Pediatric Nursing EducationNCT07446920
"Effect of Artificial Intelligence-Driven Mobile Application on Nurses' Knowledge and Attitudes Toward Atraumatic Care for Hospitalized Children"
A study testing Atraumatic Care Training Program in people with Pediatric Nursing Education, run by University of Baghdad at 1 site in Iraq.
Trial summary
This randomized controlled trial aims to evaluate the effect of an artificial intelligence-driven mobile application on nurses' knowledge and attitudes toward atraumatic care for hospitalized children. Read more about this study
- Who is it for?
- Ages 18 to 50 yearsHealthy volunteers can take part
- Conditions the study is for
- Pediatric Nursing Education
- What is being tested?
- Atraumatic Care Training Program
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 97 participants
- Where
- 1 siteIraq
- Study dates
- 29 Dec 2025to 2 Feb 2026
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 50 years
- All sexes
- Healthy volunteers accepted
- Adult
Who may be able to join
- The study included nurses who:
- Work in the participating units and provide direct nursing care to children or neonates.
- Own a smartphone and are capable of using it (as the intervention is delivered via a mobile application).
- Agree to participate and provide written informed consent
Who cannot join
- Nurses were excluded if they:
- Perform only administrative tasks (e.g., statistics/records) without providing direct patient care.
- Are expected to take long-term leave during the intervention/follow-up period
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Effect of Artificial Intelligence-Driven Mobile Application on Nurses' Knowledge and Attitude Toward Atraumatic Care for Hospitalized Children: A Randomized Controlled Trial
This randomized controlled trial aims to evaluate the effect of an artificial intelligence-driven mobile application on nurses' knowledge and attitudes toward atraumatic care for hospitalized children. Participants, who are pediatric nurses, will be randomly assigned to either the intervention group, using the mobile application, or the control group receiving standard education. The primary outcomes are improvements in nurses' knowledge and attitudes, measured after the intervention. The study seeks to determine whether the mobile application enhances nurses' competence in providing atraumatic care compared to usual training methods.
Read the detailed description
This randomized controlled trial investigates the effectiveness of an artificial intelligence-driven mobile application designed to enhance nurses' knowledge and attitudes toward atraumatic care for hospitalized children. Pediatric nurses working in hospital units will be randomly assigned to either the intervention group, which will use the mobile application, or the control group, which will receive standard education. The intervention aims to provide interactive learning modules, case scenarios, and practical guidelines for atraumatic care. Primary outcomes include improvements in knowledge scores and attitude assessments, measured before and after the intervention. Secondary outcomes include participants' satisfaction with the application and self-reported confidence in providing atraumatic care. The study is expected to provide evidence on the utility of mobile AI-based educational tools in improving nursing competence and patient care in pediatric settings.
- Conditions
- Pediatric Nursing Education
- Being tested
- Atraumatic Care Training Program, No Intervention / Standard Care
- Keywords
- Atraumatic Care, Pediatric Nursing, Hospitalized Children, Nursing Education, AI, Mobile Application, RCT
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Atraumatic Care Training ProgramBehavioural
The intervention consisted of an AI-driven mobile application designed to enhance nurses' knowledge and attitudes toward atraumatic care for hospitalized children. The application included educational modules covering principles, benefits, and purposes of atraumatic care. Each module provided AI-generated content and an interactive chat feature, requiring participants to ask at least three questions before unlocking a module-specific quiz. Participants completed all modules over one week, followed by a final assessment of 25 AI-generated questions covering all modules
No Intervention / Standard CareBehavioural
Nurses in this group will continue their routine practice without receiving any additional training, mobile application, or educational program. Participants will provide pediatric care according to standard hospital protocols. This group serves as a comparison to evaluate the effect of the AI-driven mobile application on the experimental group.
| Study group | Role | What they receive |
|---|---|---|
| Nurses Receiving Atraumatic Care Training" | Experimental | Participants receive the AI-driven mobile application containing educational modules on atraumatic care, an interactive AI-based chat for at least three questions per module, module quizzes of 10 AI-generated questions, and a final assessment of 25 questions covering all modules. Completion of each module and quiz is required to advance Receives: Behavioral: Atraumatic Care Training Program |
| Control group | Other | Nurses in this group will continue their routine practice without receiving any additional training, mobile application, or educational program. This group serves as a comparison to evaluate the effect of the AI-driven mobile application on the experimental group. Participants follow standard hospital protocols and provide care as usual, without exposure to the study intervention. Receives: Behavioral: No Intervention / Standard Care |
What is being measured
The primary outcome is the main question the study is designed to answer.
Nurses' Knowledge about Atraumatic Care
Change in nurses' knowledge scores regarding atraumatic care for hospitalized children, measured using a validated knowledge questionnaire administered before and after the AI-driven mobile application intervention.
Measured: Pre-test and immediately post-intervention (after completing the mobile application modules).
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted3 Mar 2026
- Study start29 Dec 2025
- Primary completion2 Feb 2026
- Study completion2 Feb 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Pediatric Nursing EducationStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Participants were randomly assigned to either the intervention group receiving the AI-driven mobile application or the control group receiving usual care.
