Actively Recruiting

Phase Not Applicable
Age: 28Weeks - 34Weeks
All Genders
Healthy Volunteers
NCT06939192

E-health-supported Diagnostic and Intervention in Preterm Born Children and Their Families

Led by University Hospital Tuebingen · Updated on 2025-04-22

60

Participants Needed

1

Research Sites

152 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The app-based diagnostic and support approach with a focus on mental and somatic symptoms is intended to strengthen the resilience of premature born children and families and to identify risk and resilience factors.The overall objective of the study is to improve the post-inpatient care of families with premature born children. The procedure is evaluated by a two-arm design with an experimental group and a TAU group.

CONDITIONS

Official Title

E-health-supported Diagnostic and Intervention in Preterm Born Children and Their Families

Who Can Participate

Age: 28Weeks - 34Weeks
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Premature babies born at the UKT
  • Gestational age 28-34 weeks
  • Mother aged 18 years or older
  • Agreement to participate and signing of consent form
  • Sufficient knowledge of German
  • Access to the internet
Not Eligible

You will not qualify if you...

  • Premature babies born before 28 weeks or after 34 weeks of pregnancy
  • At least one child with serious nervous system diseases or obvious nervous disease symptoms
  • At least one child with serious congenital diseases or malformations
  • Mother lacks access to a smartphone or tablet
  • No internet access
  • Insufficient knowledge of German

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

University Hospital Tuebingen

Tübingen, Baden-Wurttemberg, Germany, 72076

Actively Recruiting

Loading map...

Research Team

A

Annette Conzelmann, Prof.Dr.

CONTACT

A

Annette Conzelmann, Prof. Dr.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here