CompletedNot Applicable

Effect of Virtual Reality on Pain, Arterial Blood Gases and Functional Capacity in Children After Open Heart Surgery

Egypt40 participantsStarted 2024-08-10

Plain-language summary

This study will be conducted to investigate: * The effect of virtual reality on pain in children after open heart surgery, * The effect of virtual reality on arterial blood gases in children after open heart surgery, * The effect of virtual reality on functional capacity in children after open heart surgery.

Who can participate

Age range

6 Years – 12 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Both genders will be included. * Their age range from 6 to 12 years. * Children after open heart surgery ( phase I cardiac rehabilitation). Exclusion Criteria: The children have one or more of the following will be excluded: * Any child Suffering from any other chronic congenital diseases. * Severe visual or auditory problems. * Neurological problems. * Vertigo problems. * Post surgical hemorrhage. * Post surgical arrhythmia.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

pain level

Timeframe: 1 hour /session 1 time / day for 5 consecutive days

arterial blood gases

Timeframe: 1 hour /session 1 time / day for 5 consecutive days

functional capacity

Timeframe: 1 hour /session 1 time / day for 5 consecutive days

Trial details

NCT IDNCT06712368

SponsorCairo University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-01-10

View on ClinicalTrials.gov More Children After Open Heart Surgery trials

Plain-language summary

Who can participate

Age range

6 Years – 12 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.