- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT01807533
A Family-Centered Intervention Program for Preterm Infants: Effects and Their Biosocial Pathways
22 augusti 2018 uppdaterad av: National Taiwan University Hospital
Four hypotheses will be tested in this study:
- The intervention group performs better in child, parent and transactions outcomes than the control group throughout the follow-up period.
- The intervention group shows greater changes in early neurophysiological brain functions and transactions within the family that lead to better neurodevelopmental outcomes than the control group.
- Certain polymorphisms of the dopamine-related genes are associated with the neurodevelopmental outcomes in VLBW preterm infants.
- Very low birth weight preterm infants carrying more genetic plasticity in the dopamine-related genes may benefit more from the interventions than those carrying less genetic plasticity.
Studieöversikt
Status
Avslutad
Betingelser
Intervention / Behandling
Detaljerad beskrivning
A total of 275 VLBW preterm infants (269 participants and 6 pilots) were recruited at three medical centers in northern and southern Taiwan and were randomly assigned to the FCIP or UCP group.
Outcome assessments included primary (neurobehavioral development) and secondary measures (neurophysiological performance, parents' stress and transactions within the family).
The neurophysiological and transactions data were examined for whether they mediate intervention effects on child development.
In addition, these infants 219 VLBW preterm infants and 118 term infants in our prior intervention studies were collected buccal cells for assessment of the polymorphisms of dopamine-related genes, which are involved in the neurotransmission of cognitive, sensorimotor and behavioral-emotional systems and postulated to be associated with several developmental and psychiatric illnesses.
The polymorphisms of dopamine-related genes were examined for potential moderating influence on the effects of the intervention for child development.
Studietyp
Interventionell
Inskrivning (Faktisk)
275
Fas
- Inte tillämpbar
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
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Tainan, Taiwan, 704
- National Cheng Kung University Hospital
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Taipei, Taiwan, 100
- National Taiwan University Hospital
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Taipei, Taiwan, 104
- Mackay Memorial Hospital
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Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
Inte äldre än 8 månader (Barn)
Tar emot friska volontärer
Nej
Kön som är behöriga för studier
Allt
Beskrivning
Inclusion Criteria:
- birth body weight < 1500 grams
- gestational age < 37 weeks
- parents of Taiwan nationality, married or together at delivery, and northern family residing in greater Taipei and southern family residing in greater Tainan, Kaohsiung, or Chiayi
Exclusion Criteria:
- severe neonatal and perinatal diseases (e.g., seizures, hydrocephalus, meningitis, grade III-IV IVH and grade II NEC)
- congenital or chromosome abnormality
- mother < 18 years, with mental retardation or history of maternal substance abuse at any time (smoking, alcohol, and drug)
Terminated Criteria:
- diagnosis of brain injury (e.g., PVL, stage IV ROP or greater)
- severe cardiopulmonary disease requiring invasive or non-invasive ventilator use at hospital discharge
- hospital discharge beyond 44 weeks' post-menstrual age.
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Förebyggande
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Enda
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
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Experimentell: Family-centered intervention program
FCIP: family members were encouraged to present in all intervention sessions included 5 in-hospital intervention, 7 after-discharge interventions (0, 1, 2, 4, 6, 9, and 12 months of corrected age), and neonatal follow-up at 0, 1, 6, 12, 18, and 24 months of corrected age.
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This program was in-hospital intervention, after-discharge intervention, and neonatal follow-up.
Five sessions of in-hospital intervention emphasized in the parental involvements with modulation of the NICU, a teaching of child developmental skills, feeding support, massage, interactional activities, child developmental skills, parent support and education, and transition home preparation.
The 7-session after-discharge intervention consisted of 4 clinic visits and 3 home visits with specific care in modulation of home environment, teaching of child developmental skills, feeding support, teaching of interactional activities, and parent support and education
Andra namn:
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Övrig: Usual care intervention program
UCP: family members were invited to present at least one session of the 5 in-hospital intervention session.
Parents and infants in the UCP group received 7 after-discharge phone calls (0, 1, 2, 4, 6, 9, and 12 months of corrected age) and neonatal follow-up at 0, 1, 6, 12, 18, and 24 months of corrected age.
|
This program was in-hospital intervention, after-discharge consultation, and neonatal follow-up.
Five sessions of in-hospital intervention emphasized in the parental involvements with modulation of the NICU, a teaching of child developmental skills, feeding support, massage, interactional activities, child developmental skills, parent support and education, and transition home preparation.