- Masking
- None (open label)
- Enrolment
- 97 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Baghdad
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Mustafa Sahib Ali, University of Baghdad
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07446920
- Sponsor's protocol ID
- 2025-11-09
- Status last verified
- Feb 2026
- First submitted
- 25 Feb 2026
- Last updated
- 3 Mar 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 3 Mar 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effect of Artificial Intelligence-Driven Mobile Application on Nurses' Knowledge and Attitude Toward Atraumatic Care for Hospitalized Children: A Randomized Controlled Trial
- ClinicalTrials.gov ID
- NCT07446920
- Acronym / sponsor ID
- 2025-11-09
- Conditions
- Pediatric Nursing Education
- Keywords
- Atraumatic Care, Pediatric Nursing, Hospitalized Children, Nursing Education, AI, Mobile Application, RCT
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 97 participants (actual)
- Lead sponsor
- University of BaghdadUniversity, hospital or other
- Study start
- 29 Dec 2025 (actual)
- Primary completion
- 2 Feb 2026 (actual)
- Study completion
- 2 Feb 2026 (actual)
- First posted
- 3 Mar 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This randomized controlled trial aims to evaluate the effect of an artificial intelligence-driven mobile application on nurses' knowledge and attitudes toward atraumatic care for hospitalized children. Participants, who are pediatric nurses, will be randomly assigned to either the intervention group, using the mobile application, or the control group receiving standard education. The primary outcomes are improvements in nurses' knowledge and attitudes, measured after the intervention. The study seeks to determine whether the mobile application enhances nurses' competence in providing atraumatic care compared to usual training methods.
Detailed description
This randomized controlled trial investigates the effectiveness of an artificial intelligence-driven mobile application designed to enhance nurses' knowledge and attitudes toward atraumatic care for hospitalized children. Pediatric nurses working in hospital units will be randomly assigned to either the intervention group, which will use the mobile application, or the control group, which will receive standard education. The intervention aims to provide interactive learning modules, case scenarios, and practical guidelines for atraumatic care. Primary outcomes include improvements in knowledge scores and attitude assessments, measured before and after the intervention. Secondary outcomes include participants' satisfaction with the application and self-reported confidence in providing atraumatic care. The study is expected to provide evidence on the utility of mobile AI-based educational tools in improving nursing competence and patient care in pediatric settings.
Study design
- Primary purpose
- Other
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- Participants were randomly assigned to either the intervention group receiving the AI-driven mobile application or the control group receiving usual care.
| Arm | Type | Receives |
|---|---|---|
| Nurses Receiving Atraumatic Care Training" | Experimental | Behavioral: Atraumatic Care Training ProgramParticipants receive the AI-driven mobile application containing educational modules on atraumatic care, an interactive AI-based chat for at least three questions per module, module quizzes of 10 AI-generated questions, and a final assessment of 25 questions covering all modules. Completion of each module and quiz is required to advance |
| Control group | Other | Behavioral: No Intervention / Standard CareNurses in this group will continue their routine practice without receiving any additional training, mobile application, or educational program. This group serves as a comparison to evaluate the effect of the AI-driven mobile application on the experimental group. Participants follow standard hospital protocols and provide care as usual, without exposure to the study intervention. |
Who may qualify
- Ages
- 18 to 50 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (4 listed)
- The study included nurses who:
- Work in the participating units and provide direct nursing care to children or neonates.
- Own a smartphone and are capable of using it (as the intervention is delivered via a mobile application).
- Agree to participate and provide written informed consent
Key exclusion criteria (3 listed)
- Nurses were excluded if they:
- Perform only administrative tasks (e.g., statistics/records) without providing direct patient care.
- Are expected to take long-term leave during the intervention/follow-up period
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Atraumatic Care Training ProgramThe intervention consisted of an AI-driven mobile application designed to enhance nurses' knowledge and attitudes toward atraumatic care for hospitalized children. The application included educational modules covering principles, benefits, and purposes of atraumatic care. Each module provided AI-generated content and an interactive chat feature, requiring participants to ask at least three questions before unlocking a module-specific quiz. Participants completed all modules over one week, followed by a final assessment of 25 AI-generated questions covering all modules | Behavioural | Nurses Receiving Atraumatic Care Training" |
| No Intervention / Standard CareNurses in this group will continue their routine practice without receiving any additional training, mobile application, or educational program. Participants will provide pediatric care according to standard hospital protocols. This group serves as a comparison to evaluate the effect of the AI-driven mobile application on the experimental group. | Behavioural | Control group |
Primary outcome
Nurses' Knowledge about Atraumatic Care
Time frame: Pre-test and immediately post-intervention (after completing the mobile application modules).
Change in nurses' knowledge scores regarding atraumatic care for hospitalized children, measured using a validated knowledge questionnaire administered before and after the AI-driven mobile application intervention.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 3 Mar 2026.
- Individual participant dataSharing planned: No
Related trials for Pediatric Nursing Education
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Forensic Nursing Education in Pediatric Nurses, Forensic Competency Training
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Atraumatic Care Training Program in people with Pediatric Nursing Education, run by University of Baghdad at 1 site in Iraq.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 3 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Iraq. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Nurses' Knowledge about Atraumatic Care (time frame: Pre-test and immediately post-intervention (after completing the mobile application modules).). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Mar 2026; AzTrials last refreshed its copy on 28 Oct 2026.