Effect of Video Game-Based Lung Volume Increasing Training on Respiratory Mechanics in Children With Developmental Delays: Randomized Controlled Study
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Enrollment
- 18
- Locations
- 1
- Primary Endpoint
- FEV1/FVC Measurement
Study Overview
Brief Summary
The aim of the study was to investigate the effect of video game-based lung volume increasing training on respiratory mechanics in children with developmental delays. Individuals with special needs are people who, for various reasons, show significant awareness at the level expected from their peers in terms of their individual characteristics and educational qualifications. Individuals with special needs constitute an important part of our country. Children with special needs may have respiratory problems that may or may not be recognized because they are not diagnosed, as well as decreases in respiratory capacity. Decrease in lung volumes may be encountered in children with special needs with various diagnoses such as neuromuscular diseases, cerebral palsy, cystic fibrosis, autism, and Down syndrome.
Pulmonary rehabilitation is a multidisciplinary program that balances or reverses the physiopsychopathology of pulmonary disorders and tries to help the patient reach high functional capacity as much as his physical condition and pulmonary disability allow. Chest physiotherapy, which is an important step of pulmonary rehabilitation, is a rehabilitation intervention used to reduce airway resistance, improve gas exchange and facilitate breathing in children. Active video game systems produced with the development of new technologies are used for the positive progression of rehabilitation, especially in young individuals who are extensive users of digital devices. For children who need a pulmonary rehabilitation program, active video game systems are preferred in the clinic as they increase the compatibility of the sessions and ensure continuity.
Detailed Description
It seems that there are insufficient studies in the literature on the effects of exercises that increase lung capacity on children with special needs. To the best of our knowledge, there is no study investigating the effects of programs to increase lung volumes in children with special needs in a randomized controlled study design. With this project, we aimed to reveal the effects of a lung volume-increasing exercise program performed with a video-based game system applied for 6 weeks in children with special needs, by comparing it with the control group that received only conventional rehabilitation. The duration of the treatment program in our study is also one of our unique values. According to our literature research, the implementation of a lung capacity-increasing rehabilitation program in children with special needs in the form of supervision twice a week and a home program once a week for 6 weeks is the first.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Single (Participant)
Masking Description
Each children were be interviewed and evaluated alone.
Eligibility Criteria
- Ages
- 7 Years to 18 Years (Child, Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Volunteer of the family to participate in the study
- •Stable clinical status at inclusion without infection or exacerbation in the previous 4 weeks
- •Children who have not been included in another clinical trial within the last month
- •Participants with a Body Mass Index (BMI) below 30 kilograms/square meter
Exclusion Criteria
- •Those with severe comorbidities, unstable coronary artery disease, collagen vascular diseases, and those requiring high-flow oxygen therapy (3-4 L\min).
- •History of exertional syncope or any comorbidity that prevents exercise training
- •Inability to communicate with the child and the child not obeying commands in any way
- •Children with vision problems
Arms & Interventions
Study Group (SGr)
In addition to institutional conventional rehabilitation, this group included breathing exercises to increase lung volumes and a 21-minute breathing exercise with video-based biofeedback.
Intervention: Experimental: Study Group (SGr) (Other)
Control Group (CGr)
This group was given only institutional conventional rehabilitation.
Intervention: Sham Comparator: Control Group (CGr) (Other)
Outcomes
Primary Outcomes
FEV1/FVC Measurement
Time Frame: Change from baseline lungs volumes at 6 weeks.
Respiratory Function Test. The COSMED microQuark spirometer used. Lung volume was evaluated.
FEV1 Measurement
Time Frame: Change from baseline lungs volumes at 6 weeks.
Respiratory Function Test. The COSMED microQuark spirometer used. Lung volume was evaluated.
FVC Measurement
Time Frame: Change from baseline lungs volumes at 6 weeks.
Respiratory Function Test. The COSMED microQuark spirometer used. Lung volume was evaluated.
PEF Measurement
Time Frame: Change from baseline lungs volumes at 6 weeks.
Respiratory Function Test. The COSMED microQuark spirometer used. Positive airway flow rate was evaluated.
Secondary Outcomes
- Pulse measurement(Change from baseline lungs volumes at 6 weeks.)
- Saturation measurement(Change from baseline lungs volumes at 6 weeks.)