NCT07911228 Pediatric Research in the Outpatient Setting CoHort
| NCT ID | NCT07911228 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Insel Gruppe AG, University Hospital Bern |
| Condition | Parental Stress |
| Study Type | OBSERVATIONAL |
| Enrollment | 200 participants |
| Start Date | 2026-10-26 |
| Primary Completion | 2028-09-30 |
Eligibility & Interventions
Eligibility Fast-Check
Enter your details for a quick preliminary check. This does not replace medical advice.
What to Expect as a Participant
This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.
This trial targets 200 participants in total. It began in 2026-10-26 with a primary completion date of 2028-09-30.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
Though primary care pediatricians (PCPs) and general practitioners solve 90% of children's health problems without referral to specialized care (about 10% of total health expenditures) there is little data on the common health problems PCPs treat, mainly because pediatric primary care practices have little time to collect data and rarely have academic or administrative support to implement studies. We intend to create a digital pediatric cohort called Pediatric Research in the Outpatient Setting CoHort - PROS-CH (Switzerland), based on routine data collected with tablets using the digital data collection tool of REDCap. PCPs collect pediatric data from parents in practices' waiting rooms, and add their observations, treatment plans, and recommendations. To test the PROS-CH infrastructure's feasibility in pediatric practices under real-life conditions (pilot study), we will start with the following two pilot projects: 1) factors associated with a child's development of interaction and communication skills and measures taken; and 2) self-reported stress level of the parents of a newborn and measures taken.
Eligibility Criteria
Inclusion Criteria (all via Primary Care Pediatrician) : * All children aged \<2 at their first well-child visit Exclusion Criteria: * Declining the General Consent
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07911228 clinical trial?
This trial is open to participants of all sexes, studying Parental Stress. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07911228 currently recruiting?
Yes, NCT07911228 is actively recruiting participants. Contact the research team at julian.jakob@unibe.ch for enrollment information.
Where is the NCT07911228 trial being conducted?
This trial is being conducted at Bern, Switzerland.
Who is sponsoring the NCT07911228 clinical trial?
NCT07911228 is sponsored by Insel Gruppe AG, University Hospital Bern. The trial plans to enroll 200 participants.