Theory of Mind in Preschool Children, School Children, Youths and Adults Born Preterm or Full-term
NCT ID: NCT02628015
Last Updated: 2016-03-14
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
480 participants
OBSERVATIONAL
2016-03-31
2018-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Psychomotor Performance of Preterm Infants
NCT05930522
Evaluation of Brain Plasticity in Premature Infants at School Age After Cognitive Remediation
NCT03972761
Associations Between General Movements Assessments and Cognitive Development
NCT05217056
Prematurity Related Risks of Cognitive Impairment at School Age
NCT02054507
Visual Maturation in Premature Newborns According to Factors Influencing Its Development
NCT02890251
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Four groups are tested: prescoolers (again two years later), youths and young adults.
All participants were tested for theory of mind, executive functions, language and cognitive abilites.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
CROSS_SECTIONAL
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
preschool children preterm
born 2010 or 2011 Birthweight \<1500g
No interventions assigned to this group
preschool children full-term
born 2010 or 2011 born after 38 weeks
No interventions assigned to this group
school children preterm
same children from the preschool group will be tested 2 years later again
No interventions assigned to this group
school children full-term
same children from the preschool group will be tested 2 years later again
No interventions assigned to this group
youths preterm
born 2001 or 2002 Birthweight \<1500g
No interventions assigned to this group
youths full-term
born 2001 or 2002 born after 38 weeks
No interventions assigned to this group
adults preterm
Birthweight \<1500g
No interventions assigned to this group
adults full-term
born after 38 weeks
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* preterm: birthweight \<1500g
* full-term: born after 38 weeks
Exclusion Criteria
4 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University Hospital of Cologne
OTHER
University of Bonn
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Stephanie Braun
Master of Science, Psychologist
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
University of Bonn
Bonn, , Germany
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
ToM-2016-2018
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.