The after-discharge service was provided 7-phone calls for the general health consultation.
Andra namn:
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
---|---|---|
Child: neurodevelopment functions (cognition, language and motor)
Tidsram: 24 months of corrected age
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Bayley Scales of Infant and Toddler Development - 2nd and 3rd edition
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24 months of corrected age
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Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
---|---|---|
Change of neurodevelopment functions (motor) from baseline
Tidsram: 0 months of corrected age
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The Neonatal Neurobehavioral Examination-Chinese Version (NNE-C) 2. World Health Organization Quality of Life- Brief Taiwan version
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0 months of corrected age
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Child: neurodevelopment functions (behavior)
Tidsram: 24 months of corrected age
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Child behavior checklist version 1.5-5 Y 2. World Health Organization Quality of Life- Brief Taiwan version
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24 months of corrected age
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Change of neurodevelopment functions (cognition, language and motor) from baseline
Tidsram: 6,12, and 24 months
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Bayley Scales of Infant and Toddler Development - 3rd edition 2. World Health Organization Quality of Life- Brief Taiwan version
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6,12, and 24 months
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Parental functions and change from baseline (pressure)
Tidsram: 0, 6, 12, 18, and 24 months of corrected age
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Parenting Stress Index 2. World Health Organization Quality of Life- Brief Taiwan version
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0, 6, 12, 18, and 24 months of corrected age
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Parental functions and change from baseline (Quality of Life)
Tidsram: 0, 6, 12, 18, and 24 months of corrected age
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World Health Organization Quality of Life- Brief Taiwan version
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0, 6, 12, 18, and 24 months of corrected age
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Transactional functions and change from baseline
Tidsram: 6, 12, and 18 months of corrected age
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Mother-infant interaction in free play at 6, 12, and 18 months of corrected age
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6, 12, and 18 months of corrected age
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Transactional functions and change from baseline
Tidsram: 6 and 12 months of corrected age
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Wakeful Position Questionnaire at 6 and 12 months of corrected age
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6 and 12 months of corrected age
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Transactions function: affordance
Tidsram: 18 months of corrected age
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1. Affordances in the Home Environment Motor Development- Chinese version
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18 months of corrected age
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Child: Medical data
Tidsram: Birth to 24 months of corrected age
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Chart review
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Birth to 24 months of corrected age
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Child: growth data and change from baseline
Tidsram: 0, 1, 4, 6, 12, 18, and 24 months of corrected age
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Chart review and measurement
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0, 1, 4, 6, 12, 18, and 24 months of corrected age
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Child: neurophysiological functions and change from baseline
Tidsram: 1 and 4 months of corrected age
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Electroencephalogram/event-related potential
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1 and 4 months of corrected age
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Child: genotyping and gene expression
Tidsram: 0 month of corrected age
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Buccal cell collection
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0 month of corrected age
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Parental adherence to Intervention
Tidsram: 32-36 weeks (5 sessions), 0, 1, 2, 4, 6, 9, and 12 months
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Only assessed in FCIP group
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32-36 weeks (5 sessions), 0, 1, 2, 4, 6, 9, and 12 months
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Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Samarbetspartners
Publikationer och användbara länkar
Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.
Allmänna publikationer
- Li SJ, Tsao PN, Tu YK, Hsieh WS, Yao NJ, Wu YT, Jeng SF. Cognitive and motor development in preterm children from 6 to 36 months of age: Trajectories, risk factors and predictability. Early Hum Dev. 2022 Sep;172:105634. doi: 10.1016/j.earlhumdev.2022.105634. Epub 2022 Jul 28.
- Yu YT, Huang WC, Hsieh WS, Chang JH, Lin CH, Hsieh S, Lu L, Yao NJ, Fan PC, Lee CL, Tu YK, Jeng SF. Family-Centered Care Enhanced Neonatal Neurophysiological Function in Preterm Infants: Randomized Controlled Trial. Phys Ther. 2019 Dec 16;99(12):1690-1702. doi: 10.1093/ptj/pzz120.
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart (Faktisk)
22 maj 2012
Primärt slutförande (Faktisk)
10 januari 2017
Avslutad studie (Faktisk)
10 januari 2017
Studieregistreringsdatum
Först inskickad
29 januari 2013
Först inskickad som uppfyllde QC-kriterierna
6 mars 2013
Första postat (Uppskatta)
8 mars 2013
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
24 augusti 2018
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
22 augusti 2018
Senast verifierad
1 mars 2017
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- 201103075RB
Plan för individuella deltagardata (IPD)
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