Robot-Assisted Intervention for Recurrent Respiratory Infections in Preschoolers
NCT07930546, Not applicable, Completed, Xi'an Jiaotong University
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Robot-Assisted Intervention for Recurrent Respiratory Infections in Preschoolers | ClinicalTrials.gov |
| NCT number | NCT07930546 | ClinicalTrials.gov |
| Status | Completed | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 164 participants, actual | ClinicalTrials.gov |
| Lead sponsor | Xi'an Jiaotong University | ClinicalTrials.gov |
| Conditions | Recurrent Respiratory Tract Infections | ClinicalTrials.gov |
| Interventions | Robot-Assisted Ecological Momentary Intervention (RESPIRE) | ClinicalTrials.gov |
| First posted | 2026-11-12 | ClinicalTrials.gov |
| Last updated | 2026-11-12 | ClinicalTrials.gov |
Registered outcomes 8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Parental Health Literacy Score | Baseline (Week 0), Week 4, and Week 8 | Parental health literacy was assessed using a 33-item health literacy scale for parents of preschool children. The scale covers three dimensions: functional health literacy, interactive health literacy, and critical health literacy. The total health literacy score was assessed at three time points to evaluate changes throughout the eight-week intervention period. | ClinicalTrials.gov |
| Secondary | Number of Respiratory Tract Infection Episodes | Weeks 1-2, 3-4, 5-6, and 7-8 | The number of newly occurring respiratory tract infection episodes in each consecutive two-week observation period was determined using daily caregiver reports of children's respiratory symptoms. Respiratory infection episodes separated by seven days or fewer were counted as a single episode. Higher counts indicate more frequent respiratory tract infections. | ClinicalTrials.gov |
| Secondary | Proportion of Days With Respiratory Tract Infection Symptoms | Weeks 1-2, 3-4, 5-6, and 7-8 | The proportion of days with respiratory tract infection symptoms was calculated for each consecutive two-week observation period. The numerator was the number of days on which the child experienced respiratory tract infection symptoms, and the denominator was the total number of days with submitted health reports during the same period. The result was expressed as a percentage, with higher values indicating a greater burden of respiratory symptoms. | ClinicalTrials.gov |
| Secondary | Parenting Sense of Competence Scale Score | Baseline (Week 0), Week 4, and Week 8 | Parenting sense of competence was assessed using the 17-item Parenting Sense of Competence Scale (PSOC), which includes parenting efficacy and parenting satisfaction dimensions. Each item is rated on a six-point Likert scale, with reverse scoring applied to the parenting satisfaction items as specified in the study protocol. The possible total score ranges from 17 to 102, with higher scores indicating greater parenting sense of competence. | ClinicalTrials.gov |
| Secondary | Parenting Stress Index Short Form Score | Baseline (Week 0), Week 4, and Week 8 | Parenting stress was measured using the 15-item Parenting Stress Index Short Form (PSI-SF-15). The instrument includes three dimensions: parental distress, parent-child dysfunctional interaction, and difficult child. Each item is rated on a five-point Likert scale. The total score ranges from 15 to 75, with higher scores indicating greater parenting stress. | ClinicalTrials.gov |
| Other | Daily Electronic Health Diary Completion Rate | Daily throughout the 8-week intervention | The completion rate of daily electronic health diaries was calculated as the number of diary entries completed by caregivers divided by the number of scheduled diary entries during the eight-week intervention, multiplied by 100. Completion data were obtained from RESPIRE application logs. Higher percentages indicate better adherence to daily symptom reporting. | ClinicalTrials.gov |
| Other | System Usability Scale Score | Week 8 | System usability was assessed among intervention-group caregivers using the 10-item System Usability Scale (SUS). Each item was rated on a five-point scale. Item scores were adjusted for positive and negative wording, summed, and multiplied by 2.5 to obtain a total score ranging from 0 to 100. Higher scores indicate better perceived system usability. | ClinicalTrials.gov |
| Other | Percentage of Caregivers Satisfied With the RESPIRE Program | Week 8 | Intervention satisfaction was evaluated among caregivers in the RESPIRE group using a five-point Customer Satisfaction Score (CSAT). Ratings of 4 or 5 were classified as satisfied. The overall satisfaction rate was calculated as the number of caregivers reporting satisfaction divided by the total number of intervention participants, multiplied by 100. Higher percentages indicate greater satisfaction. | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 0
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|
Source 4
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.3.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 4a570df2e7274cee2d4fa2959402fab41880e2cd412e4b590390035fbea69391 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
Release trials-2026-11-12-0.3.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.