Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Infant Conditions
  • Respiratory Insufficiency
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: Comparison of tree parallel groups, 1 control and 2 intervention groups.Masking: Single (Investigator)Masking Description: Randomisation is carried out with sealed envelopes that are only opened just before intervention starts. There are different care givers who carry out the observations and who perform the interventions.Primary Purpose: Treatment

Participation Requirements

Age
Younger than 24 years
Gender
Both males and females

Description

All children under 2 years of age who are admitted to the hospital for respiratory distress and who have previously been essentially healthy are asked to participate. The infants will be randomized to 3 groups, 1 control group and 2 intervention groups. The infants in the control group will receive ...

All children under 2 years of age who are admitted to the hospital for respiratory distress and who have previously been essentially healthy are asked to participate. The infants will be randomized to 3 groups, 1 control group and 2 intervention groups. The infants in the control group will receive the standard care at the clinic. In one intervention group the parents will receive instructions how to vary their child body position regularly, and in the other intervention group the child will receive physiotherapy regularly and the parents will carry out some treatment. Further actions in the form of inhalations or stimulation of deep breathing, will be used when needed. The children will be observed following a structured observational protocol regularly throughout the hospital stay.

Tracking Information

NCT #
NCT03575091
Collaborators
Not Provided
Investigators
Principal Investigator: Eva Ekvall Hansson, PhD Lund University