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Breathing battle: which device helps CP Kids' lungs after COVID?

NCT ID NCT07508332

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested two breathing devices—a Lung Boost trainer and an incentive spirometer—to see which better improves lung function in 60 children aged 4-9 with cerebral palsy who had recovered from COVID-19. All children also received standard breathing therapy. The goal was to find a fun, motivating way to help these kids breathe easier and improve their quality of life.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

60 people

The number who actually took part.

Started

Jul 2023

Finished

Jan 2024

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

4 to 9 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. 60 patients from both genders. 2. spastic CP patients between the ages 4 and 9 years. 3. Reasonable cognitive functions and a reasonable IQ so as to be able to follow instructions. 4. after two weeks of COVID19 recovery Exclusion Criteria: 1. Had other psychiatric and/or neurological disorders than cerebral palsy as Seizures. 2. Had any spinal deformities that affect chest mobility or pulmonary functions 3. Had medical conditions that could affect respiratory function such as cardiac disease or Chronic respiratory disease or on medications that affect respiratory function

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Amira Galal Mahmoud

    Cairo, Heliopolis, 11757, Egypt

  • Doaa Adel Abdel Aziz

    Cairo, Heliopolis, 11757, Egypt

  • Faten Mohamed Hassan

    Cairo, Heliopolis, 11757, Egypt

  • Mai Abdelghani Eid

    Cairo, Heliopolis, 11757, Egypt

  • Mai Magdy Ahmed

    Cairo, Heliopolis, 11757, Egypt

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