Tracheostomy-Related Swallowing Issues in Children.
Eileen M Raynor, Daniel Wohl
https://pubmed.ncbi.nlm.nih.gov/38508881/Actively Recruiting
Led by Karolinska Institutet · Updated on 2026-02-13
80
Participants Needed
2
Research Sites
N/A
Total Duration
Researchers are investigating the relationship between feeding difficulties and self-assessed quality of life in children with tracheal cannulas. This observational study focuses on children with tracheostomies, a surgical opening in the neck to aid breathing, who may experience challenges with feeding and lower quality of life. The study aims to understand the types of feeding difficulties these children face, how they and their caregivers perceive their quality of life, and whether feeding issues affect their well-being. The study will include children under 18 years old who have tracheostomies and are followed regularly at the Long-term Intensive Care Unit LIVA at Karolinska University Hospital. Quality of life will be measured using the PedsQL instrument, covering health, emotions, social functioning, and schooldaycare activities. Feeding difficulties will be assessed using The Montreal Childrens Hospital Feeding Scale, which evaluates feeding abilities and behaviors. These assessments will take place during routine multidisciplinary team visits. Participants will undergo evaluations lasting about 10 minutes each as part of their scheduled care visits. Researchers will compare the quality of life and feeding difficulty scores with data from other populations to explore associations. The main outcomes measured over two years include feeding difficulties and quality of life in children with tracheostomies. This study will help identify factors that affect quality of life in this group and is ethically approved with ongoing follow-up planned until March 2027.
CONDITIONS
Feeding Difficulties and Quality of Life in Children With Tracheal Cannula
I
Ida Engqvist Engqvist, Medical Doctor
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Karolinska Institutet
Lead Sponsor
Region Stockholm
Collaborating Sponsor
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You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 2 years
Participants who undergo routine care are observed during their regular follow-up visits at the Long-term Intensive Care Unit (LIVA). Feeding difficulties and quality of life assessments are conducted using questionnaires and feeding scales within the multidisciplinary team visits.
Regular multidisciplinary team visits during follow-up
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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Lead Sponsor
Region Stockholm
Collaborating Sponsor