Malnutrition and Sarcopenia Among Primary Ciliary Dyskinesia

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age6-18
SponsorIzmir Democracy University

About this trial

The prevalence and causes of malnutrition and sarcopenia in children and adolescents with Primary ciliary dyskinesia (PCD) have not been sufficiently elucidated. The aim of this study is to investigate the prevalence of malnutrition and sarcopenia in children and adolescents with PCD.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Unexplained neonatal respiratory distress, lateralization defect, productive cough, bronchiectasis, daily nasal congestion, and pansinusitis, as well as laboratory tests such as high-speed video microscopy, transmission electron microscopy, or genetic testing according to the European Respiratory Society diagnostic guidelines.

Cooperative individuals,

Individuals who have never smoked

Willingness to participate in the study

Disqualifiers

Individuals with any acute, chronic, or systemic illness other than PCD

Individuals who smoke or are quitting smoking

Individuals who are not willing to participate in the study

Individuals who are uncooperative

Trial population

The study will include children and adolescents aged 6-18 years with Primary Ciliary Dyskinesia (PCD).

Trial design

Design model

Case-only

Time perspective

Cross-sectional

Treatments tested in this trial

  • Physical assessments of individuals

    Other intervention

    Participants will be evaluated in terms of nutritional status, anthropometric measurements (waist circumference, hip circumference, waist-to-height ratio, skinfold measurements) and body composition, pulmonary functions, anaerobic capacity, muscle strength.

Treatment groups

15 Participants
are divided into 1 treatment group
Group A: Patient of Primary Ciliary Dyskinesia1 intervention

Trial outcomes

Primary outcomes

1

Handgrip Muscle Strength in Participants

Bilateral grip strength in children and adolescents with PCD will be measured in kgF using a hand dynamometer.

Time frame
From enrollment to the end of treatment at 1 year

Secondary outcomes

1

Malnutrition risk score in Participants

The Nutritional Status and Growth Risk Screening Tool will be used to assess the risk of growth failure. The total score on this scale ranges from 0 to 5; a score of 0 indicates a low risk of malnutrition, a score of 1-3 indicates a moderate risk of malnutrition, and a score of 4-5 indicates a high risk of malnutrition.

Time frame
From enrollment to the end of treatment at 1 year
2

Body Weight

Body weight in children and adolescents with PCD will be measured using a pediatric scale.

Time frame
From enrollment to the end of treatment at 1 year
3

Height

In children and adolescents with PCD, height will be measured using a stadiometer.

Time frame
From enrollment to the end of treatment at 1 year
4

Body Mass Index

For children and adolescents with PCD, the body mass index will be calculated by dividing body weight by the square of height in meters.

Time frame
From enrollment to the end of treatment at 1 year

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: