Infant Development Clinical Trial
Official title:
A Randomized Crossover Study to Evaluate Differences Between the Bayley-II and the Bayley-III in Very Preterm Infants at 2 Years
NCT number | NCT01373177 |
Other study ID # | 10-007937 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | January 2011 |
Est. completion date | February 2015 |
Verified date | November 2019 |
Source | Children's Hospital of Philadelphia |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The objective of this randomized study is to test the hypothesis that scores on the Bayley Scales of Infant Development-III (Bayley-III) are higher than scores on the Bayley Scales of Infant Development-II (BSID-II) in the same group of infants who were born very preterm.
Status | Completed |
Enrollment | 119 |
Est. completion date | February 2015 |
Est. primary completion date | February 2015 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Months to 22 Months |
Eligibility |
Inclusion Criteria: - Birth weight <2000 grams and <32 weeks - Corrected age of 18-22 months. Exclusion Criteria: - English is not the primary language in the child's home. - Parent is unable to give informed consent for research participation. - Parent is unable to commit to returning for follow-up testing in 4-8 weeks. - Infant has severe medical illness or disability expected to impact his/her ability to participate in testing (ex: blindness, deafness, severe cerebral palsy, autism, tracheostomy). - No exclusion for economic status, gender, race or ethnicity. - Participation in a RCT that restricts timing and administration of developmental testing. |
Country | Name | City | State |
---|---|---|---|
United States | The Children's Hospital of Philadelphia | Philadelphia | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
Children's Hospital of Philadelphia | University of Pennsylvania |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The primary outcome is the mean difference between BSID-II Mental Development Index (MDI) and Bayley-III Cognitive Score. | 18-22 months | ||
Secondary | Mean difference between BSID-II Physical Development Index and Bayley-III Composite Motor Score. | 18-22 months | ||
Secondary | Proportion of infants classified as having "developmental delay" (MDI <70 on BSID-II or either Language or Cognitive Score <70 on the Bayley-III). | 18-22 months | ||
Secondary | The mean difference in scores between time point one and time point two (a measure of learning or training). | 18-22 months |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05793112 -
INF108F in Infants With Food Protein Induced Proctocolitis
|
Phase 4 | |
Recruiting |
NCT03828708 -
Early Iron Exposure on the Gut Microbiota in Young Infants
|
N/A | |
Recruiting |
NCT06018064 -
Investigating Fit and Satisfaction of the Prone Positioner
|
N/A | |
Not yet recruiting |
NCT06335524 -
Infant-Maternal Partnership and Cognitive Training Study for Preterm Infants
|
N/A | |
Not yet recruiting |
NCT05039918 -
Neonatal Experience of Social Touch
|
N/A | |
Completed |
NCT01166867 -
A Pilot Study Using Photo-plethysmographic (PPG) Camera
|
||
Completed |
NCT00791466 -
Maternal Iodine Supplementation and Effects on Thyroid Function and Child Development
|
N/A | |
Completed |
NCT03331276 -
Growth and Safety Study of an Infant Formula for Healthy Term Infants
|
N/A | |
Completed |
NCT05157633 -
Oral Exploration of Objects and Food Diversification
|
||
Completed |
NCT05217186 -
Associations Between Early Neonatal Neuroimaging, Hammersmith Infant Neurological Examination and General Movements
|
||
Recruiting |
NCT05006989 -
Blueberry Intake and Infant Gut Health
|
N/A | |
Completed |
NCT04901611 -
Parental Touch Trial (Petal)
|
N/A | |
Completed |
NCT03082313 -
Movement-based Infant Intervention
|
N/A | |
Recruiting |
NCT06053515 -
Rosie the Chatbot: Leveraging Automated and Personalized Health Information Communication
|
N/A | |
Completed |
NCT05394883 -
The SPROUT (Pilot) Project
|
N/A | |
Completed |
NCT03991949 -
Evaluation of Preterm Infants Fed Post-Discharge Preterm Infant Formula
|
N/A | |
Active, not recruiting |
NCT03851120 -
Brain Probiotic and LC-PUFA Intervention for Optimum Early Life
|
Phase 2 | |
Completed |
NCT03662048 -
Improving Infant Sleep Safety With the Electronic Health Record
|
N/A | |
Active, not recruiting |
NCT04749888 -
Impact of the Korea Early Childhood Home-visiting Intervention
|
N/A | |
Recruiting |
NCT06230848 -
Multisensory Early Oral Administration of Human Milk in Preterm Infants
|
N/A |