Oliver Perra1,2, Sam Wass3, Alison McNulty4, David Sweet5, Kostas A Papageorgiou6, Matthew Johnston7,8,6, Delfina Bilello7,8,6, Fiona Alderdice9. 1. School of Nursing and Midwifery, Queen's University Belfast, Medical Biology Building, 97 Lisburn Road, Belfast, BT9 7BL, UK. o.perra@qub.ac.uk. 2. Centre for Evidence and Social Innovation, Queen's University Belfast, Medical Biology Centre, 97 Lisburn Road, Belfast, BT9 7BL, Northern Ireland, UK. o.perra@qub.ac.uk. 3. School of Psychology, University of East London, London, UK. 4. TinyLife, The Premature Baby Charity for Northern Ireland, Belfast, Northern Ireland, UK. 5. Health and Social Care Belfast Trust, Belfast, Northern Ireland, UK. 6. School of Psychology, Queen's University Belfast, Belfast, UK. 7. School of Nursing and Midwifery, Queen's University Belfast, Medical Biology Building, 97 Lisburn Road, Belfast, BT9 7BL, UK. 8. Centre for Evidence and Social Innovation, Queen's University Belfast, Medical Biology Centre, 97 Lisburn Road, Belfast, BT9 7BL, Northern Ireland, UK. 9. Nuffield Department of Population Health, University of Oxford, Oxford, UK.
Abstract
BACKGROUND:Very premature birth (gestational age between 28 and 31 + 6 weeks) is associated with increased risk of cognitive delay and attention deficit disorder, which have been linked to anomalies in the development of executive functions (EFs) and their precursors. In particular, very preterm (VP) infants display anomalies in controlling attention and gathering task-relevant information. Early interventions that support attention control may be pivotal in providing a secure base for VP children's later attainments. The Attention Control Training (ACT) is a cognitive training intervention that targets infants' abilities to select visual information according to varying task demands but had not been tested in VP infants. We conducted a feasibility study to test the processes we intend to use in a trial delivering the ACT to VP infants. METHODS AND DESIGN: We tested recruitment and retention of VP infants and their families in a randomised trial, as well as acceptability and completion of baseline and outcome measures. To evaluate these aims, we used descriptive quantitative statistics and qualitative methods to analyse feedback from infants' caregivers. We also investigated the quality of eye-tracking data collected and indicators of infants' engagement in the training, using descriptive statistics. RESULTS:Twelve VP infants were recruited, and 10 (83%) completed the study. Participants' parents had high education attainment. The rate of completion of baseline and outcome measures was optimal. VP infants demonstrated engagement in the training, completing on average 84 min of training over three visits, and displaying improved performance during this training. Eye-tracking data quality was moderate, but this did not interfere with infants' engagement in the training. DISCUSSION: The results suggest the ACT can be delivered to VP infants. However, challenges remain in recruitment of numerous and diverse samples. We discuss strategies to overcome these challenges informed by results of this study. TRIAL REGISTRATION: Registered Registration ID: NCT03896490 . Retrospectively registered at Clinical Trials Protocol Registration and Results System ( clinicaltrials.gov ).
RCT Entities:
BACKGROUND: Very premature birth (gestational age between 28 and 31 + 6 weeks) is associated with increased risk of cognitive delay and attention deficit disorder, which have been linked to anomalies in the development of executive functions (EFs) and their precursors. In particular, very preterm (VP) infants display anomalies in controlling attention and gathering task-relevant information. Early interventions that support attention control may be pivotal in providing a secure base for VPchildren's later attainments. The Attention Control Training (ACT) is a cognitive training intervention that targets infants' abilities to select visual information according to varying task demands but had not been tested in VPinfants. We conducted a feasibility study to test the processes we intend to use in a trial delivering the ACT to VPinfants. METHODS AND DESIGN: We tested recruitment and retention of VPinfants and their families in a randomised trial, as well as acceptability and completion of baseline and outcome measures. To evaluate these aims, we used descriptive quantitative statistics and qualitative methods to analyse feedback from infants' caregivers. We also investigated the quality of eye-tracking data collected and indicators of infants' engagement in the training, using descriptive statistics. RESULTS: Twelve VPinfants were recruited, and 10 (83%) completed the study. Participants' parents had high education attainment. The rate of completion of baseline and outcome measures was optimal. VPinfants demonstrated engagement in the training, completing on average 84 min of training over three visits, and displaying improved performance during this training. Eye-tracking data quality was moderate, but this did not interfere with infants' engagement in the training. DISCUSSION: The results suggest the ACT can be delivered to VPinfants. However, challenges remain in recruitment of numerous and diverse samples. We discuss strategies to overcome these challenges informed by results of this study. TRIAL REGISTRATION: Registered Registration ID: NCT03896490 . Retrospectively registered at Clinical Trials Protocol Registration and Results System ( clinicaltrials.gov ).
Authors: Peter J Anderson; Katherine J Lee; Gehan Roberts; Megan M Spencer-Smith; Deanne K Thompson; Marc L Seal; Chiara Nosarti; Andrea Grehan; Elisha K Josev; Susan Gathercole; Lex W Doyle; Leona Pascoe Journal: J Pediatr Date: 2018-08-31 Impact factor: 4.406
Authors: Oliver Perra; Fiona Alderdice; David Sweet; Alison McNulty; Matthew Johnston; Delfina Bilello; Kostas Papageorgiou; Sam Wass Journal: PLoS One Date: 2022-09-22 Impact factor: 3.752