreed to participate after being informed about the purpose of the study and the procedures involved, and who provided written informed consent.

Exclusion criteria

  • Children with any condition that may prevent them from completing self-reported questionnaires during the assessment (e.g., difficulty in understanding forms, physical disabilities, illiteracy),
  • History of any upper or lower extremity injury within the past six months,
  • History of any upper or lower extremity surgery within the past six months,
  • Presence of any soft tissue disorder,
  • Diagnosed with serious gastrointestinal, cardiovascular, pulmonary, or hematological disorders following examination by a specialist physician,
  • Diagnosed spinal problems such as scoliosis, kyphosis, or kyphoscoliosis,
  • Diagnosed with psychotic disorder, bipolar disorder, or autism spectrum disorder,
  • History of epilepsy or serious head trauma,
  • Current use of psychotropic medications.

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

130 participants in 2 patient groups

Animation-based breathing therapy
Experimental group
Description:
The intervention includes the animation-based breathing therapy for six weeks (two sessions per day, five days per week).
Treatment:
Other: Animation-based breathing therapy
Control
No Intervention group
Description:
No Intervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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